Stevanin G - Search Results

1

Cancel G, Dürr A, Stevanin G, Chneiweiss H, Duyckaerts C, Serdaru M, de Toffol B, Agid Y, Brice A. Cancel G, et al. Among authors: stevanin g. Nat Genet. 1994 Jan;6(1):8. doi: 10.1038/ng0194-8. Nat Genet. 1994. PMID: 8136838 No abstract available.

2

Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.

Brice A, Ravisé N, Stevanin G, Gugenheim M, Bouche P, Penet C, Agid Y. Brice A, et al. Among authors: stevanin g. J Med Genet. 1992 Nov;29(11):807-12. doi: 10.1136/jmg.29.11.807. J Med Genet. 1992. PMID: 1453432 Free PMC article.

3

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias.

Trottier Y, Lutz Y, Stevanin G, Imbert G, Devys D, Cancel G, Saudou F, Weber C, David G, Tora L, et al. Trottier Y, et al. Among authors: stevanin g. Nature. 1995 Nov 23;378(6555):403-6. doi: 10.1038/378403a0. Nature. 1995. PMID: 7477379

4

Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutation.

Stevanin G, Cancel G, Didierjean O, Dürr A, Abbas N, Cassa E, Feingold J, Agid Y, Brice A. Stevanin G, et al. Am J Hum Genet. 1995 Nov;57(5):1247-50. Am J Hum Genet. 1995. PMID: 7485178 Free PMC article. No abstract available.

5

Gender equality in Machado-Joseph disease.

Dürr A, Stevanin G, Cancel G, Abbas N, Chneiweiss H, Agid Y, Feingold J, Brice A. Dürr A, et al. Among authors: stevanin g. Nat Genet. 1995 Oct;11(2):118-9. doi: 10.1038/ng1095-118a. Nat Genet. 1995. PMID: 7550335 No abstract available.

6

Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.

Cancel G, Abbas N, Stevanin G, Dürr A, Chneiweiss H, Néri C, Duyckaerts C, Penet C, Cann HM, Agid Y, et al. Cancel G, et al. Among authors: stevanin g. Am J Hum Genet. 1995 Oct;57(4):809-16. Am J Hum Genet. 1995. PMID: 7573040 Free PMC article.

7

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.

Benomar A, Krols L, Stevanin G, Cancel G, LeGuern E, David G, Ouhabi H, Martin JJ, Dürr A, Zaim A, et al. Benomar A, et al. Among authors: stevanin g. Nat Genet. 1995 May;10(1):84-8. doi: 10.1038/ng0595-84. Nat Genet. 1995. PMID: 7647798

8

Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia.

Fontaine B, Rime CS, Hazan J, Dürr A, Stevanin G, Penet C, Reboul J, Agid Y, Lyon-Caen O, Baumann N, et al. Fontaine B, et al. Among authors: stevanin g. Neuromuscul Disord. 1995 Jan;5(1):11-7. doi: 10.1016/0960-8966(94)e0024-3. Neuromuscul Disord. 1995. PMID: 7719135

9

The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.

Stevanin G, Cancel G, Dürr A, Chneiweiss H, Dubourg O, Weissenbach J, Cann HM, Agid Y, Brice A. Stevanin G, et al. Am J Hum Genet. 1995 Jan;56(1):193-201. Am J Hum Genet. 1995. PMID: 7825578 Free PMC article.

10

Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia: clinical and molecular correlations.

Dubourg O, Dürr A, Cancel G, Stevanin G, Chneiweiss H, Penet C, Agid Y, Brice A. Dubourg O, et al. Among authors: stevanin g. Ann Neurol. 1995 Feb;37(2):176-80. doi: 10.1002/ana.410370207. Ann Neurol. 1995. PMID: 7847859

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