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Vestibular and Saccadic Abnormalities in Gaucher’s Disease

Gaucher’s disease (GD) is a hereditary lysosomal storage disease characterized by abnormal deposition of glucocerebroside due to the enzyme glucocerebrosidase deficiency, resulting in multi-organ pathology. GD type III has a progressive neurological involvement. We studied the vestibular and saccadi...

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Autors principals: Chen, Luke, Halmagyi, G. Michael, Todd, Michael J., Aw, Swee T.
Format: Artigo
Idioma:Inglês
Publicat: Springer Berlin Heidelberg 2013
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4110333/
https://ncbi.nlm.nih.gov/pubmed/24142279
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2013_264
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