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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
Karine Aouchiche,Mirjam Dirlewanger,Mehul Dattani et al. Karine Aouchiche et al.
Introduction: Pituitary duplication is a rare congenital malformation, with fewer than 80 cases reported in the literature. It is often associated with midline malformations but can also occur in isolation. Central precoc...
Erratum [0.03%] 勘误表
The article "Bone Health in Young Individuals with Primary Ciliary Dyskinesia: Insights from a Comparison with Cystic Fibrosis and Healthy Controls" [Horm Res Paediatr. 2025; https://doi.org/10.1159/000549604] by Gaupmann et al. was publish...
Julio Soto,Katherine Rozas,Alba León et al. Julio Soto et al.
Introduction: Cardiovascular risk factors and depressive symptoms are common in adolescents and young adults with type 1 diabetes (T1D). While exercise improves cardiovascular health and metabolic control, its mental heal...
Laurence Bastien,Mimi S Kim,Cathrine Constantacos et al. Laurence Bastien et al.
Background: Adrenal suppression is a potential side effect of glucocorticoid (GC) therapy. Timely diagnosis and management can significantly reduce morbidity and mortality from adrenal crisis. There is a need for pediatri...
Victoria R Sanders,Katherine Lord,Winnie Sigal et al. Victoria R Sanders et al.
Introduction Congenital hyperinsulinism (HI) may be diazoxide-responsive or diazoxide-unresponsive. Patients with diazoxide-unresponsive HI are further classified based on having the diffuse or focal form of the disease, with different mana...
Varsha Thomas,Natalie Segev,Amy S Shah et al. Varsha Thomas et al.
Introduction: Type 2 diabetes mellitus (T2DM) is more aggressive when diagnosed in childhood, and its incidence continues to rise. Premature adrenarche (PA) is often considered benign; however, emerging data suggest a com...
Roos I van Rhijn,A S Paul van Trotsenburg,Rosaline Mentink Roos I van Rhijn
Introduction: This study aimed to investigate differences in clinical and biochemical characteristics between autoantibody positive and autoantibody negative type 1 diabetes mellitus (T1DM) in children, to get a better un...
Yanqin Ying,Haiyan Wei,Yan Zhong et al. Yanqin Ying et al.
Introduction: Lonapegsomatropin, a prodrug of somatropin, is approved for once-weekly treatment of paediatric growth hormone deficiency (GHD) in the USA and Europe. Here, we report the first trial to assess the efficacy a...
Xinmeng Wang,Zheng Yuan,Miao Qin et al. Xinmeng Wang et al.
Introduction: In 21-hydroxylase deficiency (21-OHD), impaired 21-hydroxylase activity causes 17-hydroxyprogesterone (17-OHP) accumulation and androgen excess, typically manifesting as hyperandrogenism. The POR gene encode...
Enora Le Roux,Kirstine Stochholm,Martin Fassnacht et al. Enora Le Roux et al.
Background: The transition from paediatric to adult healthcare is a critical period for young individuals with endocrine conditions. Despite numerous published recommendations, Europe still lacks recent, comprehensive, ev...