Digitale Landesbibliothek Berlin Logo
  • Show double pages

Diverse clinical spectrum of Niemann-Pick C: insights from a single center / Basan, Hacer (Rights reserved)

Access restriction

Eingeschränkter Zugang mit Nutzungsbeschränkungen: Das Dokument ist in den Räumen der Zentral- und Landesbibliothek mit dem "Virtuellen Lesesaal der Landesbibliothek" auf allen Internet-Arbeitsplätzen zugreifbar, darf jedoch nicht kopiert, versendet oder in einem Umfang von mehr als 10% ausgedruckt werden. Weitere Informationen.

Copyright

No licence for use has been granted - all rights reserved.

Bibliographic data

fullscreen : Diverse clinical spectrum of Niemann-Pick C: insights from a single center / Basan, Hacer (Rights reserved)

Access restriction

Eingeschränkter Zugang mit Nutzungsbeschränkungen: Das Dokument ist in den Räumen der Zentral- und Landesbibliothek mit dem "Virtuellen Lesesaal der Landesbibliothek" auf allen Internet-Arbeitsplätzen zugreifbar, darf jedoch nicht kopiert, versendet oder in einem Umfang von mehr als 10% ausgedruckt werden. Weitere Informationen.

Copyright

No licence for use has been granted - all rights reserved.

Files

Restricted access: The document can be accessed only at the computer workstations of the Zentral- and Landesbibliothek Berlin. Here you can find our current opening hours.

Unlock

Diverse clinical spectrum of Niemann-Pick C: insights from a single center / Basan, Hacer (Rights reserved)

You can request access to this file here. You will receive an e-mail confirming that we have successfully received your request.

Diverse clinical spectrum of Niemann-Pick C: insights from a single center / Basan, Hacer (Rights reserved)

The access to this file is restricted.

What color is the blue sky?:

I hereby confirm the use of my personal data within the context of the enquiry made.

Monograph

Title:
Verzeichnis der Friedlaenderschen Sammlung zur Geschichte der Bewegung von 1848 / Magistrats-Bibliothek zu Berlin
Other:
Magistratsbibliothek (Berlin). Friedlaendersche Sammlung
Publication:
Berlin: Wilhelm Baensch, 1897
Language:
German
Digitization:
Berlin: Zentral- und Landesbibliothek Berlin, 2021
Scope:
VI, 292 Seiten
Keywords:
Berlin ; Revolution ; Katalog
Berlin:
B 122 Geschichte: Revolution 1848
DDC Group:
943 Geschichte Deutschlands
URN:
urn:nbn:de:kobv:109-1-15435909
Collection:
History,Cultural History
Location:
Zentral- und Landesbibliothek Berlin
Shelfmark:
B 122/28
Copyright:
Public Domain
Accessibility:
Free Access
Title:
Verzeichnis der Friedlaenderschen Sammlung zur Geschichte der Bewegung von 1848 / Magistrats-Bibliothek zu Berlin
Other:
Magistratsbibliothek (Berlin). Friedlaendersche Sammlung
Publication:
Berlin: Wilhelm Baensch, 1897
Language:
German
Digitization:
Berlin: Zentral- und Landesbibliothek Berlin, 2021
Scope:
VI, 292 Seiten
Keywords:
Berlin ; Revolution ; Katalog
Berlin:
B 122 Geschichte: Revolution 1848
DDC Group:
943 Geschichte Deutschlands
URN:
urn:nbn:de:kobv:109-1-15435909
Collection:
History,Cultural History
Location:
Zentral- und Landesbibliothek Berlin
Shelfmark:
B 122/28
Copyright:
Public Domain
Accessibility:
Free Access

Chapter

Title:
E. Aus der Geschichte einzelner deutscher Staaten
Title:
E. Aus der Geschichte einzelner deutscher Staaten

Contents

Table of contents

  • The journal of pediatric endocrinology and metabolism (Rights reserved)
  • Molecular stability overrides size in giant pediatric pheochromocytoma / Simsek, Enver (Rights reserved)
  • A case report of Xp21 contiguous gene deletion syndrome with adrenal crisis and sensorineural hearing loss: clinical highlights and management pitfalls / Thangpong, Rungroj (Rights reserved)
  • Fresh frozen plasma as functional replacement therapy in early infantile ApoC-II deficiency: a molecularly confirmed case series / Ergun, Nurcan Üçüncü (Rights reserved)
  • Neonatal diabetes due to a truncating RFX6 mutation in an extremely low birth weight preterm infant with Mitchell–Riley syndrome / Mutlu, Birgul (Rights reserved)
  • Sterile abscesses during GnRH agonist therapy for central precocious puberty: a case series and literature review / Sarli, Walter Maria (CC BY)
  • Genotype–phenotype correlations in children with short stature: results of targeted next-generation sequencing / Meral, Rabia (Rights reserved)
  • Three cases of hereditary hypomagnesemia with secondary hypocalcemia caused by novel TRPM6 gene mutations and a literature review / Yang, Mengjie (Rights reserved)
  • Diverse clinical spectrum of Niemann-Pick C: insights from a single center / Basan, Hacer (Rights reserved)
  • Development of radiographic references for skeletal maturity in Indian children / Khadilkar, Vaman (Rights reserved)
  • Iodine status and thyroid function in children with multiple food allergy: a prospective cross-sectional study / Tekin, Suat (Rights reserved)
  • Changes in thyroid volume during the course of treatment of congenital primary hypothyroidism with an in situ thyroid gland / Yılmaz, Yunuscan (Rights reserved)
  • Overweight and obesity in youth with type 1 diabetes / Velasquez, H. Javier (Rights reserved)
  • Birth prevalence and characterisation of congenital hyperinsulinism in Western Australia over two decades / Stafford-Bell, Adam J. (Rights reserved)
  • Continuous glucose monitoring characteristics of common MODY subtypes and their clinical applications: a review / Rouzimaimaiti, Aibibai (Rights reserved)
  • Frontmatter (Rights reserved)
  • Successful desensitization to alglucosidase alfa in a very young infant with Pompe disease / Aytekin Güvenir, Funda (Rights reserved)
  • Erratum to: Reliability of point-of-care glucose in neonates: revisiting hypoglycemia protocols in the NICU / Hamama, Ibrahim (Rights reserved)
  • Nine-year cinacalcet monotherapy in a child with neonatal severe hyperparathyroidism caused by compound heterozygous CASR mutations / Roztoczyńska, Dorota (CC BY)
  • Challenges of pediatric ectopic ACTH syndrome from sacrococcygeal teratoma / Che, Ruochen (Rights reserved)
  • A novel PAPSS2 pathogenic variant: expanding the mutational spectrum and genotype–phenotype landscape in skeletal dysplasia / Sarıkaya Özdemir, Behiye (Rights reserved)
  • Genotype–phenotype associations of MKRN 3 variants in children with central precocious puberty: a single-center study from Uzbekistan / Khalimova, Zamira Yusufovna (Rights reserved)
  • ˜Theœ silent threat in mucopolysaccharidosis: assessment of sleep quality and disorders / Çakar, Nafiye Emel (Rights reserved)
  • Steroid profiling in congenital adrenal hyperplasia: comparing immunoassays and LC-MS/MS accuracy / Taba-Tabai, Shahla (Rights reserved)
  • Factors affecting the success of follow-up and treatment of adults with phenylketonuria diagnosed by newborn screening / Tandoğan, Zelal (CC BY)
  • Investigating thyroid dysfunction in pediatric patients following the administration of iodinated contrast media during cardiac catheterization / Lindsey, William Wyatt (Rights reserved)
  • Evaluating the transition of young adults with osteogenesis imperfecta: a patient-focused prospective study / Collins, Lucy (CC BY)
  • Two-year follow-up of musculoskeletal outcomes and quality of life in patients with mucopolysaccharidosis type IV and VI / Genç, Emine (Rights reserved)
  • Evaluation of the relationship between HOMA-IR, triglyceride-glucose index, and triglyceride/HDL-cholesterol ratio with the presence and severity of hepatic steatosis in children with obesity / Turan, Benay (Rights reserved)
  • Larks vs. owls: exploring chronotype, glycaemic control, and quality of life in paediatric type 1 diabetes / Aydın, Dilek Bingöl (Rights reserved)
  • Frontmatter (Rights reserved)
  • Childhood thiamine-responsive megaloblastic anemia and diabetes: a case series highlighting early diagnosis and management / Yılmaz, Uğur Cem (CC BY)
  • A case of Alström syndrome with growth hormone deficiency and dyslipidemia: a novel homozygous frameshift variant of ALMS1 c.5763del / Goda, Takeshi (Rights reserved)
  • A rare case of severe short stature diagnosed after late-onset hypocalcemia: Kenny–Caffey syndrome type 2 / Özer, Gülşen (Rights reserved)
  • Xq27.3–q28 duplication involving the FMR1 gene presenting with familial X-linked hypogonadism, gynecomastia, short stature, intellectual disability, and obesity syndrome: a case report and review of the literature / Oktay, Mehmet Ali (CC BY)
  • Presumptive ovarian hyperthecosis in an adolescent girl with sustained remission after oral contraceptive therapy: a 23-year follow-up case report / Frank, Graeme R. (Rights reserved)
  • Clinical course of Graves’ orbitopathy in children with newly diagnosed hyperthyroidism: a prospective observational study / Tepe, Derya (Rights reserved)
  • Maternal β-hCG and neonatal hormone profiles as predictors of anogenital distance: assessing the fetal reproductive axis / Mishra, Ipsita (Rights reserved)
  • A comparative analysis of all reported patients with MTHFS-related neurodevelopmental disorder / Kılıç, Mustafa (Rights reserved)
  • Parent-perceived stressors and stress-dosing practices during suspected adrenal crisis in children with congenital adrenal hyperplasia: a cross-sectional, parent-reported study / Cubberley, Sarah K. (Rights reserved)
  • Clinical characteristics and endocrine outcomes of functional and nonfunctional adrenal lesions in children: a single-center cohort study / Deligozoglu, Duygu (Rights reserved)
  • Are children with inborn errors of metabolism and cystic fibrosis adequately protected? Immunization status and seroepidemiological evaluation of vaccine-preventable diseases / Kılıç Yıldırım, Gonca (Rights reserved)
  • Early metabolic and hepatic alterations in children with Down syndrome: a hidden risk beyond BMI / Calcaterra, Valeria (CC BY)
  • Beyond A 1c: a narrative review of mental health integration in pediatric type 1 diabetes care / Jetter, Ethan (Rights reserved)
  • Frontmatter (Rights reserved)
  • New insights into Oliver–McFarlane syndrome: adrenocortical hypofunction and variable expressivity in a Chinese sibling pair / Du, Caiqi (Rights reserved)
  • Corrigendum to: Family and culture in type 1 diabetes transition care: a mini review / Kelleher, Jennifer A. (Rights reserved)
  • A rare coexistence: tyrosinemia type III and Wolff–Parkinson–White syndrome / Yılmaz-Gümüş, Emel (Rights reserved)
  • Pituitary dysfunction in childhood after (177 Lu) Lu-DOTATATE therapy / van Wessel, Karen (CC BY)
  • Endocrine and metabolic features of PTEN hamartoma tumor syndrome in childhood: a pediatric case series / Özsoy, Nazlı Sultan (Rights reserved)
  • Is mild citrullinemia type I truly benign? a study of long-term clinical outcomes / İşler-Soylu, Elif (CC BY)
  • Age and sexual maturation at Spermarche in boys with Laron syndrome / Laron, Zvi (Rights reserved)
  • Selective neuroanatomical alterations in children with growth hormone deficiency: a volumetric MRI analysis using automated segmentation / Özyılmaz, Safa (Rights reserved)
  • Genetic evaluation of a group of patients with transient congenital hypothyroidism by targeted exome sequencing / Köprülü, Özge (Rights reserved)
  • Serum selenium levels in children and adolescents with Hashimoto’s thyroiditis: a cross-sectional case–control study / Kara, Esra (Rights reserved)
  • Associations of personal solar UV exposure with gut microbiota diversity and BMI among preschool children in China / Liang, Jiawen (Rights reserved)
  • Predicting abdominal obesity in children and adolescents via machine learning: a longitudinal cohort study / Ding, Xiaoyan (Rights reserved)
  • Digital biomarkers of pediatric metabolic health in children with obesity: insights from wearable-derived heart rate data / Bosoni, Pietro (CC BY)
  • Reliability of point-of-care glucose in neonates: revisiting hypoglycemia protocols in the NICU / Hamama, Ibrahim (Rights reserved)
  • Report on the 2nd Conference of the German Society for Paediatric and Adolescent Endocrinology and Diabetology (DGPAED) in Leipzig/Halle, Saale 2025 / Kapellen, Thomas Michael (Rights reserved)
  • Frontmatter (Rights reserved)
  • Comment on “Exploratory real-world experience with glucagon-like peptide 1 receptor agonists vs. metformin in youth with new-onset type 2 diabetes: a single-center retrospective study” / Sundar Sah, Shyam (Rights reserved)
  • ˜Theœ clinical picture of symptomatic Rathke cleft cysts in children / Cebeci, Ayse Nurcan (Rights reserved)
  • Response to comment on “Exploratory real-world experience with GLP-1 receptor agonists vs. metformin in youth with new-onset type 2 diabetes: a single-center retrospective study” / Zeier, Troy (CC BY)
  • Dyggve–Melchior–Clausen syndrome in three siblings: a unique case series with dual diagnosis of Down syndrome and Hirschsprung disease / Halis, Meryem (Rights reserved)
  • Severe metabolic acidosis in succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: case report of a novel pathogenic OXCT1 variant (L131_E132dup) and its pathophysiological basis / Adachi, Natsuho (Rights reserved)
  • LRP5 -related primary osteoporosis: phenotypic spectrum and treatment response to zoledronic acid / Balagamage, Chamila (Rights reserved)
  • 46,XY differences of sex development in pontocerebellar hypoplasia type 7 (PCH7): two case reports and systematic review / Pachapure, Shaila Sanjay (Rights reserved)
  • GATA4 gene variants in 46,XY differences of sex development: report of four cases and literature review / Mansó Borràs, Maria (Rights reserved)
  • Cardiac involvement across mucopolysaccharidosis subtypes: insights from a longitudinal single-center study / Borakay, Dilek (Rights reserved)
  • Automatic bone age assessment for adult height prediction in children with congenital adrenal hyperplasia / Çetin, Kürşat (Rights reserved)
  • Evaluation of male reproductive function after aromatase inhibitor treatment during adolescence: case series with literature review / Dai, Chengjun (CC BY)
  • Psychosocial adaptation of parents of children with type 1 diabetes: a cross-sectional study / Öztürk, İlayda Şenol (Rights reserved)
  • Clinical characteristics and risk factors of patients with cystic fibrosis-related diabetes and pre-diabetes: cohort of cystic fibrosis registry of Türkiye / Özaslan, Mehmet Mustafa (CC BY)
  • Effect of androgens on retinal microvasculature in prepubertal girls with isolated premature pubarche / Karataş, Gamze (Rights reserved)
  • Puberty promoting low dose testosterone treatment improved wellbeing and emotional state in boys with self-limited delayed puberty / Österbrand, Martin (CC BY)
  • Clinical evidence, practical contradictions, and monitoring of rhGH-assisted height enhancement in children with CAH / Zhao, Ying (Rights reserved)
  • Frontmatter (Rights reserved)
  • Berardinelli–Seip congenital lipodystrophy type-2: a case series of three Indian children / Gyani, Surbhi (Rights reserved)
  • Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED): a case series and experience from a UK tertiary paediatric hospital / Baioumi, Alaa (CC BY)
  • A novel CEP57 gene mutation in mosaic variegated aneuploidy syndrome 2: case report / Viudes, Cristina Pellicer (Rights reserved)
  • Meier–Gorlin syndrome due to a recurrent DONSON variant in a Turkish family: first report of thumb aplasia and long-term growth data / Sezer, Abdullah (Rights reserved)
  • Hypertrophic cardiomyopathy as a novel phenotypic feature of NSUN3 -related mitochondrial disease: a case report with review of the literature / Şenol Ersak, Ayşe (Rights reserved)
  • Long-term outcomes in ovotesticular DSD: insights from a single-centre Indian cohort / Mehta, Niragi (Rights reserved)
  • Association of MC4R rs17782313 and multi-locus genetic variants with metabolic syndrome in Northern Vietnamese children aged 6–11 years: an exploratory study / Nguyen, Thi Hong Hanh (Rights reserved)
  • ˜Theœ prevalence of autoimmune diseases in antibody negative type 1 diabetes mellitus / Bakjaji, Shadi (Rights reserved)
  • Bone age advancement in non-obese children with premature adrenarche: relationship to growth acceleration and predicted adult height outcomes / Çiftci, Nurdan (Rights reserved)
  • Pediatric thyroid cancer lung metastases and RAI: long-term results / Mueller, Ryan C. (CC BY)
  • Volumetric MRI assessment of brain and pituitary structure in girls with central precocious puberty / Özyılmaz, Safa (Rights reserved)
  • Family and culture in type 1 diabetes transition care: a mini review / Kelleher, Jennifer A. (Rights reserved)
  • Frontmatter (Rights reserved)
  • Potential mechanistic role of the liver-thyroid axis in clinical manifestations of kwashiorkor / Linneman, Zachary (Rights reserved)
  • Tolvaptan: a potential rescue therapy for SIADH with refractory hyponatremia associated with acute intermittent porphyria / Gupta, Rahul (Rights reserved)
  • Rare phenotypic spectrum of 17β-hydroxysteroid dehydrogenase 3 deficiency: case series from infancy to adolescence / Sridhar, Subbiah (Rights reserved)
  • Thyroid hormone metabolism defect due to compound heterozygous SECISBP2 mutations: first reported case in Korea / Yang, Jina (CC BY)
  • ˜Theœ first report of a gross deletion in the SCNN1G gene in a case presenting with hyponatremic convulsion at fifth year of treatment / Bolaç Özyılmaz, Leyla Gizem (Rights reserved)
  • Diagnostic pitfalls in aldosterone defects: a 9-year follow-up of early-onset pseudohypoaldosteronism type 2 / Cay, Mevra (Rights reserved)
  • Efficacy and outcomes of 6-month triptorelin formulation in girls treated for central precocious puberty for 24 months and beyond / Foreman, Allison (CC BY)
  • A rare metabolic cause of premature ovarian insufficiency: case report of transaldolase deficiency / Köprülü, Özge (Rights reserved)
  • Evaluation of adrenomedullin levels in adolescents with Hashimoto’s thyroiditis: association with clinical and laboratory findings / Cambaz Kurt, Nevin (Rights reserved)
  • Suboptimal adoption of diabetes technology despite coverage and the impact on glycemic outcomes in children and adolescents with type 1 diabetes in Hong Kong / Poon, Sarah Wing-yiu (Rights reserved)
  • Impact of continuous glucose monitoring on fear of hypoglycemia and quality of life in children and adolescents with type 1 diabetes / Köprülü, Özge (Rights reserved)
  • Customized birth weight percentiles for identification of SGA short statue / Held, Corinna Melanie (Rights reserved)
  • Efficacy, adherence, and cost-efficiency of three growth hormone treatment strategies in children with idiopathic short stature: a retrospective cohort study / Jie, Li (CC BY)
  • Impact of eating behaviour on craniopharyngioma-associated obesity / Eddy, Danielle (CC BY)
  • Frontmatter (Rights reserved)
  • Management of porphyria-like syndrome in tyrosinemia type 1 / Basan, Hacer (Rights reserved)
  • A 2-year-old girl with merged phenotypes: galactosemia and Coffin–Lowry syndrome / Sayar, Esra (Rights reserved)
  • Phosphoglucomutase 1 deficiency misdiagnosed as Laron syndrome / Uçaktürk, Seyit Ahmet (Rights reserved)
  • Positive neonatal screening test for congenital adrenal hyperplasia in a case with 3β-hydroxysteroid dehydrogenase type 2 deficiency / Anik, Merve (Rights reserved)
  • Glutathione synthetase deficiency: severe hemolysis and metabolic acidosis with symptoms in the intrauterine period / Demirsu, Aysegul (Rights reserved)
  • Knowledge of advanced carbohydrate counting in children and adolescents with type 1 diabetes and its effect on glycaemic control / Alassaf, Abeer (Rights reserved)
  • Cataract in children with type 1 diabetes: a single-center experience from North India on an underrecognized complication / Dayal, Devi (Rights reserved)
  • GLP-1 receptor agonists reduce body mass index and total daily insulin dose in youth with type 1 diabetes: a retrospective cohort study / Gonzalez, Frances (CC BY)
  • ˜Theœ incidence of sellar abnormalities in newly diagnosed children with central precocious puberty: a single-center study based on 625 cases / Shi, Wen-Hui (Rights reserved)
  • Can uric acid levels be helpful for the diagnosis of CPP in girls? / Singin, Berna (Rights reserved)
  • Is the tracheal index useful for evaluating the thyroid in infants suspected of hypothyroidism? / Muratoglu Sahin, Nursel (Rights reserved)
  • Evaluation of children with solid thyroid nodules: a single-center experience / Günbey, Ömer (CC BY)
  • A comparative study of the interpretation results of different artificial intelligence bone age assessment software / He, Jinshui (Rights reserved)
  • Do patients with idiopathic short stature or partial growth hormone deficiency need to continue growth hormone therapy during puberty? / Cantas-Orsdemir, Sena (Rights reserved)
  • Effects of exercise training on cardiorespiratory fitness in children and adolescents with overweight or obesity: a systematic review / Cao, Youxiang (Rights reserved)
  • Frontmatter (Rights reserved)
  • Wolcott–Rallison syndrome due to a novel homozygous missense variation (p.Gly602Val) in the exon 11 of EIF2AK3 gene / Gaur, Bablu Kumar (Rights reserved)
  • Clinical insights of the TBX19 C.856 C>T variant: a case report and literature review on neonatal isolated ACTH deficiency / Kizilcan Cetin, Sirmen (CC BY)
  • Novel MCT8 mutation: diagnostic value of T3/T4 ratio / Laaraje, Azzeddine (Rights reserved)
  • Adrenal oncocytoma: an unusual etiology of Cushing’s syndrome in an adolescent female / Memon, Saba Samad (Rights reserved)
  • Noonan syndrome and autoimmune hepatitis: patient report and literature review / Pescini, Aurora (Rights reserved)
  • Implementation and feasibility of a nutrition assessment for recently diagnosed youth with type 2 diabetes / Wu, Charles (Rights reserved)
  • Characterization of monogenic diabetes among Sudanese children: a multi-center experience from a population with high consanguinity / Hassan, Samar S. (Rights reserved)
  • Exploratory real-world experience with GLP-1 receptor agonists vs. metformin in youth with new-onset type 2 diabetes: a single-center retrospective study / Tejeji, Isaac (CC BY)
  • ˜Theœ impact of hepatic steatosis on epicardial adipose tissue in obese individuals / Trabzon, Gül (Rights reserved)
  • Role of hyperandrogenism on disordered eating behaviors in adolescents with PCOS and interplay with insulin resistance / Kaymaz, Nazan (Rights reserved)
  • ˜Theœ relationship between FSTL-1 (follistatin-related protein 1), FAM19A5 (family with sequence similarity 19, member A5) and CTRP-6 (C1q/TNF-related protein 6) levels and metabolic parameters in overweight children / Can, Fatmagül (Rights reserved)
  • Bioelectrical impedance analysis and hormonal assessment in adolescents with pubertal gynecomastia / Kırkgöz, Tarık (Rights reserved)
  • Serum α-Klotho and its association with testosterone in boys with central precocious puberty / Noh, Eu-seon (CC BY)
  • Pubertal characteristics, final height, and associated factors in patients with nonclassical congenital adrenal hyperplasia: a single center experience / Abseyi, Sema Nilay (CC BY)
  • Frontmatter (Rights reserved)
  • Prevalence of congenital hypothyroidism in infants of mothers with hypothyroidism: a meta-analysis / Yarlagadda, Shree Dheera (Rights reserved)
  • Pseudohypertriglyceridemia as a clue: clinical and genetic spectrum of glycerol kinase deficiency in three pediatric cases / Kara, Cemre (CC BY)
  • Effective treatment of hyperphosphatemia with denosumab in patients with loss of function of FGF23 and high bone density: case series / Vafadar, Mehdi (Rights reserved)
  • Family experience with individuals of different ages and clinical presentations diagnosed with DI: do familial DI cases tolerate polyuria better? / Birinci, Hakan (Rights reserved)
  • Prognostic analysis of persistent disease in medium-to high-risk children and adolescents with differentiated thyroid carcinoma / Liang, Huanxin (Rights reserved)
  • Cognitive behavioral therapy (CBT) effect on diabetic youth depression, death anxiety and glycemic control / Khleif, Mohamad H. (Rights reserved)
  • Reviewer Acknowledgment (Rights reserved)
  • Maturity-onset diabetes of the young due to HNF1β variants (HNF1β -MODY): a 2-year follow-up study of six patients from a single diabetes center / Jiang, Handan (Rights reserved)
  • Pitfalls in the diagnosis of carnitine palmitoyltransferase 1 deficiency / Grünert, Sarah C. (Rights reserved)
  • Dual molecular genetic diagnosis with combined malonic and methylmalonic aciduria (CMAMMA): implications of coexisting genetic disorders on clinical presentation / Ersoy, Melike (Rights reserved)
  • ˜Theœ clinical picture of symptomatic Rathke cleft cysts in children / Cebeci, Ayse Nurcan (Rights reserved)
  • Transient worsening of thyrotoxic myopathy following methimazole and metoprolol initiation in a 12-year-old girl: a case report and literature review / Onishi, Yuto (Rights reserved)
  • Atypical pediatric presentation of hyperparathyroidism: CDC73 gene mutation and parathyroid carcinoma / Aytaç Kaplan, Emel Hatun (Rights reserved)
  • Investigating the kynurenine pathway in pediatric metabolic health / Özgüç Çömlek, Fatma (Rights reserved)
  • Mucolipidosis type II and III: clinical spectrum, genetic landscape, and longitudinal outcomes in a pediatric cohort with six novel mutations / Erdem, Fehime (CC BY)
  • Subclinical but significant? Updated review of pediatric hypothyroidism / Cooper, Felicia (Rights reserved)
  • ˜Theœ differential impact of automated insulin delivery systems on body mass index in children with type 1 diabetes / Pemberton, John (CC BY)
  • Evaluation of the genetic alterations landscape of differentiated thyroid cancer in children / Çetiner, Ebru Barsal (Rights reserved)
  • Frontmatter (Rights reserved)
  • Real-world effectiveness of sodium glucose transporter 2 inhibitors among youth with type 2 diabetes / Timkovski, Michal (Rights reserved)
  • Causal analysis of uterine artery pulsatility index-related proteins and the risk of precocious puberty in girls: a Mendelian randomization study / Gao, Yi (Rights reserved)
  • Spatiotemporal associations between incidence of type 1 diabetes and COVID-19 vaccination rates in children in Germany – a population-based ecological study / Kamrath, Clemens (CC BY)
  • Investigation of the association between nitric oxide synthase gene variants and NAFLD in adolescents with obesity / Hasanoğlu Sayın, Sevde (Rights reserved)
  • Understanding rickets in osteopetrosis via a case: mechanisms and treatment implications / Bilici, Meliha Esra (Rights reserved)
  • A disease that is difficult to predict: regional distribution and phenotypic, histopathological and genetic findings in McArdle disease / Erdoğan, Bahattin (Rights reserved)
  • Annual case counts and clinical characteristics of pediatric and adolescent patients with diabetes in Kenyatta National Hospital, Nairobi, Kenya. A 14 year retrospective study / Wamalwa, Phoebe (Rights reserved)
  • Compound heterozygous ROBO1 gene variants in a neonate with congenital hypopituitarism, dysmorphic features and midline abnormalities: a case report and review of the literature / Markopoulou, Panagiota (CC BY)
  • Immunogenetic profiling of type 1 diabetes in Jordan: a case-control study on HLA-associated risk and protection / Odeh, Rasha (Rights reserved)
  • MMP13-related metaphyseal dysplasia: a differential diagnosis of rickets / Kolkiran, Abdulkerim (Rights reserved)
  • Impact of race and delayed adoption of diabetes technology on glycemia and partial remission in type 1 diabetes / Chader-Gata Garcia, Adriana (CC BY)
  • Continuous glucose monitoring evidence of celiac disease in type 1 diabetes / Ruiz, Jessica L. (CC BY)
  • Cardiometabolic outcomes in girls with premature adrenarche: a longitudinal analysis of typical vs. exaggerated presentations / Seymen, Gülcan (Rights reserved)
  • Phenotypic variation among four members in a family with DAX1 deficiency / Seki, Yuko (Rights reserved)
  • A case of JAGN1 mutation presenting with atypical diabetes and immunodeficiency / De Cuyper, Céline (Rights reserved)
  • JA-PED | Annual Meeting of the German Society for Pediatric and Adolescent Endocrinology and Diabetology (DGPAED e. V.) (Rights reserved)
  • Frontmatter (Rights reserved)
  • Surgical treatment and somatostatin experience in growth hormone-secreting pituitary macroadenoma due to novel AIP mutation / Karagöz, Kıymet (Rights reserved)
  • Identification of pathogenic ACAN variants in healthy children with normal height and advanced bone age / Hernández, María Isabel (Rights reserved)
  • ANKS1B is a potential candidate gene for short stature and failure to thrive in children / Prasun, Pankaj (Rights reserved)
  • Hashimoto’s thyroiditis in children and adolescents: analysis of long-term course / Ayşe Yaşar (Rights reserved)
  • First evaluation of fibroblast growth factor 21 levels in patients diagnosed with glycogen storage diseases with liver involvement / Bozkurt, Abdullah (Rights reserved)
  • Impact of high-dose vitamin D supplementation initiated shortly after diagnosis on residual beta cell function and partial remission rates in children with type 1 diabetes / Nallapu, Chandan (Rights reserved)
  • 45, X/46, XY mosaicism and gender incongruence: ethical, medical, and psychological considerations / Horrigan, Charlotte (Rights reserved)
  • Clinical spectrum, imaging characteristics, and treatment outcomes of pediatric adrenocortical tumors: a 24-year experience from Western India / Daga, Aaditya (Rights reserved)
  • Hormone-active ovarian steroid cell tumor in a 2-year-old girl / Weihrauch-Blüher, Susann (Rights reserved)
  • Improving cardiometabolic health in children and adolescents with obesity: a comparison between in-person and virtual supervised training / Calcaterra, Valeria (CC BY)
  • Concerns for mood disorders in children presenting with early menarche is not an indication for pubertal suppression / Acinikli, Kübra Yüksek (Rights reserved)
  • Lipoatrophy following weekly growth hormone therapy: a case report / Hazer, Ilhan (Rights reserved)
  • Comparison study of the correlation between free and total 25 (OH) D in maternal and umbilical blood and early-life physical development parameters / Tian, Zhihong (Rights reserved)
  • A multi-stakeholder perspective on medical devices for children and adolescents with type 1 diabetes: huge unmet needs for the smallest / Biester, Torben (Rights reserved)
  • Testosterone in Duchenne muscular dystrophy: effects on puberty and growth / McCauley, Cara (Rights reserved)
  • Frontmatter (Rights reserved)
  • Testicular adrenal rest tumors in Indonesian boys with congenital adrenal hyperplasia / Chandra, Epifani A. (Rights reserved)
  • Pediatric iatrogenic Cushing’s syndrome: a series of seven cases induced by topical corticosteroid use / Kilci, Fatih (Rights reserved)
  • Frontmatter (Rights reserved)
  • Delayed diagnosis of retroperitoneal paraganglioma in an 8-year-old boy with persistent hypertension: a case report and review of diagnostic challenges in pediatric secondary hypertension / Pan, Dongxue (Rights reserved)
  • Characterizing the metabolome of children with growth hormone deficiency / Shilo, Smadar (CC BY)
  • Pubertal induction therapy in pediatric patients with Duchenne muscular dystrophy / Sodero, Giorgio (Rights reserved)
  • Biological effects of recombinant human growth hormone therapy on metabolism in children with growth hormone deficiency: a review / Dyrka, Kamil (Rights reserved)
  • Comparison of the clinical characteristics of children with Silver–Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study / Özgen, İlker Tolga (Rights reserved)
  • Endocrine treatment in Duchenne muscular dystrophy – current practices and future directions / Pechmann, Astrid (Rights reserved)
  • ˜Theœ use of bisphosphonate and testosterone in young people with Duchenne muscular dystrophy: an international clinician survey / McCarrison, Sarah (Rights reserved)
  • Is L-dopa test effective in detecting adrenal insufficiency with preliminary diagnosis of growth hormone deficiency in children with short stature? / Vural Topaktaş, Gülümay (Rights reserved)
  • Evaluating obesity and fat cells as possible important metabolic players in childhood leukemia / Sallati, Isabela (Rights reserved)
  • Wolcott–Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure – a case report / Teke, Selçuk (Rights reserved)
  • Oxidative stress in branched-chain organic acidemias using thiol-disulfide homeostasis / Göksoy, Emine (Rights reserved)
  • Prolonged symptom duration and the potential for gradual progression in pediatric adrenocortical tumors: observations from the MET studies / Kuhlen, Michaela (Rights reserved)
  • Height velocity in the detection of growth disorders reconsidered: a retrospective analysis of the DONALD study / Duran, Ibrahim (Rights reserved)
  • 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: case report of a child with rare HMGCL gene variants / Bjelica, Milena (Rights reserved)
  • ˜Theœ diagnostic value of stimulated androgen ratios in 5-alpha reductase type 2 (SRD5A2) deficiency: a case series and review of the literature / Balagamage, Chamila (CC BY)
  • ˜Theœ diagnostic utility of bioelectrical impedance analysis in distinguishing precocious puberty from premature thelarche / Koca, Serkan Bilge (Rights reserved)
  • Genetic, neuroimaging, and clinical characteristics of a cohort of individuals with L-2-hydroxyglutaric aciduria from Türkiye / Engin Erdal, Ayşenur (Rights reserved)
  • Distinguishing organic from idiopathic central precocious puberty: clinical characteristics and predictive factors for organic etiology in a multicenter Italian cohort study / Sodero, Giorgio (Rights reserved)
  • Evaluation of thyrotrophic and lactotrophic reserves in patients with pituitary dwarfism with and without empty sella turcica / Geremia, César (Rights reserved)
  • Stress hyperglycemia in pediatric patients as a risk factor for type 1 diabetes – a single center experience / Weiser, Giora (Rights reserved)
  • Observations of the effect of gonadotropin-releasing hormone analog treatment on psychosocial well-being in transgender youth and their caregivers – a pilot study / Gohil, Anisha (Rights reserved)
  • Transition of care from childhood/adolescence to adulthood in familial hypercholesterolemia / Maia, Ariana (Rights reserved)
  • Frontmatter (Rights reserved)
  • Rare pediatric insulinoma case diagnosed by endoscopic ultrasonography: insights into endogenous hyperinsulinemic hypoglycemia / Bilici, Meliha Esra (Rights reserved)
  • Caudal epidural steroid injection as a novel therapy for treatment-induced neuropathy of diabetes in children: report of two cases / Bala, Anju (Rights reserved)
  • Differentiating transient and permanent congenital hypothyroidism: predictive clues from Istanbul, Türkiye / Ulusoy, Ceren (Rights reserved)
  • Performance of adult height prediction methods in 6 to 8-year-old girls with GnRH-dependent precocious puberty / Erkko, Anni (Rights reserved)
  • GNB1 haploinsufficiency presents as monogenic obesity syndrome / Prasun, Pankaj (Rights reserved)
  • Exploring the impact of androgen levels on depression and anxiety in adolescent females: a clinical perspective / Aytaç Kaplan, Emel Hatun (Rights reserved)
  • A novel homozygous missense DNAJC3 variant in syndromic juvenile-onset diabetes / Mengen, Eda (Rights reserved)
  • Endocrinopathies associated with pediatric common variable immunodeficiency / Neneman, Jan (Rights reserved)
  • Association between overweight or obesity and vitamin D status in preschool children: an epidemiological survey in Beijing, China, 2021–2023 / Yuan, Li (Rights reserved)
  • ˜Theœ clinical presentation and genetic diagnosis of Tangier disease in the pediatric age group / Öztürk, Selcan (Rights reserved)
  • Body composition assessment measured via bioelectrical impedance analysis in euthyroid children with newly diagnosed Hashimoto’s thyroiditis / Koca, Serkan Bilge (Rights reserved)
  • Relationships among biological sex, body composition, and bone mineral density in young persons with and without diabetes / Platnick, Carson (Rights reserved)
  • Sialidosis type 1 in a Turkish family: a case report and review of literatures / Kılıç, Mustafa (Rights reserved)
  • ˜Theœ changing landscape in the evaluation of hypotonic polyuria in children and adolescents: the role of the new copeptin stimulation tests / Garibaldi, Luigi R. (CC BY)
  • Association between partial remission phase in type 1 diabetes and vitamin D receptor Fok1 rs2228570 polymorphism / Masoud, Randa Mahmoud (Rights reserved)
  • Influence of excess weight on metabolic risk factors in Argentinian preschool children / Malpeli, Agustina (Rights reserved)
  • Frontmatter (Rights reserved)
  • Thyroid surgery in pediatric age: a 10-year experience at a single center and literature review / Asya, Orhan (Rights reserved)
  • Evaluation of iodine and selenium level and thyroid functions in patients with cystic fibrosis / Unal, Edip (Rights reserved)
  • Reninoma: an unusual cause of growth failure / Vaghasia, Nupoor (Rights reserved)
  • Does clonidine stimulate copeptin in children? / Binder, Gerhard (Rights reserved)
  • Physical activity and vitamin D in children: a review of impacts on bone health and fitness / Devulapalli, Chandra Sekhar (Rights reserved)
  • Early-onset growth hormone treatment in Prader–Willi syndrome attenuates transition to severe obesity / Kodytková, Aneta (Rights reserved)
  • Laparoscopic adrenalectomy in children with diverse adrenal pathologies: the impact of pre-operative imaging in decision making process / Kravarusic, Dragan (Rights reserved)
  • Evaluation of continuous glucose monitoring and nutritional status in glycogen storage diseases / Kumru Akin, Burcu (Rights reserved)
  • ˜Theœ impact of the COVID-19 pandemic on DKA severity in Black and White pediatric patients / Patel, Shrina (Rights reserved)
  • ˜Theœ effect of phlebotomy and placement of an intravenous catheter on plasma catecholamine and serum copeptin concentrations / Sastry, Shruti (CC BY)
  • Clinical and genetic diagnosis of first cohort of differences of sexual development in the Iranian population / Rastari, Mandana (Rights reserved)
  • Nephrogenic diabetes insipidus results from a novel in-frame deletion of AVPR2 gene in monozygotic-twin boys and their mother and grandmother / Qin, Shengfang (CC BY)
  • Autosomally dominantly inherited isolated gonadotropin deficiency via maternal assisted reproduction due to SOX10 mutation / Bakjaji, Shadi (Rights reserved)
  • Causal associations between childhood obesity and delayed puberty or height: a bidirectional two-sample Mendelian randomization study / Cui, Lulu (CC BY)
  • Diabetes distress, depression, and future glycemic control among adolescents with type 1 diabetes / Damilano, Cecilia P. (Rights reserved)
  • Frontmatter (Rights reserved)
  • Development of bone mineral density and content in children with cerebral palsy: a retrospective, longitudinal study / Koebke, Philipp (Rights reserved)
  • Adrenal hypoandrogenism in adolescents with premature ovarian insufficiency / Bilici, Meliha Esra (Rights reserved)
  • Clinical manifestations and molecular genetics of seven patients with Niemann–Pick type-C: a case series with a novel variant / Kara, Cemre (CC BY)
  • Determinants of childhood and adolescent obesity and it’s effect on metabolism in South Indian population / Palanivel, Sengottaiyan (Rights reserved)
  • Effect of empagliflozin treatment on laboratory and clinical findings of patients with glycogen storage disease type Ib: first study from Türkiye / Köse, Engin (CC BY)
  • Dramatic response to Evinacumab in a North Indian girl with homozygous familial hypercholesterolemia / Arora, Sonali (Rights reserved)
  • Assessing the efficacy of a hybrid closed loop system in a racial-ethnic minority cohort of children and adolescents with type 1 diabetes / Granados, Andrea (Rights reserved)
  • Unclear symptoms, early diagnosis and perfect outcome: a case diagnosed as sepiapterin reductase deficiency hidden behind vitamin B12 deficiency / Akbeyaz, İsmail Hakkı (Rights reserved)
  • Cardiac function in children with congenital adrenal hyperplasia / Çetin, Tuğba Kontbay (Rights reserved)
  • Age and sex mark clinical differences in the presentation of pediatric type 1 diabetes mellitus / Gupta, Esha A. (Rights reserved)
  • Clinical and genetic insights into congenital lipoid adrenal hyperplasia: a case series from a tertiary care center in North India / George, Arun (Rights reserved)
  • Emergence of osteolysis as a new radiological feature in a case with a novel BMP2 gene variant / Süncak, Suzan (Rights reserved)
  • High yield of congenital hypothyroidism among infants attending Children Hospital, Nairobi, Kenya. Facility based study in the absence of newborn screening / Kahssay, Menbere (CC BY)
  • Optimal vitamin D status for Chinese infants in Hong Kong: insights from the relationship between serum 25-hydroxyvitamin D and parathyroid hormone levels / Tung, Joanna Yuet-Ling (Rights reserved)
  • Coexistence of SRY, DHX37 and POR gene variants in a patient with 46,XY disorder of sex development / Ozden, Ayse (Rights reserved)
  • Acrodermatitis dysmetabolica: lessons from two pediatric cases / Kahraman, Ayça Burcu (Rights reserved)
  • Frontmatter (Rights reserved)
  • Frontmatter (Rights reserved)
  • Diagnostic value of fasting insulin and insulin-like growth factor-1 levels in girls with central precocious puberty / Zhang, Hong-ru (Rights reserved)
  • Presence of hyperandrogenemia in cases evaluated due to menstrual irregularity, the effect of clinical and/or biochemical hyperandrogenemia on polycystic ovary syndrome / Koca, Serkan Bilge (Rights reserved)
  • CRH receptor antagonist crinecerfont – a promising new treatment option for patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency / Kamrath, Clemens (CC BY)
  • Frontmatter (Rights reserved)
  • Frontmatter (Rights reserved)
  • Moebius syndrome and hypopituitarism: a case of multiple pituitary hormone deficiency and revision of the literature / Molinari, Silvia (Rights reserved)
  • Evinacumab as an adjunct to lipid apheresis in an infant with homozygous familial hypercholesterolemia / Stirnkorb, Christian (CC BY)
  • ˜Theœ causal role of endocrine disrupting chemicals in pubertal timing: a Mendelian randomization study / Zuo, Melody (CC BY)
  • Diagnostic challenges in pediatric Cushing’s disease associated with chronic renal failure: a report of three patients / Martínez Castillo, Iratxe (Rights reserved)
  • Is oxytocin related to psychiatric symptoms in adolescents with obesity? / Özyurt, Gonca (Rights reserved)
  • Optimal timing of repeat thyroid fine-needle aspiration biopsy / Cay, Mevra (Rights reserved)
  • Assessment of quality of life in families affected by maple syrup urine disease: a cross sectional study / Magdy, Rofaida M. (Rights reserved)
  • Effects of orlistat on body mass index and serum lipids in overweight and obese adolescents: a meta-analysis / Zhang, Lingnan (Rights reserved)
  • Hormonal therapy for impaired growth due to pediatric-onset inflammatory bowel disease: a systematic review and meta-analysis with trial sequential analysis / Melo, Mardhen Catunda Rocha (Rights reserved)
  • Two families, two pathways: a case series of 46, XY DSD with 17α-hydroxylase deficiency and isolated 17,20-lyase deficiency due to novel CYB5A variant / Garg, Rakesh (Rights reserved)
  • Sunlight, supplements, and science: vitamin D as a tool for pediatric health care / Kamrath, Clemens (Rights reserved)
  • Associations between body mass index and sleep duration in Brazilian children and adolescents: the moderating role of screen time / Borfe, Leticia (Rights reserved)
  • Differentiating true precocious puberty and puberty variants in consecutive 275 girls: a single center experience / Sarıkaya, Emre (Rights reserved)
  • Persistent hypoglycemia in congenital syphilis: hyperinsulinemic hypoglycemia with a focal pancreatic lesion / Akyar, Mehmet (Rights reserved)
  • Endocrinopathies in children with inborn errors of immunity: a single-center experience / Buyukyilmaz, Gonul (Rights reserved)
  • Newborn screening follow-up in Bavaria: height and weight in paediatric patients with congenital adrenal hyperplasia / Dubinski, Ilja (Rights reserved)
  • Coexistence of phenylketonuria and tyrosinemia type 3: challenges in the dietary management / Selamioğlu, Arzu (Rights reserved)
  • Central precocious puberty in a toddler with hypothalamic hamartoma / Turhan, Banu (Rights reserved)
  • Neonatal hypoglycaemia in the offsprings of parents with maturity-onset diabetes of the young (MODY) / Maly, Jakub (Rights reserved)
  • Short- to medium-term follow-up of normoponderal children and adolescents with subclinical hypothyroidism: a retrospective study of the last 15 years / Moreira Esteves, Inês (Rights reserved)
  • A recent update on childhood obesity: aetiology, treatment and complications / Hawton, Katherine (Rights reserved)
  • Effect of a GnRH injection on kisspeptin levels in girls with suspected precocious puberty: a randomized-controlled pilot study / Rodanaki, Maria (CC BY)
  • Retrospective assessment of hepatic involvement in patients with inherited metabolic disorders: nine-year single-center experience / Bayramova, Samira (CC BY)
  • Clinical outcomes of switching to lonapegsomatropin from somatropin for treatment of pediatric growth hormone deficiency / Coyne, Emma (Rights reserved)
  • Vitamin D dependent rickets type 2A: a case series of two siblings with novel mutation in vitamin D receptor gene responded to high dose oral calcium and calcitriol / Mehak, Noor-ul-ain (Rights reserved)
  • Chronotype, sleep, and glycemic control in children and adolescents with type 1 diabetes: a case-control study / Can Yilmaz, Gulay (Rights reserved)
  • Neonatal severe hyperparathyroidism with inactivating calcium sensing receptor (CaSR) mutation (p.I81K) / Donbaloglu, Zeynep (Rights reserved)
  • Impact of growth hormone therapy on bone and body composition in prepubertal children with idiopathic short stature / Cho, Min Hyung (CC BY)
  • Bioinformatics analysis explores key pathways and hub genes in central precocious puberty / Guo, Na (Rights reserved)
  • Interpreting positive celiac serology in children with new-onset type 1 diabetes / Ramharack, Lydia (CC BY)
  • Diabetes, macrocytosis, and skin changes in large-scale mtDNA deletion / Krnic, Nevena (Rights reserved)
  • Frontmatter (Rights reserved)
  • Clinical and laboratory characteristics of propionic acidemia in a Turkish cohort / Akar, Halil Tuna (Rights reserved)
  • Prader-Willi syndrome gene expression profiling of obese and non-obese patients reveals transcriptional changes in CLEC4D and ANXA3 / Yoon, Ju Young (Rights reserved)
  • Patterns and determinants of serum amylase, lipase concentrations in Indian adolescents and youth with type 1 diabetes / Dange, Nimisha Shankar (CC BY)
  • Relationship between blood lipids and bone mineral density in healthy preschoolers: a 12-month cohort study / Mao, Xueqian (Rights reserved)
  • Pubertal disorders in juvenile idiopathic arthritis: a systemic review / Boussaid, Soumaya (Rights reserved)
  • Expanding the genotypic spectrum of 3β-hydroxy-δ5-C27-steroid dehydrogenase (HSD3B7) deficiency: novel mutations and clinical outcomes / Yoldaş Çelik, Merve (Rights reserved)
  • A systematic review and meta-analysis of the self-reported Pubertal Development Scale’s applicability to children / Pan, Dongxue (Rights reserved)
  • Differentiated thyroid cancer in adolescents – does extent of disease at presentation differ with age? / Arya, Priya (Rights reserved)
  • Insights in non-CAH pediatric primary adrenal insufficiency: a single-center experience from India / Daga, Aaditya (Rights reserved)
  • Psychological and behavioral assessments in girls with idiopathic central precocious puberty / Uthayo, Warisa (Rights reserved)
  • Rare case of ACTH-independent Cushing syndrome: diagnostic challenges and management / Salazar, Luís (Rights reserved)
  • Pediatric Graves’ disease in Argentina: analyzing treatment strategies and outcomes / Rothenfusser, Anna (Rights reserved)
  • Assessing prediabetes and cardiometabolic risk in Danish youth with obesity / Gaul, Anna Katrine (Rights reserved)
  • Infant gonadotropins predict spontaneous puberty in girls with Turner syndrome / Sawyer, Alexandra (Rights reserved)
  • Do children with type 1 diabetes mellitus remain protected against hepatitis B? / Yılmazbaş, Pınar (Rights reserved)
  • Geographic information system mapping and predictors of glycemic control in children and youth with type 1 diabetes: a study from Western India / Yewale, Sushil (CC BY)
  • Cord blood metabolomic profiling in high risk newborns born to diabetic, obese, and overweight mothers: preliminary report / Ünal Uzun, Özlem (Rights reserved)
  • DNA ligase IV deficiency identified in a patient with hypergonadotropic hypogonadism: a case report / Yasar, Deniz (Rights reserved)
  • ˜Theœ clinical characteristics of 10 cases and adult height of six cases of rare familial male-limited precocious puberty / Xie, Dandan (CC BY)
  • Elastographic evaluation for fatty liver disease in north Indian children and adolescents with type 1 diabetes / Gupta, Vinod (Rights reserved)
  • Outcomes of newborns screened for congenital hypothyroidism in Turkey – a single center experience / Esen, Ihsan (Rights reserved)
  • Development of a disease diagnostic model to predict the occurrence of central precocious puberty of female / Zhao, Manman (CC BY)
  • A novel de novo missense OTC mutation in an Iranian girl: a case report / Bahadoran, Ensiyeh (Rights reserved)
  • ˜Theœ effect of antenatal steroids on metabolic bone disease of prematurity / Erol, Sara (Rights reserved)
  • Medium-chain acyl-CoA dehydrogenase deficiency in North Macedonia – ten years experience / Anastasovska, Violeta (Rights reserved)
  • Immune checkpoint inhibitors and endocrinopathies in pediatric brain tumor patients / Westermann, Carly R. (CC BY)
  • Osteogenesis imperfecta: shifting paradigms in pathophysiology and care in children / Stasek, Stefanie (CC BY)
  • Impact of Covid-19 on children and adolescents with type 1 diabetes: lifestyle, telecommunication service, and quality of life / Matter, Randa M. (Rights reserved)
  • ˜Theœ transfer of care experience in young adults with type 1 diabetes / Yerges, April (Rights reserved)
  • Validity and reliability of parent assessments of pubertal maturation among adolescent girls in Isfahan, Iran / Mozafarian, Nafiseh (Rights reserved)
  • Dihydropyrimidinase deficiency with atrioventricular septal defect: a case report / Erdal, İzzet (Rights reserved)
  • Glucose and lipid-related indicators in relation to elevated alanine aminotransferase in a pediatric population / Momeni, Azin (Rights reserved)
  • Diabetic ketoacidosis in youth with diabetes mellitus during the COVID-19 pandemic / Cymbaluk, Anna (Rights reserved)
  • Author’s reply “Comment on diagnostic utility of the average peak LH levels measured during GnRH stimulation test” / Koca, Serkan Bilge (Rights reserved)
  • Frontmatter (Rights reserved)
  • Post hoc subgroup analysis of Asian children with paediatric GHD from the global phase 3 efficacy and safety study of once-weekly somatrogon vs. once-daily somatropin / Gomez, Roy (CC BY)
  • Refractory hypothyroidism in children: an overview / Metwalley, Kotb Abbass (Rights reserved)
  • Frontmatter (Rights reserved)
  • Relationship between urinary sodium excretion and bone mineral density in pediatrics: population-based study from KNHANES V 2010–2011 / Lee, In Kyung (Rights reserved)
  • Factors associated with neonatal hyperinsulinemic hypoglycemia, a case-control study / Rattanasakol, Thanaporn (Rights reserved)
  • Pronounced neonatal breast enlargement beyond the first week of life and its regression correlates with serum prolactin levels – a case series / Bartos, Hilda-Brigitta (Rights reserved)
  • Comment on “Diagnostic utility of the average peak LH levels measured during GnRH stimulation test” / Daungsupawong, Hinpetch (Rights reserved)
  • Diagnosis and approach of pseudohypoparathyroidism type 1A and related disorders during long term follow-up: a case report / Expósito Raspeño, Mónica (Rights reserved)
  • Controlled attenuation parameter (CAP): the clinical value based on MRI-PDFF in children with obesity / Peng, Tianfang (CC BY)
  • Exploring ketoacidosis frequency and risk factors in childhood-onset type 1 diabetes: an 8-year retrospective study (2011–2018) at a tertiary paediatric hospital in Tripoli, Libya / Shebani, Mostafa Sasi (Rights reserved)
  • Long-term effectiveness and safety of long-acting growth hormone preparation in children with growth hormone deficiency / Kang, Eungu (CC BY)
  • Association of hepatokines with markers of endothelial dysfunction and vascular reactivity in obese adolescents / Stein, David (Rights reserved)
  • Premature ovarian insufficiency in pediatric cancer patients: a 10 year Rady Children’s Hospital experience / Robinson, Miranda (Rights reserved)
  • Investigating the connection among thyroid function, sensitivity to thyroid hormones, and metabolic syndrome in euthyroid children and adolescents affected by type 1 diabetes / Calcaterra, Valeria (Rights reserved)
  • ˜Theœ effect of GnRH analog treatment on BMI in children treated for precocious puberty: a systematic review and meta-analysis / Zhu, Xiaoxiao (Rights reserved)
  • Does an episode of diabetic ketoacidosis affect thyroid function tests in pediatric patients? / Atakul, Gülhan (Rights reserved)
  • Treatment modalities and outcomes in pediatric Cushing’s disease – report of three cases and literature review / Marques, Viviana (Rights reserved)
  • ˜Theœ effect of gonadotropin-releasing hormone analog treatment on the endocrine system in central precocious puberty patients: a meta-analysis / Guo, Na (Rights reserved)
  • Novel PIK3R1 gene mutation associated with SHORT syndrome: a case report of a 15-year-old female / Osman, Amani (Rights reserved)
  • Presence of metabolic syndrome markers in very low birth weight ex-premature infants during early adolescence / Dinerstein, Alejandro (Rights reserved)
  • Adult endocrinologists’ perspectives on transitioning adolescent patients with congenital adrenal hyperplasia / Hall, Mary-Frances E. (Rights reserved)
  • Ovarian hyperthecosis in adolescent females: two case reports and a review of the literature / Angley, Eleanor (Rights reserved)
  • Diabetes and CFAP126 gene mutation; are they really linked together? / Arshad, Kashan (Rights reserved)
  • New data supporting that early diagnosis and treatment are possible and necessary in intracellular cobalamin depletion: the case of transcobalamin II deficiency / Bindi, Verónica (Rights reserved)
  • Frontmatter (Rights reserved)
  • Incidences of newly diagnosed childhood diabetes and onset severity: a multicenter regional study in Thailand over two decades and during the COVID-19 pandemic / Sinthuprasith, Pattharaporn (Rights reserved)
  • Timing of onset of menses after GnRH agonist treatment for central precocious puberty / Klein, Karen O. (Rights reserved)
  • Robust growth hormone responses to GH-releasing peptide 2 in adolescents / Onuki, Takanori (Rights reserved)
  • Early juvenile cataract in newly diagnosed type 1 diabetic patients: a description of two cases / Wu, Shimin (Rights reserved)
  • Growth pattern, growth deceleration, and relevant predictors in girls treated with GnRHa: a retrospective longitudinal study / Ouyang, Lixue (CC BY)
  • Growth hormone treatment in children with short stature: impact of the diagnosis on parents / Witt, Stefanie (Rights reserved)
  • A pilot study proposing an algorithm for pubertal induction in cerebral palsy / Trinh, Anne (CC BY)
  • Retrospective evaluation of patients diagnosed with central precocious puberty who reached the final height / Yaman, Kadri (Rights reserved)
  • Selecting optimal progestational agents either alone or in combination in common pediatric endocrine settings: challenges of unmet needs / Reich, Jenna (CC BY)
  • Decline in case rates of youth onset type 2 diabetes in year three of the COVID-19 pandemic / Kim, Ahlee (CC BY)
  • A new onset drug induced diabetes mellitus presenting with diabetic ketoacidosis in a child undergoing treatment for B cell acute lymphoblastic leukemia. A case report and review of literature / Sharma, Preeti (Rights reserved)
  • Ectopic lingual thyroid with subclinical hypothyroidism in children / An, Se Jin (Rights reserved)
  • From neglect to peril: diabetic ketoacidosis unleashing colonic necrosis and perforation in an adolescent girl with type 1 diabetes mellitus / Kumar, Mritunjay (Rights reserved)
  • New Editor-in-Chief of the Journal of Pediatric Endocrinology and Metabolism / Kiess, Wieland (Rights reserved)
  • Association between perinatal and obstetric factors and early age at diagnosis of type 1 diabetes mellitus: a cohort study / Negrato, Carlos A. (Rights reserved)
  • STX16 exon 5–7 deletion in a patient with pseudohypoparathyroidism type 1B / Chen, Li (Rights reserved)
  • Predictive factors for lung metastasis in pediatric differentiated thyroid cancer: a clinical prediction study / Kuang, Hou-fang (Rights reserved)
  • Use of (18 F) fluorocholine PET/CT in the detection of primary hyperparathyroidism in paediatrics: a case report / Martínez Sánchez, Helena (Rights reserved)
  • Frontmatter (Rights reserved)
  • Mental disorders in children and adolescents with type 1 diabetes before and during the COVID-19 pandemic: results from the DPV registry / Müller-Godeffroy, Esther (Rights reserved)
  • Long term clinical follow up of four patients with Wolfram syndrome and urodynamic abnormalities / Dange, Nimisha S. (Rights reserved)
  • Evaluation of the role of FTO (rs9939609) and MC4R (rs17782313) gene polymorphisms in type 1 diabetes and their relation to obesity / Mosaad, Youssef M. (Rights reserved)
  • Homozygous mutation of KISS1 receptor (KISS1R) gene identified in a Chinese patient with congenital hypogonadotropic hypogonadism (CHH): case report and literature review / Chen, Xiaoqian (Rights reserved)
  • Variable presentation and outcomes of primary hyperparathyroidism in children and adolescents / Das, Debaditya (Rights reserved)
  • Urinary biomarkers NG AL and beta-2 microglobulin in children with type 1 diabetes mellitus / Sachan, Nimisha (Rights reserved)
  • Diagnostic utility of the average peak LH levels measured during GnRH stimulation test / Koca, Serkan Bilge (Rights reserved)
  • Insulin for “hearts that had lost hope” – on the first pediatric patients and the 1923 Nobel Prize in Physiology or Medicine / Popescu, Iuliana (Rights reserved)
  • Diurnal 11-ketotestosterone and 17-hydroxyprogesterone saliva profiles in paediatric classical congenital adrenal hyperplasia / Dubinski, Ilja (Rights reserved)
  • Growth hormone therapy does not impact the development of intracranial hypertension in children with Chiari malformation / Krasnow, Matthew D. (Rights reserved)
  • Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta / Evin, Ferda (Rights reserved)
  • An infant developing hypercalcemia and hypophosphatemia due to the use of exclusively almond milk / Salama, Mostafa (Rights reserved)
  • A case report of odonto-hypophosphatasia with a novel variant in the ALPL gene / Oto, Yuji (Rights reserved)
  • Computed tomography–guided percutaneous cryoablation of hereditary adrenal pheochromocytoma in three patients / Griffing, Emily (Rights reserved)
  • Endocrinological and metabolic profile of Gaucher disease patients treated with enzyme replacement therapy / Kilic, Ayse (Rights reserved)
  • Reliability of self-reported pubertal development scale for girls in early adolescent: a school population-based study / Lin, Cuilan (Rights reserved)
  • Hypothyroxinemia and weight velocity in preterm infants / Zibitt, Meira (Rights reserved)
  • Estrogen-insensitivity syndrome (EIS) in a female adolescent patient – a case report / Soltani, Akbar (Rights reserved)
  • A 14-year-old girl with premature ovarian insufficiency but with a positive pregnancy test / Touwslager, Robbert N.H. (CC BY)
  • Congenital hyperinsulinism patient with ABCC8 and KCNJ11 double heterozygous variants: a case report with 6 years follow-up / Hui, Peipei (Rights reserved)
  • Comprehensive analyses of phenylalanine hydroxylase variants and phenotypic characteristics of patients in the eastern region of Türkiye / Alavanda, Ceren (Rights reserved)
  • Allergic reactions to enzyme replacement therapy in children with lysosomal storage diseases and their management / Arik, Elif (Rights reserved)
  • Benign transient hyperphosphatasemia in the pediatric population: a single center cohort study / Buyukyilmaz, Gonul (Rights reserved)
  • Outcomes of growth hormone treatment in children with Prader–Willi syndrome over a 30-year period: a single tertiary center experience / Gamage, Dilhara S. (CC BY)
  • Evaluation of aortic elasticity properties in mucopolysaccharidosis patients; effect of enzyme replacement therapy (ERT) on aortic stiffness / Ertas, Kerem (Rights reserved)
  • Surgical treatment of secondary hyperparathyroidism in children with chronic kidney disease. Experience in 19 patients / Gil, Silvia Mercedes (Rights reserved)
  • ˜Theœ effect of phenylketonuria on family quality of life / Iakovou, Kostas Konstantinos (Rights reserved)
  • Another look at the necessity of polysomnography for infants with Prader-Willi syndrome prior to initiation of growth hormone therapy / Ismail, Esraa (Rights reserved)
  • Long-term efficacy and safety of PEGylated recombinant human growth hormone in treating Chinese children with growth hormone deficiency: a 5-year retrospective study / Hou, Lele (Rights reserved)
  • Growth after pediatric kidney transplantation: a 25-year study in a pediatric kidney transplant center / Claro, Ana Raquel (Rights reserved)
  • New data supporting that early diagnosis and treatment are possible and necessary in intracellular cobalamin depletion: the case of transcobalamin II deficiency / Verónica, Bindi (Rights reserved)
  • A novel useful marker in the early discrimination of transient hyperthyrotropinemia/hypothyroxinemia and congenital hypothyroidism in preterm infants: thyroid-stimulating hormone/free thyroxine ratio / Cakir, Ufuk (Rights reserved)
  • Thyroid hormone resistance and large goiter mimicking infiltrative carcinoma in a pediatric patient / Baxter, Carly (Rights reserved)
  • Ovarian reserve and fertility parameters in post-pubertal females with congenital adrenal hyperplasia: a case-control study / Nawar, Marwa (Rights reserved)
  • Through the eyes of the parents: a transdiagnostic psychiatric perspective for children with differences of sexual development / Ozbaran, Burcu (Rights reserved)
  • Slow growth and short stature in children with attention deficit hyperactivity disorder (ADHD): a retrospective study of 493 children who underwent growth hormone provocation testing at one tertiary paediatric endocrine centre / Velayutham, Vallimayil (Rights reserved)
  • Examination of quality of life and psychiatric symptoms in childhood Graves’ disease / Yazkan Akgül, Gözde (Rights reserved)
  • Effect and safety of aromatase inhibitors for the treatment of short stature in male children and adolescents: a meta-analysis of randomized controlled trials / Ye, Ruxia (Rights reserved)
  • Struggle for the future health of adolescent patients with phenylketonuria and parents with a sick child due to the economic crisis / Iakovou, Kostas (Rights reserved)
  • Expanded phenotypic spectrum in MODY 5 patients with 17q12 deletion syndrome: experience from an Indian tertiary care hospital / Misgar, Raiz A. (Rights reserved)
  • A very rare presentation of mitochondrial elongation factor Tu deficiency- TUFM mutation and literature review / Gokalp, Sabire (Rights reserved)
  • A rare case of central precocious puberty in a male infant with adrenal hypoplasia congenita / Mastoropoulou, Aikaterini (Rights reserved)
  • Automated insulin delivery in children with type 1 diabetes during physical activity: a meta-analysis / Wang, Yuan-yuan (Rights reserved)
  • Effect of daily zinc supplementation for 12 weeks on serum thyroid auto-antibody levels in children and adolescents with autoimmune thyroiditis – a randomized controlled trial / Sivakumar, Ramachandran (Ramge) (Rights reserved)
  • ˜Theœ role of Cardiotrophin-1 and echocardiography in early detection of subclinical diabetic cardiomyopathy in children and adolescents with type 1 diabetes mellitus / Hassanein, Samah A. (Rights reserved)
  • Hsa_circ_0002473 inhibits GH3 cell proliferation and GH secretion as a competitive endogenous RNA for has-miR-4645-3p / Pan, Kaiyu (Rights reserved)
  • ˜Theœ relationship between bisphenol A and phthalates with precocious puberty in Vietnamese children / Vu Huynh, Quynh Thi (Rights reserved)
  • Thyroid abscess associated with transient hyperthyroidism in an adolescent girl: a rare case report and review of the literature / Gaur, Bablu K. (Rights reserved)
  • Frontmatter (Rights reserved)
  • Medulloblastoma in a child with osteoma cutis – a rare association due to loss of GNAS expression / Suntharesan, Jananie (Rights reserved)
  • Thyroid volume in Turkish school-age children living in an iodine-sufficient region / Deveci Sevim, Reyhan (Rights reserved)
  • Evaluation of the etiology of subclinical hypothyroidism in children / Yaşar, Ayşe (Rights reserved)
  • A rare case of skeletal dysplasia: biallelic variant in ACAN gene / Arslan, Gülçin (Rights reserved)
  • Tackling access and payer barriers for growth hormone therapy in Saudi Arabia: a consensus statement for the Saudi Working Group for Pediatric Endocrinology / Attia, Najya (CC BY)
  • Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in GRN gene: case report and review of literature / Sürücü Kara, İlknur (Rights reserved)
  • Newborn screening for primary carnitine deficiency using a second-tier genetic test / Lin, Yiming (Rights reserved)
  • ˜Theœ complexities of managing a newborn with 6q24 transient neonatal diabetes mellitus: a case report / De Silva, Yannick (Rights reserved)
  • Reviewer Acknowledgment (Rights reserved)
  • New perspectives for the treatment and follow-up of glycogen storage disease type V: DL-3-hydroxybutyric acid with modified Atkins diet and quadriceps femoris shear wave elastography / Özsaydı Aktaşoğlu, Ekin (Rights reserved)
  • Artificial intelligence in paediatric endocrinology: conflict or cooperation / Dimitri, Paul (Rights reserved)
  • Gly183Ser homozygous mutation of the steroid 5-a reductase type 2 (SRD5A2) gene in a Brazilian patient: case report / Laureano, Daniela P. (Rights reserved)
  • Evaluation of cardiac electrophysiological features in patients with premature adrenarche / Ertaş, Kerem (Rights reserved)
  • Pituitary stalk interruption syndrome due to novel ROBO1 mutation presenting as combined pituitary hormone deficiency and central diabetes insipidus / Misgar, Raiz Ahmad (Rights reserved)
  • Evaluation of the systemic-immune inflammation index (SII) and systemic immune-inflammation response index (SIRI) in children with type 1 diabetes mellitus and its relationship with cumulative glycemic exposure / Ozde, Sukriye (Rights reserved)
  • Association between proinflammatory cytokines and arterial stiffness in type 1 diabetic adolescents / Reis, Mónica (Rights reserved)
  • Frontmatter (Rights reserved)
  • Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review / Sonuç Kartal, Gülreyhan (Rights reserved)
  • Hereditary spastic paraplegia type 35 in a Turkish girl with fatty acid hydroxylase-associated neurodegeneration / Engin Erdal, Ayşenur (Rights reserved)
  • Association between maternal and cord blood thyroid hormones, and urine iodine concentration with fetal growth / Alimardani, Bita (Rights reserved)
  • Do body esteem and quality of life scores change with puberty signs or precocious puberty treatment? / Koca, Serkan Bilge (Rights reserved)
  • Mineralocorticoid receptor antagonist monotherapy in pediatric non-classical 11β-hydroxylase deficiency / Kennedy, Elaine C. (Rights reserved)
  • Children and adolescents with differentiated thyroid cancer from 1998 to 2018: a retrospective analysis / Li, Wei (Rights reserved)
  • Review on the screening of urine glucose for early diagnosis of type 2 diabetes mellitus in school children and adolescents with obesity in Hong Kong / Pang, Gloria Shir-Wey (Rights reserved)
  • Lymphedema in Turner syndrome: correlations with phenotype and karyotype / Ikomi, Chijioke (Rights reserved)
  • Comparison of the effectiveness of prepubertal growth hormone treatment on height and predicted adult height in children with short stature born small for gestational age vs. with a growth hormone deficiency / Tanaka, Toshiaki (Rights reserved)
  • Experiences and psychological issues affecting parents of children born with atypical genitalia in India / Bindal, Tanvi (Rights reserved)
  • A successful liver transplantation in a patient with neonatal-onset carbamoyl phosphate synthetase-1 deficiency / Arslan, Sezai (Rights reserved)
  • Selpercatinib prior to radioactive iodine for pediatric papillary thyroid carcinoma / Chiu, Harvey K. (Rights reserved)
  • Early blood glucose screening in asymptomatic high-risk neonates / El-Khawam, Rania (CC BY)
  • Trajectory of the body mass index of children and adolescents attending a reference mental health center / Echeveste-Navarrete, Juliana (Rights reserved)
  • Timing of onset of menses after GnRH agonist treatment for central precocious puberty / Klein, Karen O. (Rights reserved)
  • Do hybrid closed loop insulin pump systems improve glycemic control and reduce hospitalizations in poorly controlled type 1 diabetes? / Farhat, Ilham (Rights reserved)
  • Frontmatter (Rights reserved)
  • Prenatal presentation of a hyperfunctioning thyroid nodule / Scrushy, Marinda G. (Rights reserved)
  • Lack of association between month of birth and risk of developing type 1 diabetes in Brazil: a 40-year analysis / Lanzarin, João Vitor Mota (Rights reserved)
  • Frontmatter (Rights reserved)
  • Implementation of the Mind Youth Questionnaire (MY-Q) for routine health-related quality of life screening of adolescents with type 1 diabetes in a large tertiary care center / Stojanova, Aleksandra (Rights reserved)
  • Oral glucose tolerance test curve shape in Mexican children and adolescents with and without obesity / Evia-Viscarra, María Lola (Rights reserved)
  • Gonadal changes in children and adolescents with congenital adrenal hyperplasia / Mahmoud, Rana (Rights reserved)
  • Familial dysalbuminemic hyperthyroxinemia (FDH) due to Arg242 His variant in ALB gene in Turkish children / Turkkahraman, Doga (Rights reserved)
  • Applicability of the External Genitalia Score (EGS) in Indian neonates and children up to 2 years of age / Nanda, Pamali Mahasweta (Rights reserved)
  • Alterations in optical coherence tomography and optical coherence tomography angiography findings in children with partial biotinidase deficiency / Karataş, Gamze (Rights reserved)
  • Endocrine sequelae after pediatric craniopharyngioma treatment: a single-center retrospective cohort study / Papy, Marie (Rights reserved)
  • Early change of retinal nerve fiber layer in children with type 1 diabetes mellitus in northern China / Wu, Dejing (Rights reserved)
  • Identification of a novel homozygous NR5A1 variant in a patient with a 46,XY disorders of sex development / Kırkgöz, Tarık (Rights reserved)
  • SRY -positive 45,X/46,XY karyotype in a phenotypically Turner-like Chinese adolescent female with ovarian dysgerminoma and gonadoblastoma / Zhou, Jiahong (Rights reserved)
  • A novel variant of the STAR gene: nonclassical presentation from Turkey / Aytaç Kaplan, Emel Hatun (Rights reserved)
  • Incidence and associated risk factors of congenital hypothyroidism among newborns in Hainan, China: a retrospective study / Zhao, Zhendong (Rights reserved)
  • Late diagnosis of the X-linked MCT8 deficiency (Allan–Herndon–Dudley syndrome) in a teenage girl with primary ovarian insufficiency / Sriram, Swetha (Rights reserved)
  • Evaluation of copeptin in children after stimulation with clonidine or L-Dopa / Giannakopoulos, Aristeidis (Rights reserved)
  • Assessment of diabetes-specific knowledge and its determinants among children with type 1 diabetes mellitus and their primary caregivers: Experience from a tertiary care center in North India / Maheshwari, Rimjhim (Rights reserved)
  • Frontmatter (Rights reserved)
  • Frontmatter (Rights reserved)
  • Effective and safe use of sirolimus in hyperinsulinemic hypoglycaemia refractory to medical and surgical therapy: a case series and review of literature / Burnside, Mercedes J. (Rights reserved)
  • Novel homozygous mutation in SCNN1A gene in an Iranian boy with PHA1B / Saffari, Fatemeh (Rights reserved)
  • Frontmatter (Rights reserved)
  • Frontmatter (Rights reserved)

Downloads

Downloads

Full record

TOC

Image fragment

Link to the viewer page with highlighted frame Link to IIIF image fragment

Formats and links

Cite

Cite

The following citation links are available for the entire work or the page displayed:

Full record

Citation recommendation

Please check the citation before using it.

Contact

Have you found an error? Do you have any suggestions for making our service even better or any other questions about this page? Please write to us and we'll make sure we get back to you.

What color is the blue sky?:

I hereby confirm the use of my personal data within the context of the enquiry made.