Lemieux B - Search Results

1

Phenotypic Manifestations in French-Canadian Population with Charcot-Marie-Tooth Disease Type 1A Associated with 17p11.2 Duplication.

Dupré N, Bouchard JP, Cossette L, Brunet D, Vanasse M, Lemieux B, Mathon G, Puymirat J. Dupré N, et al. Among authors: lemieux b. Ann N Y Acad Sci. 1999 Oct;883(1):497-499. doi: 10.1111/j.1749-6632.1999.tb08620.x. Ann N Y Acad Sci. 1999. PMID: 29086976 No abstract available.

2

Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplication.

Dupré N, Bouchard JP, Cossette L, Brunet D, Vanasse M, Lemieux B, Mathon G, Puymirat J. Dupré N, et al. Among authors: lemieux b. Can J Neurol Sci. 1999 Aug;26(3):196-200. doi: 10.1017/s031716710000024x. Can J Neurol Sci. 1999. PMID: 10451742

3

Phenotypic manifestations in French-Canadian populations with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication.

Dupré N, Bouchard JP, Cossette L, Brunet D, Vanasse M, Lemieux B, Mathon G, Puymirat J. Dupré N, et al. Among authors: lemieux b. Ann N Y Acad Sci. 1999 Sep 14;883:497-9. Ann N Y Acad Sci. 1999. PMID: 10586283 No abstract available.

4

Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion.

Montermini L, Richter A, Morgan K, Justice CM, Julien D, Castellotti B, Mercier J, Poirier J, Capozzoli F, Bouchard JP, Lemieux B, Mathieu J, Vanasse M, Seni MH, Graham G, Andermann F, Andermann E, Melançon SB, Keats BJ, Di Donato S, Pandolfo M. Montermini L, et al. Among authors: lemieux b. Ann Neurol. 1997 May;41(5):675-82. doi: 10.1002/ana.410410518. Ann Neurol. 1997. PMID: 9153531

5

Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian families.

Simard LR, Vanasse M, Rochette C, Morgan K, Lemieux B, Melançon SB, Labuda D. Simard LR, et al. Among authors: lemieux b. Genomics. 1992 Sep;14(1):188-90. doi: 10.1016/s0888-7543(05)80305-2. Genomics. 1992. PMID: 1427826

6

Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian population.

Simard LR, Prescott G, Rochette C, Morgan K, Lemieux B, Mathieu J, Melançon SB, Vanasse M. Simard LR, et al. Among authors: lemieux b. Hum Mol Genet. 1994 Mar;3(3):459-63. doi: 10.1093/hmg/3.3.459. Hum Mol Genet. 1994. PMID: 8012358

7

Human myoblast transplantation: preliminary results of 4 cases.

Huard J, Bouchard JP, Roy R, Malouin F, Dansereau G, Labrecque C, Albert N, Richards CL, Lemieux B, Tremblay JP. Huard J, et al. Among authors: lemieux b. Muscle Nerve. 1992 May;15(5):550-60. doi: 10.1002/mus.880150504. Muscle Nerve. 1992. PMID: 1584246

8

Origin of Friedreich's disease in Quebec.

Barbeau A, Sadibelouiz M, Roy M, Lemieux B, Bouchard JP, Geoffroy G. Barbeau A, et al. Among authors: lemieux b. Can J Neurol Sci. 1984 Nov;11(4 Suppl):506-9. doi: 10.1017/s0317167100034971. Can J Neurol Sci. 1984. PMID: 6391645

9

Myoblast transplantation produced dystrophin-positive muscle fibres in a 16-year-old patient with Duchenne muscular dystrophy.

Huard J, Bouchard JP, Roy R, Labrecque C, Dansereau G, Lemieux B, Tremblay JP. Huard J, et al. Among authors: lemieux b. Clin Sci (Lond). 1991 Aug;81(2):287-8. doi: 10.1042/cs0810287. Clin Sci (Lond). 1991. PMID: 1653675 No abstract available.

10

Nerve conduction studies and electromyography in Friedreich's ataxia.

Peyronnard JM, Lapointe L, Bouchard JP, Lamontagne A, Lemieux B, Barbeau A. Peyronnard JM, et al. Among authors: lemieux b. Can J Neurol Sci. 1976 Nov;3(4):313-7. doi: 10.1017/s0317167100025518. Can J Neurol Sci. 1976. PMID: 1000415

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