Cancel G[au] - Search Results

Year	Number of Results
1980	1
1993	2
1994	4
1995	12
1996	5
1997	7
1998	8
1999	3
2000	1
2001	1
2024	0

1

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I.

Rivaud-Pechoux S, Dürr A, Gaymard B, Cancel G, Ploner CJ, Agid Y, Brice A, Pierrot-Deseilligny C. Rivaud-Pechoux S, et al. Among authors: cancel g. Ann Neurol. 1998 Mar;43(3):297-302. doi: 10.1002/ana.410430306. Ann Neurol. 1998. PMID: 9506545 Review.

2

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: cancel g. Nat Genet. 1995 Oct;11(2):118-9. doi: 10.1038/ng1095-118a. Nat Genet. 1995. PMID: 7550335 No abstract available.

3

Heterogeneous intracellular localization and expression of ataxin-3.

Trottier Y, Cancel G, An-Gourfinkel I, Lutz Y, Weber C, Brice A, Hirsch E, Mandel JL. Trottier Y, et al. Among authors: cancel g. Neurobiol Dis. 1998 Nov;5(5):335-47. doi: 10.1006/nbdi.1998.0208. Neurobiol Dis. 1998. PMID: 10069576

4

Autosomal dominant cerebellar ataxia type I linked to chromosome 12q (SCA2: spinocerebellar ataxia type 2).

Dürr A, Brice A, Lepage-Lezin A, Cancel G, Smadja D, Vernant JC, Agid Y. Dürr A, et al. Among authors: cancel g. Clin Neurosci. 1995;3(1):12-6. Clin Neurosci. 1995. PMID: 7614088 Review.

5

Distribution of ataxin-7 in normal human brain and retina.

Cancel G, Duyckaerts C, Holmberg M, Zander C, Yvert G, Lebre AS, Ruberg M, Faucheux B, Agid Y, Hirsch E, Brice A. Cancel G, et al. Brain. 2000 Dec;123 Pt 12:2519-30. doi: 10.1093/brain/123.12.2519. Brain. 2000. PMID: 11099453

6

Clinical and molecular features of spinocerebellar ataxia type 6.

Stevanin G, Dürr A, David G, Didierjean O, Cancel G, Rivaud S, Tourbah A, Warter JM, Agid Y, Brice A. Stevanin G, et al. Among authors: cancel g. Neurology. 1997 Nov;49(5):1243-6. doi: 10.1212/wnl.49.5.1243. Neurology. 1997. PMID: 9371901

7

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.

David G, Abbas N, Stevanin G, Dürr A, Yvert G, Cancel G, Weber C, Imbert G, Saudou F, Antoniou E, Drabkin H, Gemmill R, Giunti P, Benomar A, Wood N, Ruberg M, Agid Y, Mandel JL, Brice A. David G, et al. Among authors: cancel g. Nat Genet. 1997 Sep;17(1):65-70. doi: 10.1038/ng0997-65. Nat Genet. 1997. PMID: 9288099

8

Differential distribution of the normal and mutated forms of huntingtin in the human brain.

Gourfinkel-An I, Cancel G, Trottier Y, Devys D, Tora L, Lutz Y, Imbert G, Saudou F, Stevanin G, Agid Y, Brice A, Mandel JL, Hirsch EC. Gourfinkel-An I, et al. Among authors: cancel g. Ann Neurol. 1997 Nov;42(5):712-9. doi: 10.1002/ana.410420507. Ann Neurol. 1997. PMID: 9392570

9

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: cancel g. Nature. 1995 Nov 23;378(6555):403-6. doi: 10.1038/378403a0. Nature. 1995. PMID: 7477379

10

Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph disease.

Cancel G, Gourfinkel-An I, Stevanin G, Didierjean O, Abbas N, Hirsch E, Agid Y, Brice A. Cancel G, et al. Hum Mutat. 1998;11(1):23-7. doi: 10.1002/(SICI)1098-1004(1998)11:1<23::AID-HUMU4>3.0.CO;2-M. Hum Mutat. 1998. PMID: 9450899

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