The International X-Linked Hypophosphatemia (XLH) Registry: first interim analysis of baseline demographic, genetic and clinical data.

Autor: Ariceta, Gema1 (AUTHOR) gema.ariceta@vallhebron.cat, Beck-Nielsen, Signe Sparre2,3 (AUTHOR), Boot, Annemieke M.4 (AUTHOR), Brandi, Maria Luisa5,6 (AUTHOR), Briot, Karine7 (AUTHOR), de Lucas Collantes, Carmen8,9 (AUTHOR), Emma, Francesco10 (AUTHOR), Giannini, Sandro11 (AUTHOR), Haffner, Dieter12 (AUTHOR), Keen, Richard13 (AUTHOR), Levtchenko, Elena14 (AUTHOR), Mӓkitie, Outi15 (AUTHOR), Mughal, M. Zulf16 (AUTHOR), Nilsson, Ola17,18 (AUTHOR), Schnabel, Dirk19 (AUTHOR), Tripto-Shkolnik, Liana20,21 (AUTHOR), Liu, Jonathan22 (AUTHOR), Williams, Angela22 (AUTHOR), Wood, Sue22 (AUTHOR), Zillikens, M. Carola23 (AUTHOR)
Zdroj: Orphanet Journal of Rare Diseases. 10/21/2023, Vol. 18 Issue 1, p1-17. 17p.
Databáze: Academic Search Ultimate
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