Brice A - Search Results

1

Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?

Tassin J, Dürr A, Bonnet AM, Gil R, Vidailhet M, Lücking CB, Goas JY, Durif F, Abada M, Echenne B, Motte J, Lagueny A, Lacomblez L, Jedynak P, Bartholomé B, Agid Y, Brice A. Tassin J, et al. Among authors: brice a. Brain. 2000 Jun;123 ( Pt 6):1112-21. doi: 10.1093/brain/123.6.1112. Brain. 2000. PMID: 10825351

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

Decreased choline acetyltransferase mRNA expression in the nucleus basalis of Meynert in Alzheimer disease: an in situ hybridization study.

Strada O, Vyas S, Hirsch EC, Ruberg M, Brice A, Agid Y, Javoy-Agid F. Strada O, et al. Among authors: brice a. Proc Natl Acad Sci U S A. 1992 Oct 15;89(20):9549-53. doi: 10.1073/pnas.89.20.9549. Proc Natl Acad Sci U S A. 1992. PMID: 1409664 Free PMC article.

4

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.

5

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

6

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

7

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.

8

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.

9

Diagnosis of "sporadic" Huntington's disease.

Dürr A, Dodé C, Hahn V, Pêcheux C, Pillon B, Feingold J, Kaplan JC, Agid Y, Brice A. Dürr A, et al. Among authors: brice a. J Neurol Sci. 1995 Mar;129(1):51-5. doi: 10.1016/0022-510x(94)00250-r. J Neurol Sci. 1995. PMID: 7751845

10

[Cerebellar ataxia with autosomal dominant transmission].

Dürr A, Brice A. Dürr A, et al. Among authors: brice a. Rev Neurol (Paris). 1994 Oct;150(10):661-3. Rev Neurol (Paris). 1994. PMID: 7792472 French. No abstract available.

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