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Creutzfeldt–Jakob disease with unusual presentation of peripheral neuropathy and ophthalmoplegia
Creutzfeldt–Jakob disease (CJD) is a well-described disease. It is characterized by rapidly progressive dementia, myoclonus, ataxia, pyramidal, and extrapyramidal signs. There are well-defined electroencephalogram and magnetic resonance imaging (MRI) findings, and markers found in the cerebrospinal...
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| Publicat a: | Avicenna J Med |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6178565/ https://ncbi.nlm.nih.gov/pubmed/30319957 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ajm.AJM_77_18 |
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