XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes.

{"title":"XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes.","authors":"Lothar Seefried, Ferdinando Aliberti, Cathrine Alsaker Heier, Pedro Arango-Sancho, Martin Biosse Duplan, Sophia D Sakka, Francesco Emma, Oliver Gardiner, Muhammad Kassim Javaid, Rui M Ferreira-Santos, Adalbert Raimann, Kristen Rak, Judith S Bubbear, Moira S Cheung, Signe Sparre Beck-Nielsen, Gabriel T Mindler, Agnès Linglart","doi":"10.1186/s13023-024-03387-4","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":19651,"journal":{"name":"Orphanet Journal of Rare Diseases","volume":"19 Suppl 2","pages":"497"},"PeriodicalIF":3.4000,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11792233/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Orphanet Journal of Rare Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13023-024-03387-4","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}