XLH Matters 2024: expert insights and practical tools for enhancing care of people living with X-linked hypophosphataemia.

IF 3.5 2区医学 Q2 GENETICS & HEREDITY

Orphanet Journal of Rare Diseases Pub Date : 2025-09-18 DOI:10.1186/s13023-025-03930-x

Lothar Seefried, Ali S Alzahrani, Carsten A Wagner, Damian Eade, Danilo Fintini, Dieter Haffner, Hasan Frookh Jamal, Judith S Bubbear, Laura Guazzarotti, Moira S Cheung, Noina Abid, Patrícia Costa-Reis, Rui Ferreira Santos, Signe Sparre Beck-Nielsen, Agnès Linglart

引用次数: 0

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XLH Matters 2024：加强对x连锁低磷血症患者护理的专家见解和实用工具。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Orphanet Journal of Rare Diseases 医学-医学：研究与实验

CiteScore

6.30

自引率

8.10%

发文量

418

审稿时长

4-8 weeks

期刊介绍： Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.