Hormone Research in Paediatrics

Papers
(The median citation count of Hormone Research in Paediatrics is 1. 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 2021-09-01 to 2025-09-01.)
ArticleCitations
Congenital Hyperinsulinism: An Historical Perspective50
Congenital hyperinsulinism of a large Italian cohort: a retrospective study45
The Digital-Human Interface: An Essential Combination for Clinical Progress41
Do Changes in BMI during the COVID-19 Pandemic Persist in the Post-Pandemic Period in a Pediatric Population Attending Health Care Clinics? A Longitudinal Study36
Contents Vol. 96, 202333
The Evaluation and Management of Methimazole-Induced Agranulocytosis in the Pediatric Patient: A Case Report and Review of the Literature32
Rhabdomyolysis: A Rare Presentation of Hashimoto Thyroiditis in an Adolescent Boy and Review of the Literature31
Growth and Growth Hormone through the Ages: Art and Science31
A New Variant in the <i>GATA6</i> Gene Associated with Tracheoesophageal Fistula, Pulmonary Vein Stenosis, and Neonatal Diabetes29
Contribution of Sex Steroids in Management of Tall Stature: Is it Effective or Not?28
Enhancing Care in Type 1 Diabetes with Artificial Intelligence Driven Clinical Decision Support Systems27
Parental Perception of Quality of Life and Impact of Short Stature in Children with Hypochondroplasia and other Genetic Causes of Short Stature26
Rarity of congenital adrenal hyperplasia in children born very preterm:Possible mechanism and implication for newborn screening22
Erratum21
Phenotype-Genotype Correlations of <i>GH1</i> Gene Variants in Patients with Isolated Growth Hormone Deficiency or Multiple Pituitary Hormone Deficiency21
Endocrine Comorbidities in Survivors of Childhood Brain Tumors: Insights from the Slovenian National Cohort20
Management of Arginine Vasopressin Deficiency (Central Diabetes Insipidus) in Neonates and Infants20
The Influence of X Chromosome Parent-of-Origin on Glycemia in Individuals with Turner Syndrome20
Establishing a Molecular Genetic Diagnosis in Children with Differences of Sex Development: A Clinical Approach19
The Long Path to Our Current Understanding Regarding Care of Children with Differences/Disorders of Sexual Development19
Glucagon-Like Peptide-1 Receptor Agonists in the Treatment of Obesity19
Front & Back Matter18
Venous Thrombosis in a Pseudohypoparathyroidism Patient with a Novel <i>GNAS</i> Frameshift Mutation and Complete Resolution of Vascular Calcifications with Acetazolamide Treatment18
Growth Hormone Dose Modulation and Final Height in Short Children Born Small for Gestational Age: French Real-Life Data17
Review of Implant Gonadotrophin-Releasing Hormone Agonist Use: Experience in a Single Academic Center17
Recurrent Intracranial Hypertension in a Toddler with Graves’ Disease17
Clinical Characteristics of Children with <i>THRA</i> Mutations: Variable Phenotype and Good Response to Recombinant Human Growth Hormone Therapy17
Team Based Pediatric Type 1 Diabetes Care in the US: Current Practices and Sustainability Concerns16
Schaaf-Yang Syndrome: Clinical Phenotype and Effects of 4 years of Growth Hormone Treatment16
Beneficial Effects of RESMENA Diet on Anthropometric, Metabolic, and Reproductive Profile in Adolescents with Obesity and Polycystic Ovary Syndrome: A Randomized Controlled Intervention Study15
ISPAD Clinical Practice Consensus Guidelines 2024: Type 2 Diabetes in Children and Adolescents15
Epigenetics of childhood obesity14
Delayed Puberty Phenotype Observed in Noonan Syndrome Is More Pronounced in Girls than Boys14
Long-term treatment for Laron syndrome with IGF-1 injection over 22 years in Saudi: A cohort study14
ADECA: A novel course for training Paediatric Diabetes Nurse Educators in Sub-Saharan Africa14
Infants with Congenital Adrenal Hyperplasia Exhibit Thalamic Discrepancies in Early Brain Structure14
The Evolution of Adolescent Gender-Affirming Care: An Historical Perspective14
Burosumab Therapy in a Paediatric Patient with McCune-Albright Syndrome: A Case Report13
Variability in Body Mass Index during 2018–2021 for People with Type 1 Diabetes: Real World Data from the USA, Germany, and Australasia13
Sodium-Glucose Co-Transporter-2 Inhibitors in Type 1 Diabetes: A Scoping Review13
Noonan Syndrome Growth Charts and Genotypes: 15-Year Longitudinal Single-Centre Study12
Children with Growth Hormone Deficiency Treated With Lonapegsomatropin Demonstrated Sustained Height Improvements for up to 6 Years- enliGHten Trial Final Results12
Pros and Cons of Current Diagnostic Tools for Risk-Based Screening of Prediabetes and Type 2 Diabetes in Children and Adolescents with Overweight or Obesity12
Ways to Improve the Diagnosis of Growth Hormone Deficiency11
Nathalie Josso, MD, PhD, 1934–202211
Efficacy and Safety of Once-Weekly Somatrogon Compared with Once-Daily Somatropin (Genotropin®) in Japanese Children with Pediatric Growth Hormone Deficiency: Results from a Randomized Phase 3 Study11
Clinical Predictors of Good/Poor Response to Growth Hormone Treatment in Children with Idiopathic Short Stature11
Functional Characterization of Thyroid Peroxidase Missense Variants Causing Thyroid Dyshormonogenesis in Asian Indian Population11
A Pediatric Case of Reninoma Presenting with Paraneoplastic Syndrome of Inappropriate Antidiuretic Hormone Secretion11
The Effect of Pre-Thyroidectomy Calcitriol Prophylaxis on Post-Thyroidectomy Hypocalcaemia in Children11
A Critical Review of Upcoming New Therapeutic Options in Paediatric Endocrinology10
Five-Year Therapy with Recombinant Human Insulin-Like Growth Factor-1 in a Patient with PAPP-A2 Deficiency10
Obesity Is Associated with Increased 11-Oxyandrogen Serum Concentrations during Puberty10
Health-Related Quality of Life of Young Adult Women with a History of Premature Adrenarche10
Phase 2 Trial of Vosoritide Use in Patients with Hypochondroplasia: A Pharmacokinetic/Pharmacodynamic Analysis10
Genetic Obesity in Children: Overview of Possible Diagnoses with a Focus on <b><i>SH2B1</i></b> Deletion9
The ADHventures of Asterix and Copeptin: The Hyponatraemia Challenge9
Case report and literature review: A 46, XX infant with atypical genitalia diagnosed with primary ovarian insufficiency (POI) caused by HFM1 gene variants9
Outcome of Dopamine Agonist Therapy Withdrawal in Children with Prolactinomas9
Front & Back Matter9
Subject Index Vol. 96, No. 6, 20239
A Novel Pathogenic Variant in <i>Fibroblast Growth Factor 23</i> outside the Furin-Recognizing RXXR Motif in an Autosomal Dominant Hypophosphatemic Rickets Patient9
Challenges in Hypophosphatasia: Suspicion, Diagnosis, Genetics, Management, and Follow-Up9
Measuring Adolescent Chronic Stress: A Review of Established Biomarkers and Psychometric Instruments8
Reply to Letter: Ways to Improve the Diagnosis of Growth Hormone Deficiency8
Somapacitan is Effective and Well Tolerated in Chinese Children with Growth Hormone Deficiency: a Randomised Controlled Phase 3 Study8
11th International Meeting of Paediatric Endocrinology (IMPE) - Abstracts8
Variants of Unknown Significance (VUS) in Maturity-Onset Diabetes of the Young (MODY): High Rate of Conundrum Resolution via VUS Reanalysis8
I-DSD: The First 10 Years8
Sensitivity to Thyroid Hormones and Reduced Glomerular Filtration in Children and Adolescents with Overweight or Obesity8
ISPAD Clinical Practice Guidelines 2024: Editorial8
Early Nutrition and Later Excess Adiposity during Childhood: A Narrative Review7
Diagnostic Conundrum of a Sertoli Cell Tumor in a 2-Year-Old Girl with Peripheral Precocious Puberty and a Café-au-Lait Macule: A Case Report7
Relation between the Epicardial Fat Thickness and the Cardiac Conduction System in Children and Adolescents with Diabetes7
Preliminary Pages7
Automated Insulin Delivery Systems for Treatment of Type 1 Diabetes: Strategies for Optimal Performance7
Familial Non-autoimmune Hyperthyroidism Caused by an Extracellular Domain Variant (p.Leu267Phe) of the TSH Receptor.7
Hepatic Steatosis and Stiffness in Adolescent Obesity are Linked to Androgenemia, Insulin Sensitivity, and Inflammation7
Histopathological Criteria for Paediatric Adrenocortical Carcinoma7
ISPAD Position Statement on Type 1 Diabetes in Schools7
Novel Calcium-Sensing Receptor (CASR) Mutation in a Family with Autosomal Dominant Hypocalcemia Type 1 (ADH1): Genetic Study over Three Generations and Clinical Characteristics7
ISPAD Clinical Practice Consensus Guidelines 2024: Glycemic Targets6
Stress and Growth in Children and Adolescents6
A Scoping Review of Literature Exploring the Healthcare Transition of Individuals with Congenital Adrenal Hyperplasia6
An Overlooked Manifestation of Hypercortisolism: Cerebral Cortical Atrophy and Challenges in Identifying the Etiology of Hypercortisolism – A Report of 2 Pediatric Cases6
Erratum6
Successful Use of Metyrapone Suppositories in an Infant with Neonatal Cushing and McCune Albright Syndrome: A Case Report6
Effects of a 2-Year Early Childhood Vitamin D<sub>3</sub> Intervention on Tooth Enamel and Oral Health at Age 6–7 Years6
Acquired Generalized Lipodystrophy with Extensive Autoimmune Involvement: A Case Report and Review of the Literature6
Prospective Test Performance of Nonfasting Biomarkers to Identify Dysglycemia in Children and Adolescents6
Raised Thyroid-Stimulating Hormone in Girls with Polycystic Ovary Syndrome: Effects of Randomized Interventions6
Patient and Parent Perspectives on Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia6
Strategies for Equitable Recruitment to Engage Underrepresented Youth and Their Families into Clinical Research: Findings from the BEAD-T1D Pilot Study6
Weekly Growth Hormone (Lonapegsomatropin) Causes Severe Transient Hyperglycemia in a Child with Obesity6
Erratum5
Congenital Hyperinsulinism and Long QT Syndrome Attributable to a Variant in KCNE15
Subtotal Parathyroidectomy Successfully Controls Calcium Levels of Patients with Neonatal Severe Hyperparathyroidism Carrying a Novel CASR Mutation5
DHX37 and the Implications in Disorders of Sex Development: An Update Review5
Characterization of Digestive Manifestations in Patients with Impaired PTH/PTHrP Signaling Disorder/Pseudohypoparathyroidism5
Author- and Subject Index5
Novel Insights: A Novel PHIP Variant in a Family with Severe Early-Onset Obesity5
Metabolic Changes across Tertiles of Delta Changes in Height SDS during Growth Hormone Therapy in Children with Growth Hormone Deficiency5
Neural Correlates of Obesity and Inflammation in Children and Adolescents with Congenital Adrenal Hyperplasia5
The Role of DLK1 Deficiency in Central Precocious Puberty and Association with Metabolic Dysregulation5
Copeptin Stimulation by Combined Intravenous Arginine and Oral LevoDopa/Carbidopa in Healthy Short Children and Children with the Polyuria-Polydipsia Syndrome5
The Association between Vitamin D Deficiency and Hepatosteatosis in Children and Adolescents with Obesity5
Polygenic Childhood Obesity: Integrating Genetics and Environment for Early Intervention5
Erratum5
Management of Acute Adrenal Insufficiency-Related Adverse Events in Children with Congenital Adrenal Hyperplasia: Results of an International Survey of Specialist Centres5
Regional deprivation and diabetic ketoacidosis at type 1 diabetes diagnosis in children and adolescents: International comparison among 6 countries5
Long-Acting Growth Hormone Preparations and Their Use in Children with Growth Hormone Deficiency5
Stress, Stress Reduction and Obesity in Childhood and Adolescence5
Subject Index5
Ovotesticular Difference of Sex Development: Genetic Background, Histological Features, and Clinical Management5
Thioredoxin Reductase 2 Variant as a Cause of Micropenis, Undescended Testis, and Selective Glucocorticoid Deficiency4
Invited Mini Review Metabolic Bone Disease of Prematurity: Overview and Practice Recommendations4
Cross-Cultural Disparities in Psychosocial Research with Individuals with Classical Congenital Adrenal Hyperplasia: A Scoping Review4
International Newborn Screening Practices for the Early Detection of Congenital Adrenal Hyperplasia4
Subject Index4
Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features4
Finding early biomarkers to prevent unfavorable long-term health outcomes after premature adrenarche – a multicenter prospective cohort study protocol4
Thyrotoxic hypokalemic periodic paralysis induced by high-dose insulin in an adolescent male with type 1 diabetes mellitus4
Differential Methylation of CYP11B1 in Girls with High DHEAS Levels and correlation with 11-Oxyandrogen levels: a pilot study4
Safety and Efficacy of Bilateral Epiphysiodesis Surgery to Reduce Final Height in Extremely Tall Adolescents: A Follow-Up Study4
Novel Use of Dasiglucagon, a Soluble Glucagon Analog, for the Treatment of Hyperinsulinemic Hypoglycemia Secondary to Suspected Insulinoma: A Case Report4
The Evidence for Twice-Daily Hydrocortisone Dosing in Children with Congenital Adrenal Hyperplasia Is Lacking4
Front & Back Matter4
A Brief History of the Pediatric Endocrine Society (PES)4
Up-to-Date Clinical and Biochemical Workup of the Child and the Adolescent with a Suspected Disorder of Sex Development4
Gut Hormones Secretion across Clusters of Metabolic Syndrome in Prepubertal Children with Obesity4
Prelims4
Bariatric Surgery in Adolescents with Obesity: Long-Term Perspectives and Potential Alternatives4
Endocrine management of transgender and gender diverse adolescents: expert opinion of the ESPE Working Group on Gender Incongruence and the Endo-ERN main thematic group on Sexual Development and Matur4
Managing Children and Adolescents with Type 1 Diabetes and Coexisting Celiac Disease: Real-World Data from a Global Survey3
Novel Treatment Options in Childhood Bone Diseases3
Twenty Years of Neonatal Screening for Congenital Adrenal Hyperplasia in North-Eastern Italy: Role of Liquid Chromatography-Tandem Mass Spectrometry as a Second-Tier Test3
In Memoriam: Werner Friedrich Paul Blum, 1949–20243
Short stature and response to growth hormone treatment in CUL3-related neurodevelopmental disorder3
Moving from Insulin Substitution to the Treatment of the Underlying Autoimmune Disease in Type 1 Diabetes3
Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature3
Improving Anxiety Screening in Patients with Turner Syndrome3
Subject Index Vol. 95, No. 6, 20223
Metabolic and bariatric surgery in adolescents: a single-center study of efficacy and outcome predictors3
Fetal Thyrotoxicosis due to Maternal TSH Receptor Stimulating Antibodies Causes Infant Central Hypothyroidism3
Vascular Complications in Children and Young People with Type 1 Diabetes: A Worldwide Assessment of Diabetologists’ Adherence to International Recommendations3
Pigmented Hypertrichosis with Insulin-Dependent Diabetes Mellitus Syndrome: A Case Series3
Impact of Stress on Health in Childhood and Adolescence3
Growth and Treatment in Congenital Adrenal Hyperplasia: An Observational Study from Diagnosis to Final Height3
Real-World Safety and Effectiveness of Vosoritide in Children with Achondroplasia: French Early Access Program3
Cardiovascular Risk Factors in Children and Adolescents with Type 1 Diabetes Mellitus: The Role of Insulin Resistance and Associated Genetic Variants3
Response to “Invited Mini Review Metabolic Bone Disease of Prematurity: Overview and Practice Recommendations” – Limitations to Utilization of Practice Guideline in Acutely Ill and Medically Complex N3
Longitudinal Changes in Acylated versus Unacylated Ghrelin Levels May Be Involved in the Underlying Mechanisms of the Switch in Nutritional Phases in Prader-Willi Syndrome3
Molecular Genetic Analysis and Growth Hormone Treatment in a Three-Generation Chinese Family with Tricho-Rhino-Phalangeal Syndrome I3
Surveying Current Practices in the Use of Gadolinium-Based Contrast Agents for Routine Brain Magnetic Resonance Imaging in the Evaluation of Isolated Growth Hormone Deficiency among US Pediatric Endoc3
Evaluating Eating Behaviour, Energy Homeostasis, and Obesity in Childhood-Onset Craniopharyngioma: A Feasibility Study3
Association between Endocrine Disorders and Severe COVID-19 Disease in Pediatric Patients3
Front & Back Matter3
Copeptin: Utility in Paediatric Patients with Hyponatraemia3
Persistent Hypoglycemia in Diabetes Type 1 Patient with Medtronic 780 G Insulin Pump: A Case Report3
Cell Therapy for Type 1 Diabetes: From Islet Transplantation to Stem Cells3
Prenatal diagnosis of autosomal dominant pseudohypoaldosteronism due to NR3C2 gene mutation. Immediate post-natal oral saline therapy prevents the clinical manifestations resulting from impaired salt 3
Arginine-Stimulated Copeptin-Based Diagnosis of Central Diabetes Insipidus in Children and Adolescents3
Urinary Bisphenol A and Bis(2-Ethylhexyl) Phthalate Metabolite Concentrations in Children with Obesity: A Case-Control Study3
Subject Index Vol. 96, No. 1, 20233
Physical Activity in Very Young Children living with Type 1 diabetes3
Feasibility of using continuous glucose monitoring to detect glycemic abnormalities in children with cystic fibrosis.2
The Timing of Genital Surgery in Somatic Intersexuality: Surveys of Patients’ Preferences2
Challenges in Beta Cell Replacement for Type 1 Diabetes2
Recognition of Hyperinsulinaemic Hypoglycaemia in Infants with Congenital Central Hypoventilation Syndrome2
Insulin-Induced Copeptin Response in Children and Adolescents to Diagnose Arginine Vasopressin Deficiency2
Timing of Meal Consumption on Glucose Profiles in Latino Adolescents with Obesity2
Genotype-phenotype correlation and feminizing surgery in Danish children with congenital adrenal hyperplasia2
Front & Back Matter2
Unmet Needs of Pediatricians in Transgender-Specific Care: Results of a Short-Term Training2
Abstracts of the 2024 Pediatric Endocrine Society (PES) Annual Meeting. Chicago, IL, May 2 – 5, 20242
Hypothyroidism in infants after enteral administration of iodinated contrast media: a rare but serious complication2
Clinical Characteristics of Pathogenic ACAN Variants and 3-Year Response to Growth Hormone Treatment: Real-World Data2
Diagnostic Utility of Low-Dose Cosyntropin Stimulation Test for Central Adrenal Insufficiency2
Multi-Stakeholder Opinion Statement on the Care of Individuals Born with Differences of Sex Development: Common Ground and Opportunities for Improvement2
Development of a Minimum Dataset for the Monitoring of Recombinant Human Growth Hormone Therapy in Children with Growth Hormone Deficiency: A GloBE-Reg Initiative2
Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets2
Post-Menarcheal Growth Patterns in a Contemporary Cohort of Latino Girls2
Adrenal Cushing Syndrome: Diagnosis and Management in a 10-Year-Old Boy with Carney Complex2
Front & Back Matter2
Assessment of Nutritional Status in the Diagnostic Evaluation of the Child with Growth Failure2
Cortisol Dynamics, Quality of Life, and Fatigue following Traumatic Brain Injury in Childhood2
Vitamin D Toxicity from an Unusual and Unexpected Source: A Report of 2 Cases2
Fertility Counseling Practices for Patients with Turner Syndrome in Pediatric Endocrine Clinics: Results of a Pediatric Endocrine Society Survey2
Demystifying Skeletal Dysplasias: A Practical Approach for the Pediatric Endocrinologist2
Nocturnal Salivary Cortisol Is an Accurate Non-Invasive Test to Assess Endogenous Hypercortisolism in Children with Obesity and a Clinical Phenotype Suspicious for Cushing’s Syndrome2
Long-Term Retention of Young Adult Study Participants with Youth-Onset Type 2 Diabetes: Results from the TODAY2 Study2
DHX37 Variant Is One of the Common Genetic Causes in Japanese Patients with Testicular Regression Syndrome/Partial Gonadal Dysgenesis without Müllerian Derivatives2
Potential for Optimization of Growth Hormone Treatment in Children with Growth Hormone Deficiency, Small for Gestational Age, and Turner Syndrome in Germany: Data from the PATRO<sup>®</sup>2
Erratum2
Genetic Findings in Short Turkish Children Born to Consanguineous Parents2
Short Stature and Distinct Growth Characteristics in Angelman Syndrome2
Erratum2
Non malignant ACTH-Independent Cushing Syndrome in Pediatric Patients: A Retrospective Observational Cohort Study2
Can GH Therapy Worsen a Clinically Silent Chiari Malformation? A Case Report and Systematic Literature Review2
Congenital Central Hypothyroidism Caused by a Novel IGSF1 Variant Identified in a French Family1
Co-occurrence of DNET and Hodgkin's Lymphoma in a patient with Noonan syndrome and mutation in the PTPN11 gene1
Contents Vol. 95, 20221
Effects and Safety of Growth Hormone Treatment in Six Children with Pycnodysostosis1
Is Growth Hormone Therapy for Previously Small for Gestational Age Safe and Effective? Commentary on Results from the 2005–2018 French National Registry1
Neurodevelopmental Follow-Up of Children Born to Mothers with Graves’ Disease and Neonatal Hyperthyroidism1
History of the Thyroid1
Adult Height of Patients with <b><i>SHOX</i></b> Haploinsufficiency with or without GH Therapy: A Real-World Single-Center Study1
Blood Pressure in Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency1
Chronic Stress and Steatosis of Muscles, Bones, Liver, and Pancreas: A Review1
The Utility of Copeptin Measurement in Hospitalized Pediatric Patients with SIADH1
Salivary 17-Hydroxyprogesterone Levels in Children with Congenital Adrenal Hyperplasia: A Retrospective Longitudinal Study Considering Auxological Parameters1
Use of aromatase inhibitors in short children and adolescents to increase height gain: A current practice survey and review of the literature1
Indeterminate Thyroid Fine-Needle Aspirations in Pediatrics: Exploring Clinicopathologic Features and Utility of Molecular Profiling1
A dual etiology of neonatal hypoglycemia secondary to FOXA2 heterozygous deletion1
Prolonged Pubertal Suppression due to Retained Histrelin Implant in Three Children with Central Precocious Puberty1
XXX Annual Meeting of the Latin American Pediatric Endocrinology Society (SLEP) Bogota, Colombia, October 19-22, 20221
ISPAD Annual Conference Highlights 20231
Ten-Year Experience of a Global and Freely Accessible e-Learning Website for Pediatric Endocrinology and Diabetes1
Endocrine-Related Adverse Conditions in Pediatric Patients Treated with Immune Checkpoint Inhibitors: a Position Statement from the Clinical Practice Committee of the European Society for Pediatric En1
Preliminary Pages1
Acute kidney injury at the onset of type 1 diabetes mellitus: a balance between kidney stress and nephron mass1
Stress, Thyroid Dysregulation, and Thyroid Cancer in Children and Adolescents: Proposed Impending Mechanisms1
Prelims1
Potentialities of Gene Therapy in Pediatric Endocrinology1
Preliminary Pages1
Combined Arginine and Insulin Stimulation Elicits a Robust and Consistent Copeptin Response in Short Children1
<b><i>SLIT2</i></b> Rare Sequencing Variants Identified in Idiopathic Hypogonadotropic Hypogonadism1
The Relationship between Metabolic Comorbidities and Post-Surgical Weight Loss Outcomes in Adolescents Undergoing Laparoscopic Sleeve Gastrectomy1
Characteristics of Patients with Classic Congenital Adrenal Hyperplasia Missed on the Newborn Screen1
Thyroid Ultrasound Screening in Childhood Cancer Survivors following Radiotherapy1
Novel Insights into the Pathophysiology and Management of Obesity in Childhood and Adolescence1
Erratum1
SKIN-PEDIC – a worldwide assessment of skin problems in children and adolescents using diabetes devices1
Serum Calcium Normal Range in 1,000 Term Newborns1
Key Stages in the Development and Establishment of Paediatric Endocrinology: A Template for Future Progress1
Celebrating 50 Years of the Pediatric Endocrine Society (PES): Histories of Pediatric Endocrine Topics1
Prevalence of Polycystic Ovarian Syndrome in Girls with a History of Idiopathic Central Precocious Puberty1
Drivers of Patient and Caregiver Preferences for Growth Hormone Deficiency Treatments in France: A Discrete Choice Experiment1
Erratum1
Reversible Hypothalamic Obesity in a Girl with Suprasellar Tuberculoma1
Novel Adipokines <b><i>CTRP1</i></b>, <b><i>CTRP9</i></b>, and <b><i>FGF21</i></b> in Pediatric Type 1 and Type 2 Diabetes: A Cr1
Global Adrenal Insufficiency in Two Independent Patients Carrying the Same Homozygous c.172A&gt;G, p.(Thr58Ala) Mutation in the <i>TBX19</i> Gene1
ISPAD Clinical Practice Consensus Guidelines 2024: Screening, Staging, and Strategies to Preserve Beta-Cell Function in Children and Adolescents with Type 1 Diabetes1
A <i>Novel RNPC3</i> Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy1
Care for Transgender Young People1
Sex Hormone Treatment for Female Children and Young Adults with Disorders Affecting Hypothalamic, Pituitary, and Ovarian Function1
Early Life Stress, Hormones, and Neurodevelopmental Disorders1
Front & Back Matter1
Accelerated Linear Growth during Erdafitinib Treatment: An FGFR-Related, but Growth Factor and Sex Steroid-Independent Mechanism?1
The Half-Empty Glass of GH Treatment in Dyschondrosteosis1
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