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Cavernomatose cérébrale sporadique révélée par une crise convulsive: à propos d’un cas
Cerebral cavernous malformation is rare. It can occur sporadically or as a familial autosomal dominant disorder (FCCM). It is characterized by the presence of multiple cavernous malformations of the central nervous system. It is often asymptomatic and can be revealed by several symptoms including ce...
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| Publicado no: | Pan Afr Med J |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The African Field Epidemiology Network
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6488239/ https://ncbi.nlm.nih.gov/pubmed/31065320 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2018.31.162.17052 |
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