Enzyme replacement therapy in the mouse model of Pompe disease-Reference-Cited by-同舟云学术

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Enzyme replacement therapy in the mouse model of Pompe disease

Published:2003-09 Issue:1-2 Volume:80 Page:159-169
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Raben N,Danon M,Gilbert A.L,Dwivedi S,Collins B,Thurberg B.L,Mattaliano R.J,Nagaraju K,Plotz P.H

Publisher

Elsevier BV

Subject

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

Reference50 articles.

1. Replacement therapy for inherited enzyme deficiency – macrophage-targeted glucocerebrosidase for Gaucher’s disease;Barton;N. Engl. J. Med.,1991

2. Enzyme replacement and enhancement therapies: lessons from lysosomal disorders;Desnick;Nat. Rev. Genet.,2002

3. Enzyme replacement therapy for the mucopolysaccharide storage disorders;Kakkis;Expert. Opin. Investig. Drugs,2002

4. Enzyme therapy for Pompe disease: from science to industrial enterprise;Reuser;Eur. J. Pediatr.,2002

5. Alpha-glucosidase deficiency in generalize glycogen storage disease (Pompe’s disease);Hers;Biochem. J.,1963

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3. Diaphragm weakness in late-onset Pompe disease: A complex interplay between lower motor neuron and muscle fibre degeneration;Journal of the Neurological Sciences;2024-05

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