Julien J - Search Results

1

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: julien j. Ann Neurol. 1999 Aug;46(2):224-33. Ann Neurol. 1999. PMID: 10443888

2

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: julien j. Neurology. 1997 Jul;49(1):133-41. doi: 10.1212/wnl.49.1.133. Neurology. 1997. PMID: 9222181

3

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: julien j. Nat Med. 1997 Sep;3(9):1009-15. doi: 10.1038/nm0997-1009. Nat Med. 1997. PMID: 9288728

4

Analysis of the prion protein gene in thalamic dementia.

Petersen RB, Tabaton M, Berg L, Schrank B, Torack RM, Leal S, Julien J, Vital C, Deleplanque B, Pendlebury WW, et al. Petersen RB, et al. Among authors: julien j. Neurology. 1992 Oct;42(10):1859-63. doi: 10.1212/wnl.42.10.1859. Neurology. 1992. PMID: 1357593 Free PMC article.

5

Widespread dilatation of perivascular spaces: a leukoencephalopathy causing dementia.

Vital C, Julien J. Vital C, et al. Among authors: julien j. Neurology. 1997 May;48(5):1310-3. doi: 10.1212/wnl.48.5.1310. Neurology. 1997. PMID: 9153463

6

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.

Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, Cortelli P, Julien J, Vital C, Pendelbury WW, et al. Goldfarb LG, et al. Among authors: julien j. Science. 1992 Oct 30;258(5083):806-8. doi: 10.1126/science.1439789. Science. 1992. PMID: 1439789

7

Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?

Julien J, Denier C, Ferrer X, Ducros A, Saintarailles J, Lagueny A, Tournier-Lasserve E, Vital C. Julien J, et al. J Neurol. 2001 Mar;248(3):209-14. doi: 10.1007/s004150170228. J Neurol. 2001. PMID: 11355155

8

Peripheral neuropathies and lymphoma without monoclonal gammopathy: a new classification.

Vital C, Vital A, Julien J, Rivel J, deMascarel A, Vergier B, Henry P, Barat M, Reiffers J, Broustet A. Vital C, et al. Among authors: julien j. J Neurol. 1990 Jun;237(3):177-85. doi: 10.1007/BF00314591. J Neurol. 1990. PMID: 2164577 Review.

9

Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I.

Vital A, Vital C, Julien J, Fontan D. Vital A, et al. Among authors: julien j. Acta Neuropathol. 1992;84(4):433-6. doi: 10.1007/BF00227671. Acta Neuropathol. 1992. PMID: 1441924

10

Presence of inclusion body myositis-like filaments in oculopharyngeal muscular dystrophy. Ultrastructural study of 10 cases.

Coquet M, Vital C, Julien J. Coquet M, et al. Among authors: julien j. Neuropathol Appl Neurobiol. 1990 Oct;16(5):393-400. doi: 10.1111/j.1365-2990.1990.tb01275.x. Neuropathol Appl Neurobiol. 1990. PMID: 2175847

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