Urine Bikunin as a Marker of Renal Impairment in Fabry's Disease

Fabry's disease is a rare lysosomal storage disorder caused by the deficiency of α-galactosidase A that leads to the accumulation of neutral glycosphingolipids in many organs including kidney, heart, and brain. Since end-stage renal disease represents a major complication of this pathology, the...

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Detalles Bibliográficos
Autores principales: Lepedda, Antonio Junior, Fancellu, Laura, Zinellu, Elisabetta, De Muro, Pierina, Nieddu, Gabriele, Deiana, Giovanni Andrea, Canu, Piera, Concolino, Daniela, Sestito, Simona, Formato, Marilena, Sechi, Gianpietro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694371/
https://www.ncbi.nlm.nih.gov/pubmed/23841057
http://dx.doi.org/10.1155/2013/205948

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694371/
https://www.ncbi.nlm.nih.gov/pubmed/23841057
http://dx.doi.org/10.1155/2013/205948

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