NEUROLOGICAL ASSESSMENT OF EGYPTIAN PATIENTS WITH GAUCHER DISEASE
AL SHAIMAA ADEL MOHAMMED EL-KHATIB;
Abstract
G
aucher disease (GD), the most common lysosomal storage disease, is an autosomal recessive, multi-systemic glycosphingolipid disorder.
Three phenotypes have been identified.
Most patients of G.D express the chronic non neuropathic form type I, they ar
aucher disease (GD), the most common lysosomal storage disease, is an autosomal recessive, multi-systemic glycosphingolipid disorder.
Three phenotypes have been identified.
Most patients of G.D express the chronic non neuropathic form type I, they ar
Other data
| Title | NEUROLOGICAL ASSESSMENT OF EGYPTIAN PATIENTS WITH GAUCHER DISEASE | Other Titles | دراسة لتقييم تأثير مرض جوشر من الناحية العصبية على المرضى من الأطفال المصريين | Authors | AL SHAIMAA ADEL MOHAMMED EL-KHATIB | Keywords | NEUROLOGICAL ASSESSMENT OF EGYPTIAN PATIENTS WITH GAUCHER DISEASE | Issue Date | 2010 | Description | G aucher disease (GD), the most common lysosomal storage disease, is an autosomal recessive, multi-systemic glycosphingolipid disorder. Three phenotypes have been identified. Most patients of G.D express the chronic non neuropathic form type I, they ar |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 92380444.pdf | 278.1 kB | Adobe PDF | View/Open |
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