End-stage renal disease in patients with Fabry disease: natural history data from the Fabry Registry | Zendy

Alberto Ortíz | Zendy; Bruno Cianciaruso | Zendy; Marta Cizmarik | Zendy; Dominique P. Germain | Zendy; Renzo Mignani | Zendy; João Paulo Oliveira | Zendy; Jacobo Villalobos | Zendy; Bojan Vujkovac | Zendy; Stephen Waldek | Zendy; Christoph Wanner | Zendy; David G. Warnock | Zendy

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End-stage renal disease in patients with Fabry disease: natural history data from the Fabry Registry

Author(s) -

Alberto Ortíz,

Bruno Cianciaruso,

Marta Cizmarik,

Dominique P. Germain,

Renzo Mignani,

João Paulo Oliveira,

Jacobo Villalobos,

Bojan Vujkovac,

Stephen Waldek,

Christoph Wanner,

David G. Warnock

Publication year - 2009

Publication title -

nephrology dialysis transplantation

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.654

H-Index - 168

eISSN - 1460-2385

pISSN - 0931-0509

DOI - 10.1093/ndt/gfp554

Subject(s) - medicine , fabry disease , natural history , fabry's disease , disease registry , disease , kidney disease

Fabry disease, an X-linked lysosomal storage disorder caused by deficiency of alpha-galactosidase activity, is associated with progressive loss of kidney function. This study was undertaken to characterize Fabry disease among patients who reached end-stage renal disease.

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