Subclinical but significant? Updated review of pediatric hypothyroidism / Cooper, Felicia (Rights reserved)

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Periodical

Creator:: Berlin

Title:: Berlin in Zahlen : Taschenbuch / herausgegeben vom Statistischen Amt der Stadt Berlin

Other titles:: Kleines Berliner Taschenbuch; Kriegstaschenbuch

Publisher:: Statistisches Amt der Stadt Berlin

Publication:: Berlin: Selbstverl. 1947

Digitization:: Berlin: Zentral- und Landesbibliothek Berlin, 2017

Dates of Publication:: 1929-1945

Note:: 1929-1933 erschienen als Beilage zu: Statistisches Jahrbuch der Stadt Berlin

ZDB-ID:: 2900800-1

Succeeding Title:: Berlin in Zahlen [Ost]

Berlin:: B 8 Allgemeines: Statistik

DDC Group:: 310 Statistik

Collection:: General Regional Studies

Copyright:: Public Domain

Accessibility:: Free Access

Creator:: Berlin

Title:: Berlin in Zahlen : Taschenbuch / herausgegeben vom Statistischen Amt der Stadt Berlin

Other titles:: Kleines Berliner Taschenbuch; Kriegstaschenbuch

Publisher:: Statistisches Amt der Stadt Berlin

Publication:: Berlin: Selbstverl. 1947

Digitization:: Berlin: Zentral- und Landesbibliothek Berlin, 2017

Dates of Publication:: 1929-1945

Note:: 1929-1933 erschienen als Beilage zu: Statistisches Jahrbuch der Stadt Berlin

ZDB-ID:: 2900800-1

Succeeding Title:: Berlin in Zahlen [Ost]

Berlin:: B 8 Allgemeines: Statistik

DDC Group:: 310 Statistik

Collection:: General Regional Studies

Copyright:: Public Domain

Accessibility:: Free Access

Volume

Publication:: 1938

Language:: German

Digitization:: Berlin: Zentral- und Landesbibliothek Berlin, 2017

Berlin:: B 8 Allgemeines: Statistik

DDC Group:: 310 Statistik

URN:: urn:nbn:de:kobv:109-1-10385612

Location:: Zentral- und Landesbibliothek Berlin

Shelfmark:: B 8/1

Copyright:: Public Domain

Accessibility:: Free Access

Collection:: General Regional Studies

Publication:: 1938

Language:: German

Digitization:: Berlin: Zentral- und Landesbibliothek Berlin, 2017

Berlin:: B 8 Allgemeines: Statistik

DDC Group:: 310 Statistik

URN:: urn:nbn:de:kobv:109-1-10385612

Location:: Zentral- und Landesbibliothek Berlin

Shelfmark:: B 8/1

Copyright:: Public Domain

Accessibility:: Free Access

Collection:: General Regional Studies

Chapter

Title:: XVII. Finanzen und Steuern

Title:: XVII. Finanzen und Steuern

Contents

Table of contents

The journal of pediatric endocrinology and metabolism (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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The impact of the COVID-19 pandemic on DKA severity in Black and White pediatric patients / Patel, Shrina (Rights reserved)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)
The 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)

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