Durr A - Search Results

1

Large pathogenic expansions in the SCA2 and SCA7 genes can be detected by fluorescent repeat-primed polymerase chain reaction assay.

Cagnoli C, Stevanin G, Michielotto C, Gerbino Promis G, Brussino A, Pappi P, Durr A, Dragone E, Viemont M, Gellera C, Brice A, Migone N, Brusco A. Cagnoli C, et al. Among authors: durr a. J Mol Diagn. 2006 Feb;8(1):128-32. doi: 10.2353/jmoldx.2006.050043. J Mol Diagn. 2006. PMID: 16436644 Free PMC article.

2

[Cerebellar ataxia with autosomal dominant transmission].

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

3

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: durr a. Ann Neurol. 1995 Feb;37(2):176-80. doi: 10.1002/ana.410370207. Ann Neurol. 1995. PMID: 7847859

4

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: durr a. Am J Med Genet. 1995 Oct 9;60(5):382-5. doi: 10.1002/ajmg.1320600507. Am J Med Genet. 1995. PMID: 8546150

5

Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph disease.

Stevanin G, Cassa E, Cancel G, Abbas N, Dürr A, Jardim E, Agid Y, Sousa PS, Brice A. Stevanin G, et al. Among authors: durr a. J Med Genet. 1995 Oct;32(10):827-30. doi: 10.1136/jmg.32.10.827. J Med Genet. 1995. PMID: 8558567 Free PMC article.

6

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.

Dürr A, Stevanin G, Cancel G, Duyckaerts C, Abbas N, Didierjean O, Chneiweiss H, Benomar A, Lyon-Caen O, Julien J, Serdaru M, Penet C, Agid Y, Brice A. Dürr A, et al. Ann Neurol. 1996 Apr;39(4):490-9. doi: 10.1002/ana.410390411. Ann Neurol. 1996. PMID: 8619527

7

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: durr a. Hum Genet. 1996 May;97(5):671-6. doi: 10.1007/BF02281881. Hum Genet. 1996. PMID: 8655151

8

[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: durr a. Rev Neurol (Paris). 1995 Nov;151(11):657-60. Rev Neurol (Paris). 1995. PMID: 8745629 French.

9

Genetics of movement disorders.

Dürr A, Brice A. Dürr A, et al. Curr Opin Neurol. 1996 Aug;9(4):290-7. doi: 10.1097/00019052-199608000-00009. Curr Opin Neurol. 1996. PMID: 8858187 Review.

10

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: durr a. Nat Genet. 1996 Nov;14(3):285-91. doi: 10.1038/ng1196-285. Nat Genet. 1996. PMID: 8896557

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