Adaptive pathway development for Fabry disease: a clinical approach

Author:

Schuller Yvonne,Arends Maarten,Körver Simon,Langeveld Mirjam,Hollak Carla E.M.

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology

Reference49 articles.

1. α-Galactosidase A deficiency: Fabry disease;Desnick,2014

2. Fabry disease: comparison of enzymatic, linkage, and mutation analysis for carrier detection in a family with a novel mutation (30delG);Ashton-Prolla;Am. J. Med. Genet.,1999

3. CNS manifestations of Fabry’s disease;Fellgiebel;Lancet Neurol.,2006

4. Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy;Schiffmann;Nephrol. Dial. Transplant.,2009

5. α-Galactosidase A deficiency: Fabry disease;Desnick,2001

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