Enzyme therapy for Pompe disease with recombinant human α-glucosidase from rabbit milk-Reference-Cited by-同舟云学术

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Enzyme therapy for Pompe disease with recombinant human α-glucosidase from rabbit milk

Published:2001-04 Issue:2 Volume:24 Page:266-274
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Van den Hout J. M. P.¹,Reuser A. J. J.²,de Klerk J. B. C.¹,Arts W. F.³,Smeitink J. A. M.¹,Van der Ploeg A. T.¹

Affiliation:

1. ; Department of Pediatrics, Division of Metabolic Diseases; Sophia Children's Hospital, University Hospital Rotterdam; The Netherlands

2. ; Department of Clinical Genetics; Erasmus University Rotterdam; The Netherlands

3. ; Department of Child Neurology, Sophia Children's Hospital; University Hospital Rotterdam; The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1010383421286/fullpdf

Reference16 articles.

1. An electron microscopic and biochemical study of type II glycogenosis;Baudhuin;Lab Invest,1964

2. Recombinant human acid a-glucosidase: high level production in mouse milk, biochemical characteristics, correction of enzyme de¢ciency in GSDII KO mice;Bijvoet;Hum Mol Genet,1998

3. Enzyme replacement in Pompe dis-ease: an attempt with puri¢ed human acid a-glucosidase;De Barsy;Birth Defects,1973

4. Glycogen storage disease of the myocardium with obstruction to left ventricular out£ow;Ehlers;Circulation,1962

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