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期刊名:Pediatric endocrinology, diabetes and metabolism

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ISSN:2081-237X

e-ISSN:2083-8441

IF/分区:0.0/

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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
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Introduction: Graves' disease (GD) and autoimmune hepatitis (AIH) represent distinct autoimmune disorders affecting the thyroid and liver, respectively. C...
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Introduction: Dysmorphic syndromes are characterised by congenital anomalies affecting craniofacial features, body proportions, and organ structure. They are frequently caused by complex genetic alterations, including del...
Rita Gomes Alvelos,Paula Santos,Mariana Sebastião et al. Rita Gomes Alvelos et al.
Introduction: Type 1 diabetes mellitus (T1D) is one of the most common chronic diseases in childhood, with its incidence increasing globally. The coronavirus disease 2019 (COVID-19) pandemic has been associated with an in...
Ach Taieb,Omrani Maissa,Ammar Asma et al. Ach Taieb et al.
The insulin tolerance test (ITT) is the most reliable method for diagnosing growth hormone deficiency (GHD). Our study aimed to determine a new glycemic threshold that allows for an adequate growth hormone (GH) response without increasing t...
Piotr Zieliński,Piotr Czeczot,Karolina Góralczyk-Czeczot Piotr Zieliński
This article examines the legal and ethical obligations of physicians towards minor patients with type 1 diabetes in situations where their legal representatives hinder or prevent treatment. This issue is gaining importance in the context o...
Azzeddine Laaraje,Abdelilah Radi,Aomar Agadr et al. Azzeddine Laaraje et al.
Congenital hyperinsulinism (CHI) represents a complex group of genetic disorders causing inappropriate insulin secretion. We report the first case of severe CHI caused by a novel combination of HADH and GHSR mutations, leading to an unusual...
Azzeddine Laaraje,Khadija Abassi,Abdelilah Radi et al. Azzeddine Laaraje et al.
We report a 12-year-old girl with developmental delay, dysmorphic features, and short stature initially diagnosed with growth hormone deficiency at age 7. Despite appropriate growth hormone treatment for four years with documented insulin-l...
Olga Kamińska-Jackowiak,Martyna Kolasa,Agata Chobot et al. Olga Kamińska-Jackowiak et al.
Introduction: The study aimed to systematically evaluate whether coronavirus disease (COVID-19) infection and/or vaccination act as environmental triggers for new-onset type 1 diabetes (T1D) in children and adolescents. ...
Julia Gąsiorowska,Amelia Grundys,Laura Gawlik et al. Julia Gąsiorowska et al.
Introduction: Excessive growth syndromes are a heterogeneous group of rare congenital disorders characterized by increased body size from the neonatal period or early childhood. In addition to accelerated growth, these co...