Brice A - Search Results

1

Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.

Al-Chalabi A, Dürr A, Wood NW, Parkinson MH, Camuzat A, Hulot JS, Morrison KE, Renton A, Sussmuth SD, Landwehrmeyer BG, Ludolph A, Agid Y, Brice A, Leigh PN, Bensimon G; NNIPPS Genetic Study Group. Al-Chalabi A, et al. Among authors: brice a. PLoS One. 2009 Sep 22;4(9):e7114. doi: 10.1371/journal.pone.0007114. PLoS One. 2009. PMID: 19771175 Free PMC article. Clinical Trial.

2

Association study between iron-related genes polymorphisms and Parkinson's disease.

Borie C, Gasparini F, Verpillat P, Bonnet AM, Agid Y, Hetet G, Brice A, Dürr A, Grandchamp B; French Parkinson's disease genetic study group. Borie C, et al. Among authors: brice a. J Neurol. 2002 Jul;249(7):801-4. doi: 10.1007/s00415-002-0704-6. J Neurol. 2002. PMID: 12140659

3

Spinocerebellar ataxias caused by polyglutamine expansions.

Stevanin G, Dürr A, Brice A. Stevanin G, et al. Among authors: brice a. Adv Exp Med Biol. 2002;516:47-77. doi: 10.1007/978-1-4615-0117-6_3. Adv Exp Med Biol. 2002. PMID: 12611435 Review. No abstract available.

4

Prevalence of dentatorubral-pallidoluysian atrophy in a large series of white patients with cerebellar ataxia.

Le Ber I, Camuzat A, Castelnovo G, Azulay JP, Genton P, Gastaut JL, Broglin D, Labauge P, Brice A, Durr A. Le Ber I, et al. Among authors: brice a. Arch Neurol. 2003 Aug;60(8):1097-9. doi: 10.1001/archneur.60.8.1097. Arch Neurol. 2003. PMID: 12925365

5

Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.

Lücking CB, Chesneau V, Lohmann E, Verpillat P, Dulac C, Bonnet AM, Gasparini F, Agid Y, Dürr A, Brice A. Lücking CB, et al. Among authors: brice a. Arch Neurol. 2003 Sep;60(9):1253-6. doi: 10.1001/archneur.60.9.1253. Arch Neurol. 2003. PMID: 12975291

6

PARK11 is not linked with Parkinson's disease in European families.

Prestel J, Sharma M, Leitner P, Zimprich A, Vaughan JR, Dürr A, Bonifati V, De Michele G, Hanagasi HA, Farrer M, Hofer A, Asmus F, Volpe G, Meco G, Brice A, Wood NW, Müller-Myhsok B, Gasser T; European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD). Prestel J, et al. Among authors: brice a. Eur J Hum Genet. 2005 Feb;13(2):193-7. doi: 10.1038/sj.ejhg.5201317. Eur J Hum Genet. 2005. PMID: 15523496

7

Spinocerebellar ataxia with mental retardation (SCA13).

Stevanin G, Durr A, Benammar N, Brice A. Stevanin G, et al. Among authors: brice a. Cerebellum. 2005;4(1):43-6. doi: 10.1080/14734220510007923. Cerebellum. 2005. PMID: 15895558 Review.

8

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: brice a. Arch Neurol. 2005 Jun;62(6):962-6. doi: 10.1001/archneur.62.6.962. Arch Neurol. 2005. PMID: 15956167

9

New autosomal recessive cerebellar ataxias with oculomotor apraxia.

Le Ber I, Brice A, Dürr A. Le Ber I, et al. Among authors: brice a. Curr Neurol Neurosci Rep. 2005 Sep;5(5):411-7. doi: 10.1007/s11910-005-0066-4. Curr Neurol Neurosci Rep. 2005. PMID: 16131425 Review.

10

[LRRK2 is a major gene in North African parkinsonism].

Lesage S, Dürr A, Brice A. Lesage S, et al. Among authors: brice a. Med Sci (Paris). 2006 May;22(5):470-1. doi: 10.1051/medsci/2006225470. Med Sci (Paris). 2006. PMID: 16687108 Free article. French. No abstract available.

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