Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosis

Published:2003-06-11 Issue:1 Volume:28 Page:109-112
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Drory Vivian E.,Birnbaum Miriam,Peleg Leah,Goldman Boleslaw,Korczyn Amos D.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference26 articles.

1. Pure ALS phenotype in a patient with hexosaminidase A deficiency (adult Tay-Sachs disease). Eighth International Symposium on ALS/ MND, Glasgow, UK, 1997.

2. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis

3. The GM2 gangliosidoses. In: editors. The metabolic and molecular basis of inherited disease. New York: McGraw-Hill; 1995. p 2839-2882.

4. Hexosaminidase a activity and amyotrophic lateral sclerosis

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