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MeSH Review

Aphasia, Primary Progressive

 
 
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Gene context of Aphasia, Primary Progressive

  • We present three cases of primary progressive aphasia (PPA) with Pick-variant pathology to support a hypothesis of an underlying nosologic relatedness [5].

References

  1. Clinical and pathological characterization of progressive aphasia. Knibb, J.A., Xuereb, J.H., Patterson, K., Hodges, J.R. Ann. Neurol. (2006) [Pubmed]
  2. Apoe epsilon2-epsilon4 genotype is a possible risk factor for primary progressive aphasia. Acciarri, A., Masullo, C., Bizzarro, A., Valenza, A., Quaranta, D., Marra, C., Tiziano, F.D., Brahe, C., Seripa, D., Matera, M.G., Fazio, V.M., Gainotti, G., Daniele, A. Ann. Neurol. (2006) [Pubmed]
  3. The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia. Kertesz, A., Martinez-Lage, P., Davidson, W., Munoz, D.G. Neurology (2000) [Pubmed]
  4. Progressive dysarthria: definition and clinical follow-up. Soliveri, P., Piacentini, S., Carella, F., Testa, D., Ciano, C., Girotti, F. Neurol. Sci. (2003) [Pubmed]
  5. The pathology and nosology of primary progressive aphasia. Kertesz, A., Hudson, L., Mackenzie, I.R., Munoz, D.G. Neurology (1994) [Pubmed]
 
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