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Mapping the onset and progression of atrophy in familial frontotemporal lobar degeneration
Background: Frontotemporal lobar degeneration (FTLD) may be inherited as an autosomal dominant disease. Studying patients "at risk" for developing FTLD can provide insights into the earliest onset and evolution of the disease. Method: We carried out approximately annual clinical, MRI, and...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1739516/ https://ncbi.nlm.nih.gov/pubmed/15654025 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.2003.032201 |
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