Gastrointestinal involvement in Fabry disease. So important, yet often neglected-Reference-Cited by-同舟云学术

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Gastrointestinal involvement in Fabry disease. So important, yet often neglected

Published:2015-09-29 Issue:1 Volume:89 Page:5-9
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Politei J.¹,Thurberg B.L.²,Wallace E.³,Warnock D.³,Serebrinsky G.⁴,Durand C.¹,Schenone A.B.¹

Affiliation:

1. Department of Neurology; Fundación para el Estudio de las Enfermedades Neurometabólicas (FESEN); Buenos Aires Argentina

2. Department of Pathology; Genzyme Corporation; Framingham MA USA

3. Department of Medicine; University of Alabama; Birmingham AL USA

4. Department of Genetics; LABGEN; Buenos Aires Argentina

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.12673/fullpdf

Reference33 articles.

1. Fabry disease;Germain;Orphanet J Rare Dis,2010

2. α-Galactosidase A knockout mice: progressive organ pathology resembles the type 2 later-onset phenotype of Fabry disease;Bangari;Am J Pathol,2015

3. Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy;Thurberg;Kidney Int,2002

4. Monitoring the 3-year efficacy of enzyme replacement therapy in fabry disease by repeated skin biopsies;Thurberg;J Invest Dermatol,2004

5. Cardiac microvascular pathology in Fabry disease: evaluation of endomyocardial biopsies before and after enzyme replacement therapy;Thurberg;Circulation,2009

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