Hormone Research in Paediatrics

Papers
(The TQCC of Hormone Research in Paediatrics is 4. 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
Growth and Growth Hormone through the Ages: Art and Science31
Rhabdomyolysis: A Rare Presentation of Hashimoto Thyroiditis in an Adolescent Boy and Review of the Literature31
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
Phenotype-Genotype Correlations of <i>GH1</i> Gene Variants in Patients with Isolated Growth Hormone Deficiency or Multiple Pituitary Hormone Deficiency21
Erratum21
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
Endocrine Comorbidities in Survivors of Childhood Brain Tumors: Insights from the Slovenian National Cohort20
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
Establishing a Molecular Genetic Diagnosis in Children with Differences of Sex Development: A Clinical Approach19
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
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
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
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
ISPAD Clinical Practice Consensus Guidelines 2024: Type 2 Diabetes in Children and Adolescents15
Beneficial Effects of RESMENA Diet on Anthropometric, Metabolic, and Reproductive Profile in Adolescents with Obesity and Polycystic Ovary Syndrome: A Randomized Controlled Intervention Study15
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
Epigenetics of childhood obesity14
Delayed Puberty Phenotype Observed in Noonan Syndrome Is More Pronounced in Girls than Boys14
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
Burosumab Therapy in a Paediatric Patient with McCune-Albright Syndrome: A Case Report13
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
Noonan Syndrome Growth Charts and Genotypes: 15-Year Longitudinal Single-Centre Study12
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
Ways to Improve the Diagnosis of Growth Hormone Deficiency11
Nathalie Josso, MD, PhD, 1934–202211
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
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
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
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
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
Measuring Adolescent Chronic Stress: A Review of Established Biomarkers and Psychometric Instruments8
Reply to Letter: Ways to Improve the Diagnosis of Growth Hormone Deficiency8
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
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
Successful Use of Metyrapone Suppositories in an Infant with Neonatal Cushing and McCune Albright Syndrome: A Case Report6
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
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
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
ISPAD Clinical Practice Consensus Guidelines 2024: Glycemic Targets6
Stress and Growth in Children and Adolescents6
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
Erratum6
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
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
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
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
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