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
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014365/
https://www.ncbi.nlm.nih.gov/pubmed/27832731
http://dx.doi.org/10.1080/0886022X.2016.1254656

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014365/
https://www.ncbi.nlm.nih.gov/pubmed/27832731
http://dx.doi.org/10.1080/0886022X.2016.1254656

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