首页 文献索引 SCI期刊 AI助手
期刊目录筛选

期刊名:Hormone research in paediatrics

缩写:HORM RES PAEDIAT

ISSN:1663-2818

e-ISSN:1663-2826

IF/分区:2.7/Q1

文章目录 更多期刊信息

共收录本刊相关文章索引1865
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
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...
Amelie Perriere,Frédéric Brioude,Marie-Noëlle Dufourg et al. Amelie Perriere et al.
Objective: Silver-Russell syndrome (SRS) is a rare imprinting disorder characterized by growth retardation, early puberty, and poor pubertal growth, leading to short stature. We aimed to assess the outcome in terms of adu...
Joaquim de Matos Cavalcante,Laurana de Polli Cellin,Amanda Latuffe Soares Damião et al. Joaquim de Matos Cavalcante et al.
Context: Evidence for growth hormone therapy in Indian hedgehog (IHH)-related short stature is limited. Objective: To assess growth out...
Nozomi L Yamashita,Edwin A Deras,Sharon H O Apos Neil et al. Nozomi L Yamashita et al.
Introduction: Youth and adults with classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) are at risk for cognitive deficits and brain structural changes. Although factors inherent to CAH...
Garrett I Ash,Soohyun Nam,Selene S Mak et al. Garrett I Ash et al.
Background: Adolescents with type 1 diabetes (T1D) face barriers to moderate-to-vigorous physical activity (MVPA) such as uncertainty with self-management, limited access to supportive environments, and stigma related to ...