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期刊名:Hormone research in paediatrics

缩写:HORM RES PAEDIAT

ISSN:1663-2818

e-ISSN:1663-2826

IF/分区:3.8/Q1

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共收录本刊相关文章索引1899
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Klara Maliska-Maratova,Katerina Gregorova,Maciej Jaworski et al. Klara Maliska-Maratova et al.
Introduction: Muscle functions are dependent on age, weight and height. The question of how the muscle-bone unit is adapted for tall stature is yet to be elucidated. The aim of this study was to evaluate muscle functions ...
Aman Pulungan,Helena A Puteri,Annisa N Insani et al. Aman Pulungan et al.
Introduction: With Indonesia introducing newborn screening (NBS) for congenital adrenal hyperplasia (CAH) in 2024, it is anticipated that the number of diagnosed CAH cases will rise. Therefore, it is crucial that healthca...
Karine Aouchiche,Pauline Romanet,Théo Charnay et al. Karine Aouchiche et al.
Introduction: Isolated growth hormone deficiency (IGHD) involves multiple genes, yet characterization of its mutational landscape and genotype-phenotype correlations remains limited. The aim of this study is to analyze a ...
Anika S Naidu,Joan C Lo,Jeanne A Darbinian et al. Anika S Naidu et al.
Introduction: Polycystic ovary syndrome (PCOS) is an endocrine disorder that is rising in prevalence among adolescents, attributable in part to the obesity epidemic. PCOS disproportionately affects Asian females, includin...
Joeri Vliegenthart,Iris Vernooij,Eric J E van der Hijden et al. Joeri Vliegenthart et al.
Objective The SEENEZ GH trial found no difference in near adult height (NAH) between patients with isolated idiopathic growth hormone deficiency (IIGHD) who continued or discontinued recombinant human growth hormone (rhGH) at mid‑puberty a...
Gerhard Binder,Desiree Dunstheimer,Bettina Gohlke et al. Gerhard Binder et al.
Background Endocrine disorders appear to be unevenly distributed between females and males in pediatric endocrinology. Summary This narrative review collects causes from nurture and nature that may contribute to these differences in prevale...
Elisabeth Jelleryd,Carmel E Smart,Hans Järnbert-Petterson et al. Elisabeth Jelleryd et al.
Background Carbohydrate counting (CC) for calculating insulin for meals is recommended in type 1 diabetes to optimize the postprandial glycemic response. Few studies have studied the effect of CC on glycemic outcomes when introduced from di...
Elsa Dieterlen,Carine Villanueva,Sara Cabet et al. Elsa Dieterlen et al.
Adrenocortical tumors (ACTs) are rare pediatric malignancies, typically presenting with signs of virilization or hypercortisolism. However, non-classical presentations may delay diagnosis and complicate management. Our study aimed to illust...
Agata Chobot,Artur Bossowski,Przemysława Jarosz-Chobot et al. Agata Chobot et al.
Recent advances in the understanding of the natural history of type 1 diabetes (T1D), together with the availability of disease-modifying therapies, have fundamentally changed the rationale for early detection of this disease. Type 1 diabet...
Eadaoin Hayes,Ann Nillsen,Peter W Rowe et al. Eadaoin Hayes et al.
Introduction: Mitochondrial diabetes is rare and typically treated with dietary intervention and oral hypoglycaemic agents. Most require insulin. Novel treatments are available but are not well-characterised. ...