Vital C - Search Results

1

Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case.

Ghorayeb I, Series C, Parchi P, Sawan B, Guez S, Laplanche JL, Capellari S, Gambetti P, Vital C. Ghorayeb I, et al. Among authors: vital c. Neurology. 1998 Jul;51(1):271-4. doi: 10.1212/wnl.51.1.271. Neurology. 1998. PMID: 9674819

2

Pathologic prion protein spreading in the peripheral nervous system of a patient with sporadic Creutzfeldt-Jakob disease.

Favereaux A, Quadrio I, Vital C, Perret-Liaudet A, Anne O, Laplanche JL, Petry KG, Vital A. Favereaux A, et al. Among authors: vital a, vital c. Arch Neurol. 2004 May;61(5):747-50. doi: 10.1001/archneur.61.5.747. Arch Neurol. 2004. PMID: 15148153

3

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, Ghetti B, Gambetti P, Kretzschmar H. Parchi P, et al. Among authors: vital c. Ann Neurol. 1999 Aug;46(2):224-33. Ann Neurol. 1999. PMID: 10443888

4

A French cluster of Creutzfeldt-Jakob disease: a molecular analysis.

Beaudry P, Parchi P, Peoc'h K, Desbordes P, Dartigues JF, Vital A, Vital C, Capellari S, Gambetti P, Delasnerie-Lauprêtre N, Mary JY, Laplanche JL. Beaudry P, et al. Among authors: vital a, vital c. Eur J Neurol. 2002 Sep;9(5):457-62. doi: 10.1046/j.1468-1331.2002.00456.x. Eur J Neurol. 2002. PMID: 12220376

5

Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

Capellari S, Vital C, Parchi P, Petersen RB, Ferrer X, Jarnier D, Pegoraro E, Gambetti P, Julien J. Capellari S, et al. Among authors: vital c. Neurology. 1997 Jul;49(1):133-41. doi: 10.1212/wnl.49.1.133. Neurology. 1997. PMID: 9222181

6

Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits.

Vital C, Gray F, Vital A, Parchi P, Capellari S, Petersen RB, Ferrer X, Jarnier D, Julien J, Gambetti P. Vital C, et al. Among authors: vital a. Neuropathol Appl Neurobiol. 1998 Apr;24(2):125-30. doi: 10.1046/j.1365-2990.1998.00098.x. Neuropathol Appl Neurobiol. 1998. PMID: 9634208 Review.

7

The nigrostriatal pathway in Creutzfeldt-Jakob disease.

Vital A, Fernagut PO, Canron MH, Joux J, Bezard E, Martin-Negrier ML, Vital C, Tison F. Vital A, et al. Among authors: vital c. J Neuropathol Exp Neurol. 2009 Jul;68(7):809-15. doi: 10.1097/NEN.0b013e3181abdae8. J Neuropathol Exp Neurol. 2009. PMID: 19535991

8

Allelic origin of the abnormal prion protein isoform in familial prion diseases.

Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P. Chen SG, et al. Among authors: vital c. Nat Med. 1997 Sep;3(9):1009-15. doi: 10.1038/nm0997-1009. Nat Med. 1997. PMID: 9288728

9

Neuronal apoptosis in fatal familial insomnia.

Dorandeu A, Wingertsmann L, Chrétien F, Delisle MB, Vital C, Parchi P, Montagna P, Lugaresi E, Ironside JW, Budka H, Gambetti P, Gray F. Dorandeu A, et al. Among authors: vital c. Brain Pathol. 1998 Jul;8(3):531-7. doi: 10.1111/j.1750-3639.1998.tb00175.x. Brain Pathol. 1998. PMID: 9669704 Free PMC article.

10

Corneal myxoma associated with keratoconus and Down's syndrome.

Léger F, Sawan B, Mortemousque B, Williamson W, Vital C. Léger F, et al. Among authors: vital c. Cornea. 2000 Jul;19(4):561-3. doi: 10.1097/00003226-200007000-00032. Cornea. 2000. PMID: 10928779

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