Robitaille Y - Search Results

1

Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.

Lopes-Cendes I, Maciel P, Kish S, Gaspar C, Robitaille Y, Clark HB, Koeppen AH, Nance M, Schut L, Silveira I, Coutinho P, Sequeiros J, Rouleau GA. Lopes-Cendes I, et al. Among authors: robitaille y. Ann Neurol. 1996 Aug;40(2):199-206. doi: 10.1002/ana.410400211. Ann Neurol. 1996. PMID: 8773601

2

Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype.

Robitaille Y, Schut L, Kish SJ. Robitaille Y, et al. Acta Neuropathol. 1995;90(6):572-81. doi: 10.1007/BF00318569. Acta Neuropathol. 1995. PMID: 8615077

3

Limits of clinical assessment in the accurate diagnosis of Machado-Joseph disease.

Lopes-Cendes I, Silveira I, Maciel P, Gaspar C, Radvany J, Chitayat D, Babul R, Stewart J, Dolliver M, Robitaille Y, Rouleau GA, Sequeiros J. Lopes-Cendes I, et al. Among authors: robitaille y. Arch Neurol. 1996 Nov;53(11):1168-74. doi: 10.1001/archneur.1996.00550110120020. Arch Neurol. 1996. PMID: 8912491

4

The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.

Robitaille Y, Lopes-Cendes I, Becher M, Rouleau G, Clark AW. Robitaille Y, et al. Brain Pathol. 1997 Jul;7(3):901-26. doi: 10.1111/j.1750-3639.1997.tb00893.x. Brain Pathol. 1997. PMID: 9217975 Free PMC article. Review.

5

Brain amino acid reductions in one family with chromosome 6p-linked dominantly inherited olivopontocerebellar atrophy.

Kish SJ, Robitaille Y, el-Awar M, Gilbert J, Deck J, Chang LJ, Schut L. Kish SJ, et al. Among authors: robitaille y. Ann Neurol. 1991 Dec;30(6):780-4. doi: 10.1002/ana.410300606. Ann Neurol. 1991. PMID: 1686387

6

Quinolinic acid catabolism is increased in cerebellum of patients with dominantly inherited olivopontocerebellar atrophy.

Kish SJ, Du F, Parks DA, Robitaille Y, Ball MJ, Schut L, Hornykiewicz O, Schwarcz R. Kish SJ, et al. Among authors: robitaille y. Ann Neurol. 1991 Jan;29(1):100-4. doi: 10.1002/ana.410290119. Ann Neurol. 1991. PMID: 1825460

7

Non-Alzheimer-type pattern of brain cholineacetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy.

Kish SJ, Robitaille Y, el-Awar M, Deck JH, Simmons J, Schut L, Chang LJ, DiStefano L, Freedman M. Kish SJ, et al. Among authors: robitaille y. Ann Neurol. 1989 Sep;26(3):362-7. doi: 10.1002/ana.410260309. Ann Neurol. 1989. PMID: 2802535

8

Striatal dopamine nerve terminal markers but not nigral cellularity are reduced in spinocerebellar ataxia type 1.

Kish SJ, Guttman M, Robitaille Y, el-Awar M, Chang LJ, Levey AI. Kish SJ, et al. Among authors: robitaille y. Neurology. 1997 Apr;48(4):1109-11. doi: 10.1212/wnl.48.4.1109. Neurology. 1997. PMID: 9109912

9

Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: an MRI volumetric study.

Cendes F, Andermann F, Dubeau F, Gloor P, Evans A, Jones-Gotman M, Olivier A, Andermann E, Robitaille Y, Lopes-Cendes I, et al. Cendes F, et al. Among authors: robitaille y. Neurology. 1993 Jun;43(6):1083-7. doi: 10.1212/wnl.43.6.1083. Neurology. 1993. PMID: 8170546

10

Atrophy of mesial structures in patients with temporal lobe epilepsy: cause or consequence of repeated seizures?

Cendes F, Andermann F, Gloor P, Lopes-Cendes I, Andermann E, Melanson D, Jones-Gotman M, Robitaille Y, Evans A, Peters T. Cendes F, et al. Among authors: robitaille y. Ann Neurol. 1993 Dec;34(6):795-801. doi: 10.1002/ana.410340607. Ann Neurol. 1993. PMID: 8250528

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