Brice A - Search Results

1

Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.

Lezin A, Cancel G, Stevanin G, Smadja D, Vernant JC, Dürr A, Martial J, Buisson GG, Bellance R, Chneiweiss H, Agid Y, Brice A. Lezin A, et al. Among authors: brice a. Hum Genet. 1996 May;97(5):671-6. doi: 10.1007/BF02281881. Hum Genet. 1996. PMID: 8655151

2

Cardiomyopathy in Friedreich's ataxia: a Doppler-echocardiographic study.

Morvan D, Komajda M, Doan LD, Brice A, Isnard R, Seck A, Lechat P, Agid Y, Grosgogeat Y. Morvan D, et al. Among authors: brice a. Eur Heart J. 1992 Oct;13(10):1393-8. doi: 10.1093/oxfordjournals.eurheartj.a060072. Eur Heart J. 1992. PMID: 1396814

3

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. 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.

4

Choline acetyltransferase activity and [3H]vesamicol binding in the temporal cortex of patients with Alzheimer's disease, Parkinson's disease, and rats with basal forebrain lesions.

Ruberg M, Mayo W, Brice A, Duyckaerts C, Hauw JJ, Simon H, LeMoal M, Agid Y. Ruberg M, et al. Among authors: brice a. Neuroscience. 1990;35(2):327-33. doi: 10.1016/0306-4522(90)90086-j. Neuroscience. 1990. PMID: 2166243

5

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. Among authors: brice a. Am J Hum Genet. 1995 Nov;57(5):1247-50. Am J Hum Genet. 1995. PMID: 7485178 Free PMC article. No abstract available.

6

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

7

Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion.

Gouider R, LeGuern E, Gugenheim M, Tardieu S, Maisonobe T, Léger JM, Vallat JM, Agid Y, Bouche P, Brice A. Gouider R, et al. Among authors: brice a. Neurology. 1995 Nov;45(11):2018-23. doi: 10.1212/wnl.45.11.2018. Neurology. 1995. PMID: 7501152

8

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

9

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: brice a. Clin Neurosci. 1995;3(1):12-6. Clin Neurosci. 1995. PMID: 7614088 Review.

10

Sequence analysis of the CCG polymorphic region adjacent to the CAG triplet repeat of the HD gene in normal and HD chromosomes.

Pêcheux C, Mouret JF, Dürr A, Agid Y, Feingold J, Brice A, Dodé C, Kaplan JC. Pêcheux C, et al. Among authors: brice a. J Med Genet. 1995 May;32(5):399-400. doi: 10.1136/jmg.32.5.399. J Med Genet. 1995. PMID: 7616551 Free PMC article.

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