Enzyme replacement therapy in patients with Fabry disease: State of the art and review of the literature-Reference-Cited by-同舟云学术

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Enzyme replacement therapy in patients with Fabry disease: State of the art and review of the literature

Published:2012-11 Issue:3 Volume:107 Page:267-275
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Pisani Antonio,Visciano Bianca,Roux Graciana Diez,Sabbatini Massimo,Porto Caterina,Parenti Giancarlo,Imbriaco Massimo

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference139 articles.

1. High incidence of later-onset Fabry disease revealed by newborn screening;Spada;Am. J. Hum. Genet.,2006

2. Narrative review: Fabry disease;Clarke;Ann. Intern. Med.,2007

3. Fabry's disease;Zarate;Lancet,2008

4. Anderson-Fabry disease: Clinical manifestations and impact of disease in a cohort of 60 obligate carrier females;MacDermot;J. Med. Genet.,2001

5. A 4-year study of the efficacy and tolerability of enzyme replacement therapy with agalsidase alfa in 36 women with Fabry disease;Whybra;Genet. Med.,2009

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1. Fabry disease management: Current status, therapeutic challenges, and future horizons in drug delivery and artificial intelligence assisted diagnosis;Journal of Drug Delivery Science and Technology;2024-10

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