Dürr A - Search Results

1

FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.

Biancalana V, Toft M, Le Ber I, Tison F, Scherrer E, Thibodeau S, Mandel JL, Brice A, Farrer MJ, Dürr A. Biancalana V, et al. Among authors: durr a. Arch Neurol. 2005 Jun;62(6):962-6. doi: 10.1001/archneur.62.6.962. Arch Neurol. 2005. PMID: 15956167

2

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

3

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: durr 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.

4

[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.

5

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

6

The phenotype of "pure" autosomal dominant spastic paraplegia.

Dürr A, Brice A, Serdaru M, Rancurel G, Derouesné C, Lyon-Caen O, Agid Y, Fontaine B. Dürr A, et al. Neurology. 1994 Jul;44(7):1274-7. doi: 10.1212/wnl.44.7.1274. Neurology. 1994. PMID: 8035929

7

Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.

Benomar A, Le Guern E, Dürr A, Ouhabi H, Stevanin G, Yahyaoui M, Chkili T, Agid Y, Brice A. Benomar A, et al. Among authors: durr a. Ann Neurol. 1994 Apr;35(4):439-44. doi: 10.1002/ana.410350411. Ann Neurol. 1994. PMID: 8154871

8

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: durr a. Neurology. 1993 Jun;43(6):1131-7. doi: 10.1212/wnl.43.6.1131. Neurology. 1993. PMID: 8170557

9

Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval.

Rodius F, Duclos F, Wrogemann K, Le Paslier D, Ougen P, Billault A, Belal S, Musenger C, Brice A, Dürr A, et al. Rodius F, et al. Among authors: durr a. Am J Hum Genet. 1994 Jun;54(6):1050-9. Am J Hum Genet. 1994. PMID: 8198128 Free PMC article.

10

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. Neurology. 1993 Nov;43(11):2212-4. doi: 10.1212/wnl.43.11.2212. Neurology. 1993. PMID: 8232931

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