Journal of Pediatric Endocrinology & Metabolism

Papers
(The median citation count of Journal of Pediatric Endocrinology & Metabolism is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-04-01 to 2025-04-01.)
ArticleCitations
A case report of a young boy with low renin and high aldosterone levels induced by Liddle syndrome who was previously misdiagnosed with primary aldosteronism26
Effect of complete suppression of androstenedione on auxological development in prepubertal patients with classical congenital adrenal hyperplasia26
Diagnosis of adrenal insufficiency in children: a survey among pediatric endocrinologists in North America21
Treatment modalities and outcomes in pediatric Cushing’s disease – report of three cases and literature review17
Medium-chain acyl-CoA dehydrogenase deficiency in North Macedonia – ten years experience15
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 glycemi15
Acrodermatitis dysmetabolica: lessons from two pediatric cases15
Interpreting positive celiac serology in children with new-onset type 1 diabetes15
The effects of topical iodine containing antiseptics on thyroidal status and early neurodevelopment of preterm infants14
Clinical, pathological and molecular spectrum of patients with glycogen storage diseases in Pakistan14
Evaluation of bladder dysfunction in children and adolescents with type 1 diabetes mellitus by uroflowmetry14
Thyroid abscess associated with transient hyperthyroidism in an adolescent girl: a rare case report and review of the literature13
Diagnostic utility of the average peak LH levels measured during GnRH stimulation test13
Evaluation of endocrinological involvement and metabolic status in patients with Gaucher disease Type 1 and Fabry disease under enzyme replacement therapy13
Approach to nutritional rickets12
Nephrogenic diabetes insipidus results from a novel in-frame deletion of AVPR2 gene in monozygotic-twin boys and their mother and grandmother12
Hypoparathyroidism and medium-chain Acyl-CoA dehydrogenase deficiency, an unusual association12
Frontmatter12
Accelerated pubertal onset in short children with delayed bone age12
Laparoscopic adrenalectomy in children with diverse adrenal pathologies: the impact of pre-operative imaging in decision making process11
Questioning the adequacy of standardized vitamin D supplementation protocol in very low birth weight infants: a prospective cohort study11
Moebius syndrome and hypopituitarism: a case of multiple pituitary hormone deficiency and revision of the literature11
Successful treatment of hypercalcemia in a Chinese patient with a novel homozygous mutation in the CYP24A1 gene using zoledronic acid: a case report10
Body mass index evolution and ovarian function in adolescent girls who received GnRH agonist treatment for central precocious puberty or early and fast puberty10
Analysis of the CAG tract length in the Androgen Receptor gene in Mexican patients with nonsyndromic cryptorchidism10
Urinary phthalate concentrations are associated with total fat mass in Thai children10
Association of muscle mass and fat mass on low-density-lipoprotein cholesterol and triglyceride plasma concentration in children and adolescents10
Frontmatter10
Infection with SARS-CoV-2 may alter the half-life of desmopressin (DDAVP) in patients with central diabetes insipidus9
Insulin for “hearts that had lost hope” – on the first pediatric patients and the 1923 Nobel Prize in Physiology or Medicine9
Normal or elevated prolactin is a good indicator to show pituitary stalk interruption syndrome in patients with multiple pituitary hormone deficiency9
Pediatric adrenocortical tumors cohort characteristics and long-term follow-up at a single Argentinian tertiary center9
Ectopic parathyroid hormone as a rare aetiology of hypercalcemia with rhabdomyosarcoma: a new treatment strategy with zoledronic acid and Denosumab9
Hereditary spastic paraplegia type 35 in a Turkish girl with fatty acid hydroxylase-associated neurodegeneration9
Apparent diffusion coefficient (ADC) measurements and morphometric evaluation of the cranium in age-matched children with central precocious puberty9
Depression, anxiety, eating problems, and diabulimia risk in adolescents with type 1 diabetes: a case–control study9
Long-term experience with the use of a single histrelin implant beyond one year in patients with central precocious puberty9
Rickets in proximal renal tubular acidosis: a case series of six distinct etiologies9
Adjustment of octreotide dose given via insulin pump based on continuous glucose monitoring (CGM) in a child with congenital hyperinsulinism9
The relationship between metabolic syndrome criteria and pentraxin-3 levels in children8
Outcomes of growth hormone treatment in children with Prader–Willi syndrome over a 30-year period: a single tertiary center experience8
Combined diagnostic value of insulin-like growth factor-1, insulin-like growth factor binding protein-3, and baseline luteinizing hormone levels for central precocious puberty in girls8
An endocrine perspective on menstrual suppression for adolescents: achieving good suppression while optimizing bone health8
The prevalence of incidental finding of gynecomastia on thoracic computed tomography in the pediatric age group8
Stretched penile length at birth: a systematic review8
Retrospective evaluation of patients diagnosed with central precocious puberty who reached the final height8
Sexual precocity in the setting of parental use of a compounded testosterone cream: case report and review of the literature8
Association of hepatokines with markers of endothelial dysfunction and vascular reactivity in obese adolescents8
Frontmatter8
Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets8
What is the relationship between obesity and new circadian rhythm parameters in Turkish children and adolescents? A case-control study8
Artificial intelligence in paediatric endocrinology: conflict or cooperation8
Lack of association between month of birth and risk of developing type 1 diabetes in Brazil: a 40-year analysis7
Clinical, biochemical, and radiological follow-up results of children and adolescents with Hashimoto’s thyroiditis: a single-center experience7
Caregivers’ knowledge and medication adherence in children with thyroid disorders: an exploratory study7
Graves’ disease after COVID mRNA vaccination for the first time diagnosed in adolescence-case report. Cause and effect relationship or simple coincidence?7
The coincidence of two rare diseases with opposite metabolic phenotype: a child with congenital hyperinsulinism and Bloom syndrome7
Initial neutrophil/lymphocyte and lymphocyte/monocyte ratios can predict future insulin need in newly diagnosed type 1 diabetes mellitus7
Myoinositol or D-chiro-inositol for PCOS symptoms in adolescents: a narrative review7
Screening for hypophosphatasia: does biochemistry lead the way?7
Interdisiplinary and intraobserver reliability of the Greulich-Pyle method among Turkish children7
Genome analyses and androgen quantification for an infant with 5α-reductase type 2 deficiency7
Anthropometric, biochemical and hormonal profiles of the partially admixed pygmoid group in Rampasasa (Flores, Indonesia)6
Associations between body mass index and sleep duration in Brazilian children and adolescents: the moderating role of screen time6
Diabetic ketoacidosis masquerading behind alkalemia an undiagnosed or missed variant of diabetic ketoacidosis6
Pronounced neonatal breast enlargement beyond the first week of life and its regression correlates with serum prolactin levels – a case series6
Glycogen storage disease type XII; an ultra rare cause of hemolytic anemia and rhabdomyolysis: one new case report6
The utility of reverse phenotyping: a case of lysinuric protein intolerance presented with childhood osteoporosis6
Novel homozygous inactivating mutation in the luteinizing hormone receptor gene (LHCGR) associated with 46, XY DSD in a Moroccan family6
Influence of the SARS-CoV-2 pandemic on paediatric patients with type 1 diabetes mellitus after one year of follow-up6
Pseudohypoaldosteronism associated with hypertrophic cardiomyopathy, hypertension and thrombocytosis due to mutation in the ELAC2 gene: a case report6
ALG11-CDG: novel variant and review of the literature6
Study of the frequency and clinical features of maturity-onset diabetes in the young in the pediatric and adolescent diabetes population in Iran6
The usefulness of copeptin for the diagnosis of nephrogenic diabetes insipidus in infancy: a case report6
Pattern of presentation of paediatric endocrine disorders in a Nigerian tertiary institution: an 11-year survey6
Transient neonatal hyperinsulinism: early predictors of duration6
Exaggerated mini-puberty in a preterm girl: a case report and review of literature6
Selecting optimal progestational agents either alone or in combination in common pediatric endocrine settings: challenges of unmet needs5
Growth hormone treatment and bone mineral density in pediatric patients with Prader–Willi syndrome5
Long-term follow-up of transient neonatal diabetes mellitus due to a novel homozygous c.7734C>T (p.R228C) mutation in ZFP57 gene: relapse at prepubertal age5
Optimal vitamin D status for Chinese infants in Hong Kong: insights from the relationship between serum 25-hydroxyvitamin D and parathyroid hormone levels5
Premature adrenarche in Prader–Willi syndrome is associated with accelerated pre-pubertal growth and advanced bone age5
Three novel mutations of the BCKDHA, BCKDHB and DBT genes in Chinese children with maple syrup urine disease5
Evaluation of efficacy and safety of long-acting PEGylated recombinant human growth hormone (Jintrolong) for patients with growth hormone deficiency5
Spectrum of PAH gene mutations and genotype–phenotype correlation in patients with phenylalanine hydroxylase deficiency from Turkey5
Identification of a novel homozygous NR5A1 variant in a patient with a 46,XY disorders of sex development5
A novel de novo missense OTC mutation in an Iranian girl: a case report5
Long-term follow-up of alkaptonuria patients: single center experience5
Author’s reply “Comment on diagnostic utility of the average peak LH levels measured during GnRH stimulation test”5
Investigation of the relationship between serum sclerostin and dickkopf-1 protein levels with bone turnover in children and adolescents with type-1 diabetes mellitus5
Comparison of insulin sensitivity indices for detection of double diabetes in Indian adolescents with type 1 diabetes5
Bioinformatics analysis explores key pathways and hub genes in central precocious puberty5
Does an episode of diabetic ketoacidosis affect thyroid function tests in pediatric patients?5
Assessing the efficacy of a hybrid closed loop system in a racial-ethnic minority cohort of children and adolescents with type 1 diabetes5
Persistent hypoglycemia in congenital syphilis: hyperinsulinemic hypoglycemia with a focal pancreatic lesion5
Assessment of pubertal onset and disorders of puberty in Indian children and youth with type-1 diabetes5
The long-term growth, cost-effectiveness, and glycemic effects of growth hormone therapy on children born small for gestational age over 10 years: a retrospective cohort study5
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 p5
Impact of Obesity on Bone Metabolism in Children5
Determinants of childhood and adolescent obesity and it’s effect on metabolism in South Indian population5
Evaluation of clinical, endocrine and metabolic findings in obese children with and without hepatosteatosis5
Successful treatment of severe hypertriglyceridemia with icosapent ethyl in a case of congenital generalized lipodystrophy type 45
Long term clinical follow up of four patients with Wolfram syndrome and urodynamic abnormalities5
Niemann–Pick type C disease with a novel intronic mutation: three Turkish cases from the same family5
Diagnostic challenges in pediatric Cushing’s disease associated with chronic renal failure: a report of three patients5
A novel useful marker in the early discrimination of transient hyperthyrotropinemia/hypothyroxinemia and congenital hypothyroidism in preterm infants: thyroid-stimulating hormone/free thyroxine ratio5
Evaluation of the pathophysiological role of Fetuin A levels in adolescents with polycystic ovary syndrome5
Comparison of regular with NPH insulin vs. premix insulin in children and adolescents with type 1 diabetes in a resources-limited setting: a retrospective data analysis4
Diagnostic re-evaluation and predictors of congenital hypothyroidism with eutopic thyroid gland in Jiangxi, China4
An update of the mutation spectrum of phenylalanine hydroxylase (PAH) gene in the population of Turkey4
Cardiometabolic risk factors in children and adolescents from southern Brazil: comparison to international reference values4
Association between anthropometric measures and insulin resistance in Brazilian adolescents: data from the national study of cardiovascular risk factors in adolescents – ERICA4
Mental disorders in children and adolescents with type 1 diabetes before and during the COVID-19 pandemic: results from the DPV registry4
Liraglutide combined with intense lifestyle modification in the management of obesity in adolescents4
Management challenges of Rabson Mendenhall syndrome in a resource limited country: a case report4
Oral glucose tolerance response curve predicts disposition index but not other cardiometabolic risk factors in healthy adolescents4
Optimal timing of repeat thyroid fine-needle aspiration biopsy4
The genetic elucidation of monogenic obesity in the Arab world: a systematic review4
Investigation of androgen receptor gene CAG repeat length polymorphism in pubertal gynecomastia4
Evaluation of serum telomerase activity in normal-weight young girls with polycystic ovary syndrome and its relation to metabolic parameters4
Pubertal induction therapy in pediatric patients with Duchenne muscular dystrophy4
Extremely and very preterm children who were born appropriate for gestational age show no differences in cortisol concentrations or diurnal rhythms compared to full-term children4
Newborn screening for primary carnitine deficiency using a second-tier genetic test4
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 somatropin4
A rare and preventable aetiology of neurodevelopmental delay and epilepsy: familial glucocorticoid deficiency4
Through the eyes of the parents: a transdiagnostic psychiatric perspective for children with differences of sexual development4
Evaluation of continuous glucose monitoring and nutritional status in glycogen storage diseases4
An atypical presentation of a pathogenic STK11 gene variant in siblings not fulfilling the clinical diagnostic criteria for Peutz-Jeghers Syndrome4
Newborn screening and genetic variation of medium chain acyl-CoA dehydrogenase deficiency in the Chinese population4
The clinical variations and diagnostic challenges of deoxyguanosine kinase deficiency: a descriptive case series4
Effect of obesity and excessive body fat on glycaemic control in paediatric type 1 diabetes4
The concordance between ultrasonographic stage of breast and Tanner stage of breast for overweight and obese girls: a school population-based study4
Prevalence of nonalcoholic fatty liver disease increased with type 2 diabetes mellitus in overweight/obese youth with polycystic ovary syndrome4
Adiposity measures in screening for metabolic syndrome among Chinese children and adolescents4
The prevalence, immune profile, and clinical characteristics of children with celiac disease and type 1 diabetes mellitus in the state of Qatar4
Mineralocorticoid receptor antagonist monotherapy in pediatric non-classical 11β-hydroxylase deficiency4
Early-onset growth hormone treatment in Prader–Willi syndrome attenuates transition to severe obesity4
Congenital generalized lipodystrophy type 4 due to a novel PTRF/CAVIN1 pathogenic variant in a child: effects of metreleptin substitution3
Identification of a novel mutation in the PHKA2 gene in a child with liver cirrhosis3
Identification of a novel mutation in the ALDOB gene in hereditary fructose intolerance3
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 India3
Perceptions and use of complementary and alternative medicine in patients with precocious puberty3
Predictive value of 6 h postoperative parathyroid hormone level on permanent hypoparathyroidism in pediatric total thyroidectomy: a pilot study3
Case report: mitochondrial diabetes mellitus in a Chinese family due to m.3243A>G3
Use of letrozole to augment height outcome in pubertal boys: a retrospective chart review3
Evaluation of copeptin in children after stimulation with clonidine or L-Dopa3
A case-control study of early-stage radiological markers of endothelial dysfunction and cardiovascular findings in patients with osteogenesis imperfecta: genotype–phenotype correlations3
Development and validation of a mobile application for point of care evaluation of growth failure3
Safety and user experience with off-label use of a flash glucose monitor (FreeStyle Libre® 1) among very young children with type 1 diabetes mellitus3
Serum spexin levels are not associated with size at birth but are associated with metabolic syndrome components in prepubertal children born at term3
Frontmatter3
Two Japanese siblings with arginase-1 deficiency identified using a novel frameshift mutation of ARG1 (p.Lys41Thrfs2)3
Medullary thyroid carcinoma in children: current state of the art and future perspectives3
Early juvenile cataract in newly diagnosed type 1 diabetic patients: a description of two cases3
Postoperative intensive care management and residual endocrinopathy of pediatric supratentorial brain tumors: a retrospective cohort study3
Anxiety, pediatric type 1 diabetes and COVID-19 lockdown3
Expanded phenotypic spectrum in MODY 5 patients with 17q12 deletion syndrome: experience from an Indian tertiary care hospital3
Frontmatter3
Dehydroepiandrosterone sulfate levels at 7 years old and cardio-metabolic factors at 10 and 13 years old – the generation XXI birth cohort3
Identifying elevated plasma free triiodothyronine levels: age-adapted reference intervals for pediatrics3
Frontmatter3
IGAm: A novel index predicting long-term survival in patients with early-diagnosed inherited metabolic disorders3
Increased anxiety symptoms in pediatric type 1 diabetes during the acute phase of COVID-19 lockdown3
Familial early-onset obesity in Turkish children: variants and polymorphisms in the melanocortin-4 receptor (MC4R) gene3
Successful telehealth transformation of a pediatric outpatient obesity teaching program due to the COVID-19 pandemic – the “Video KiCK” program3
A very rare cause of hypertrygliseridemia in infancy: a novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene3
GM1 gangliosidosis: patients with different phenotypic features and novel mutations3
A single-centre study of genetic mutations, audiology, echocardiogram and pulmonary function in Saudi children with osteogenesis imperfecta3
Refractory hypothyroidism in children: an overview3
Molecular and clinical findings of Turkish patients with hereditary fructose intolerance3
Tissue concentration of aldosterone in fetal adrenals of intrauterine death cases3
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 def3
Standard and high dose ergocalciferol regimens for treatment of hypovitaminosis D in epileptic children and adolescents3
Thyroid function tests of iodine deficiency goiter can mimic thyroid hormone resistance alpha3
Frontmatter3
A 10-year retrospective single-center study of alpha-fetoprotein and beta-human chorionic gonadotropin in Romanian children with (para)gonadal tumors and cysts3
Arterial hypertension is associated with an increased risk of metabolic complications in pediatric patient with obesity3
Utility of head CT scan in treatment decisions for suspected cerebral edema in children with DKA3
The therapeutic effect of oral desmopressin lyophilisate formulation in children with central diabetes insipidus3
Computed tomography–guided percutaneous cryoablation of hereditary adrenal pheochromocytoma in three patients3
The effect of gonadotropin-releasing hormone analog treatment on the endocrine system in central precocious puberty patients: a meta-analysis2
Low HDL-C is a non-fasting marker of insulin resistance in children2
Growth response to growth hormone (GH) treatment in children with GH deficiency (GHD) and those with idiopathic short stature (ISS) based on their pretreatment insulin-like growth factor 1 (IGFI) leve2
Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta2
Evaluation of the risk factors for noncommunicable diseases in patients with inborn errors of amino acid metabolism receiving nutrition therapy2
Trajectory of the body mass index of children and adolescents attending a reference mental health center2
Effect of insulin resistance on lung function in asthmatic children2
Clinical manifestations and molecular genetics of seven patients with Niemann–Pick type-C: a case series with a novel variant2
Acquired idiopathic isolated ACTH deficiency with associated autoimmune thyroiditis in pediatrics: case report and review of the literature2
Clinical and laboratory characteristics of propionic acidemia in a Turkish cohort2
Childhood obesity as a safeguarding issue: positive experiences with the “new home” environment as a treatment for weight management2
Frontmatter2
Efficacy of aromatase inhibitor therapy in a case with large cell calcifying Sertoli cell tumour-associated prepubertal gynaecomastia2
Association between overweight or obesity and vitamin D status in preschool children: an epidemiological survey in Beijing, China, 2021–20232
Identification of three novel pathogenic mutations in cystathionine beta-synthase gene of Pakistani intellectually disabled patients2
The smallest dislocated microduplication of Xq27.1 harboring SOX3 gene associated with XX male phenotype2
Size-adjustment techniques of lumbar spine dual energy X-ray absorptiometry measurements in assessing bone mineralization in children on maintenance hemodialysis2
The attitudes, experiences, and self-competencies of pediatric endocrinology fellows and attending physicians regarding diabetes technology: the Turkey experience2
Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty2
Expected or unexpected clinical findings in liver glycogen storage disease type IX: distinct clinical and molecular variability2
Management of perinatal HPP during critical illness/ECMO2
Outcomes of newborns screened for congenital hypothyroidism in Turkey – a single center experience2
Struggle for the future health of adolescent patients with phenylketonuria and parents with a sick child due to the economic crisis2
Clinical characteristics of polyglandular autoimmune syndromes in pediatric age: an observational study2
Aromatase deficiency in an Ontario Old Order Mennonite family2
Severe loss of adipose tissue in a Vietnamese lipodystrophy patient caused by LMNA p.G465D mutation: a first clinical characterization and two-year follow-up2
Diagnostic approach in 46, XY DSD: an endocrine society of bengal (ESB) consensus statement2
Early blood glucose screening in asymptomatic high-risk neonates2
Features of liver injury in 138 Chinese patients with NICCD2
Adiposity rebound in very-low-birth-weight infants2
Excessive weight gain among preschool children during the COVID-19 lockdown in China: a retrospective observational study2
Differentiating true precocious puberty and puberty variants in consecutive 275 girls: a single center experience2
The relationship between estrogen and subsequent growth restriction among adolescents with heavy menstrual bleeding at menarche2
Influence of excess weight on metabolic risk factors in Argentinian preschool children2
Thyroid hormone resistance and large goiter mimicking infiltrative carcinoma in a pediatric patient2
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, Libya2
Relationship between urinary sodium excretion and bone mineral density in pediatrics: population-based study from KNHANES V 2010–20112
Hsa_circ_0002473 inhibits GH3 cell proliferation and GH secretion as a competitive endogenous RNA for has-miR-4645-3p2
Rituximab therapy in ROHHAD(NET) syndrome2
Health related quality of life is associated with gastroesophageal reflux symptoms in overweight children2
A major health problem facing immigrant children: nutritional rickets2
Barth syndrome with severe dilated cardiomyopathy and growth hormone resistance: a case report2
Mental and somatic health in university students with type 1 diabetes: new results from DiaSHoT18, a cross sectional national health and well-being survey2
Late diagnosis of the X-linked MCT8 deficiency (Allan–Herndon–Dudley syndrome) in a teenage girl with primary ovarian insufficiency2
Disordered eating and behaviors among young Egyptians with type 1 diabetes: risk factors and comorbidities2
DSD/intersex: historical context and current perspectives2
Levels of physical activity and barriers to sport participation in young people with gender dysphoria2
Evaluation of patients with phenylalanine metabolism disorder: a single center experience2
Reverse circadian glucocorticoid treatment in prepubertal children with congenital adrenal hyperplasia2
No pubertal growth spurt, rapid bone maturation, and menarche post GnRHa treatment in girls with precocious puberty2
Universal salt iodization potentially contributes to health equity: socio-economic status of children does not affect iodine status2
Timing of onset of menses after GnRH agonist treatment for central precocious puberty2
Associated autoimmune thyroid diseases in children and adolescents with type one diabetes in Jordan2
Clinical characteristics and outcome of hospitalized children and adolescent patients with type 1 diabetes during the COVID-19 pandemic: data from a single center surveillance study in Egypt2
Effects of vitamin D supplementation on glycemic control of children and adolescents with type 1 diabetes mellitus: a systematic review2
Neonatal severe hyperparathyroidism with inactivating calcium sensing receptor (CaSR) mutation (p.I81K)2
Evaluation of metabolic parameters and aortic elasticity in normotensive children with premature adrenarche2
Diagnostic value of fasting insulin and insulin-like growth factor-1 levels in girls with central precocious puberty2
A case report of odonto-hypophosphatasia with a novel variant in the ALPL gene2
The association between vitamin D levels and metabolic syndrome components among metropolitan adolescent population2
The presentation of congenital adrenal hyperplasia in an unscreened population2
Long-term efficacy and safety of PEGylated recombinant human growth hormone in treating Chinese children with growth hormone deficiency: a 5-year retrospective study2
Ovarian hyperthecosis in adolescent females: two case reports and a review of the literature2
One half-century of advances in the evaluation and management of disorders of bone and mineral metabolism in children and adolescents2
Variant in the allosteric domain of CPS1 protein associated with effectiveness of N-carbamoyl glutamate therapy in neonatal onset CPS1 deficiency2
Benefits of metformin add-on insulin therapy (MAIT) for HbA1c and lipid profile in adolescents with type 1 diabetes mellitus: preliminary report from a double-blinded, placebo-controlled, randomized c2
Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidism2
Longitudinal assessment of auxological parameters, adult height outcome and its determinants in leuprolide-treated Indian girls with idiopathic central precocious puberty2
Estrogen-insensitivity syndrome (EIS) in a female adolescent patient – a case report2
Increased frequency of idiopathic central precocious puberty in girls during the COVID-19 pandemic: preliminary results of a tertiary center study2
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