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Electroneuromyographic Features in Fabry Disease: A Retrospective Review
INTRODUCTION: Fabry disease (FD) is an X-linked recessive inherited disorder characterized by lysosomal alpha-galactosidase deficiency. The purpose of our study was to assess and compare the electroneuromyographic (ENMG) findings of 15 patients with Fabry disease and the electroneurographic (ENG) fi...
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| Publicat a: | Noro Psikiyatr Ars |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Turkish Neuropsychiatric Society
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5353058/ https://ncbi.nlm.nih.gov/pubmed/28360720 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/npa.2015.7646 |
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