Stevanin G - Search Results

1

Heterozygous OPA1 mutations in Behr syndrome.

Marelli C, Amati-Bonneau P, Reynier P, Layet V, Layet A, Stevanin G, Brissaud E, Bonneau D, Durr A, Brice A. Marelli C, et al. Among authors: stevanin g. Brain. 2011 Apr;134(Pt 4):e169; author reply e170. doi: 10.1093/brain/awq306. Epub 2010 Nov 26. Brain. 2011. PMID: 21112924 No abstract available.

2

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

3

Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French families.

Khati C, Stevanin G, Durr A, Chneiweiss H, Belal S, Seck A, Cann H, Brice A, Agid Y. Khati C, et al. Among authors: stevanin g. Neurology. 1993 Jun;43(6):1131-7. doi: 10.1212/wnl.43.6.1131. Neurology. 1993. PMID: 8170557

4

Familial essential tremor and idiopathic torsion dystonia are different genetic entities.

Dürr A, Stevanin G, Jedynak CP, Penet C, Agid Y, Brice A. Dürr A, et al. Among authors: stevanin g. Neurology. 1993 Nov;43(11):2212-4. doi: 10.1212/wnl.43.11.2212. Neurology. 1993. PMID: 8232931

5

Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity.

Dürr A, Chneiweiss H, Khati C, Stevanin G, Cancel G, Feingold J, Agid Y, Brice A. Dürr A, et al. Among authors: stevanin g. Brain. 1993 Dec;116 ( Pt 6):1497-508. doi: 10.1093/brain/116.6.1497. Brain. 1993. PMID: 8293283

6

[Does the ataxo-choreic form of DRPLA exist in Europe? Search of mutation in 120 families].

Dubourg O, Dürr A, Chneiweiss H, Stevanin G, Cancel G, Penet C, Agid Y, Brice A. Dubourg O, et al. Among authors: stevanin g. Rev Neurol (Paris). 1995 Nov;151(11):657-60. Rev Neurol (Paris). 1995. PMID: 8745629 French.

7

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. Neurology. 1997 Nov;49(5):1243-6. doi: 10.1212/wnl.49.5.1243. Neurology. 1997. PMID: 9371901

8

Clinical and MRI findings in spinocerebellar ataxia type 5.

Stevanin G, Herman A, Brice A, Dürr A. Stevanin G, et al. Neurology. 1999 Oct 12;53(6):1355-7. doi: 10.1212/wnl.53.6.1355. Neurology. 1999. PMID: 10522902

9

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. Nat Genet. 2000 Mar;24(3):213; author reply 215. doi: 10.1038/73408. Nat Genet. 2000. PMID: 10700167 No abstract available.

10

Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology.

Stevanin G, Dürr A, Brice A. Stevanin G, et al. Eur J Hum Genet. 2000 Jan;8(1):4-18. doi: 10.1038/sj.ejhg.5200403. Eur J Hum Genet. 2000. PMID: 10713882 Review.

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