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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
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 |
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