Screening Fabry’s disease in chronic kidney disease patients not on dialysis: a multicenter study

Objectives: Fabry's disease is an X-linked inherited, rare, progressive, lysosomal storage disorder, affecting multiple organs due to the deficient activity of α-galactosidase A (α-Gal A) enzyme. The prevalence has been reported to be 0.15–1% in hemodialysis patients; however, the information o...

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Detalles Bibliográficos
Publicado en:Ren Fail
Main Authors: Yeniçerioğlu, Yavuz, Akdam, Hakan, Dursun, Belda, Alp, Alper, Sağlam Eyiler, Funda, Akın, Davut, Gün, Yelda, Hüddam, Bülent, Batmazoğlu, Mehmet, Gibyeli Genek, Dilek, Pirinççi, Serhat, Ersoy, İsmail Rıfkı, Üzüm, Atilla, Soypaçacı, Zeki, Tanrısev, Mehmet, Çolak, Hülya, Demiral Sezer, Sibel, Bozkurt, Gökay, Akyıldız, Utku Oğan, Akyüz Ünsal, Ayşe İpek, Ünübol, Mustafa, Uslu, Meltem, Eryılmaz, Ufuk, Günel, Ceren, Meteoğlu, İbrahim, Yavaşoğlu, İrfan, Ünsal, Alparslan, Akar, Harun, Okyay, Pınar
Formato: Artigo
Idioma:Inglês
Publicado: Taylor & Francis 2016
Assuntos:
Clinical Study
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6014365/
https://ncbi.nlm.nih.gov/pubmed/27832731
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/0886022X.2016.1254656
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