Brice A - Search Results

1

Are (CTG)n expansions at the SCA8 locus rare polymorphisms?

Stevanin G, Herman A, Dürr A, Jodice C, Frontali M, Agid Y, Brice A. Stevanin G, et al. Among authors: brice a. Nat Genet. 2000 Mar;24(3):213; author reply 215. doi: 10.1038/73408. Nat Genet. 2000. PMID: 10700167 No abstract available.

2

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: brice a. Nat Genet. 1997 Sep;17(1):65-70. doi: 10.1038/ng0997-65. Nat Genet. 1997. PMID: 9288099

3

SCA2 is not a major locus for ADCA type I in French families.

Cancel G, Stevanin G, Dürr A, Chneiweiss H, Penet C, Pothin Y, Agid Y, Brice A. Cancel G, et al. Among authors: brice a. Am J Med Genet. 1995 Oct 9;60(5):382-5. doi: 10.1002/ajmg.1320600507. Am J Med Genet. 1995. PMID: 8546150

4

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.

Gispert S, Twells R, Orozco G, Brice A, Weber J, Heredero L, Scheufler K, Riley B, Allotey R, Nothers C, et al. Gispert S, et al. Among authors: brice a. Nat Genet. 1993 Jul;4(3):295-9. doi: 10.1038/ng0793-295. Nat Genet. 1993. PMID: 8358438

5

Linkage disequilibrium at the SCA2 locus.

Didierjean O, Cancel G, Stevanin G, Dürr A, Bürk K, Benomar A, Lezin A, Belal S, Abada-Bendid M, Klockgether T, Brice A. Didierjean O, et al. Among authors: brice a. J Med Genet. 1999 May;36(5):415-7. J Med Genet. 1999. PMID: 10353790 Free PMC article.

6

A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.

Holmes SE, O'Hearn E, Rosenblatt A, Callahan C, Hwang HS, Ingersoll-Ashworth RG, Fleisher A, Stevanin G, Brice A, Potter NT, Ross CA, Margolis RL. Holmes SE, et al. Among authors: brice a. Nat Genet. 2001 Dec;29(4):377-8. doi: 10.1038/ng760. Nat Genet. 2001. PMID: 11694876

7

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.

Imbert G, Saudou F, Yvert G, Devys D, Trottier Y, Garnier JM, Weber C, Mandel JL, Cancel G, Abbas N, Dürr A, Didierjean O, Stevanin G, Agid Y, Brice A. Imbert G, et al. Among authors: brice a. Nat Genet. 1996 Nov;14(3):285-91. doi: 10.1038/ng1196-285. Nat Genet. 1996. PMID: 8896557

8

Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study Group.

Brice A, Tardieu S, Campion D, Le Guern E, Martinez M, Carpentier A, Penet C, Dubois B, Bellis M, Mallet J, et al. Brice A, et al. Am J Med Genet. 1995 Apr 24;60(2):91-3. doi: 10.1002/ajmg.1320600202. Am J Med Genet. 1995. PMID: 7485257

9

CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients.

Stevanin G, Camuzat A, Holmes SE, Julien C, Sahloul R, Dodé C, Hahn-Barma V, Ross CA, Margolis RL, Durr A, Brice A. Stevanin G, et al. Among authors: brice a. Neurology. 2002 Mar 26;58(6):965-7. doi: 10.1212/wnl.58.6.965. Neurology. 2002. PMID: 11914418

10

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, Brice A, LeGuern E, Moulard B, Chaigne D, Buresi C, Malafosse A. Escayg A, et al. Among authors: brice a. Nat Genet. 2000 Apr;24(4):343-5. doi: 10.1038/74159. Nat Genet. 2000. PMID: 10742094 No abstract available.

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