Brice A - Search Results

1

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.

Klebe S, Lacour A, Durr A, Stojkovic T, Depienne C, Forlani S, Poea-Guyon S, Vuillaume I, Sablonniere B, Vermersch P, Brice A, Stevanin G. Klebe S, et al. Among authors: brice a. Neurogenetics. 2007 Apr;8(2):155-7. doi: 10.1007/s10048-006-0074-9. Epub 2007 Jan 5. Neurogenetics. 2007. PMID: 17205300 No abstract available.

2

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.

3

PML nuclear bodies and neuronal intranuclear inclusion in polyglutamine diseases.

Takahashi J, Fujigasaki H, Iwabuchi K, Bruni AC, Uchihara T, El Hachimi KH, Stevanin G, Dürr A, Lebre AS, Trottier Y, de Thé H, Tanaka J, Hauw JJ, Duyckaerts C, Brice A. Takahashi J, et al. Among authors: brice a. Neurobiol Dis. 2003 Aug;13(3):230-7. doi: 10.1016/s0969-9961(03)00080-9. Neurobiol Dis. 2003. PMID: 12901837

4

Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.

Stevanin G, Bouslam N, Thobois S, Azzedine H, Ravaux L, Boland A, Schalling M, Broussolle E, Dürr A, Brice A. Stevanin G, et al. Among authors: brice a. Ann Neurol. 2004 Jan;55(1):97-104. doi: 10.1002/ana.10798. Ann Neurol. 2004. PMID: 14705117

5

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A.

Abel A, Fonknechten N, Hofer A, Dürr A, Cruaud C, Voit T, Weissenbach J, Brice A, Klimpe S, Auburger G, Hazan J. Abel A, et al. Among authors: brice a. Neurogenetics. 2004 Dec;5(4):239-43. doi: 10.1007/s10048-004-0191-2. Epub 2004 Oct 28. Neurogenetics. 2004. PMID: 15517445

6

Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia.

Dürr A, Camuzat A, Colin E, Tallaksen C, Hannequin D, Coutinho P, Fontaine B, Rossi A, Gil R, Rousselle C, Ruberg M, Stevanin G, Brice A. Dürr A, et al. Among authors: brice a. Arch Neurol. 2004 Dec;61(12):1867-72. doi: 10.1001/archneur.61.12.1867. Arch Neurol. 2004. PMID: 15596607

7

Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort.

van de Warrenburg BP, Hendriks H, Dürr A, van Zuijlen MC, Stevanin G, Camuzat A, Sinke RJ, Brice A, Kremer BP. van de Warrenburg BP, et al. Among authors: brice a. Ann Neurol. 2005 Apr;57(4):505-12. doi: 10.1002/ana.20424. Ann Neurol. 2005. PMID: 15747371

8

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).

Bouslam N, Benomar A, Azzedine H, Bouhouche A, Namekawa M, Klebe S, Charon C, Durr A, Ruberg M, Brice A, Yahyaoui M, Stevanin G. Bouslam N, et al. Among authors: brice a. Ann Neurol. 2005 Apr;57(4):567-71. doi: 10.1002/ana.20416. Ann Neurol. 2005. PMID: 15786464

9

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.

10

Spinocerebellar ataxia with sensory neuropathy (SCA25).

Stevanin G, Broussolle E, Streichenberger N, Kopp N, Brice A, Durr A. Stevanin G, et al. Among authors: brice a. Cerebellum. 2005;4(1):58-61. doi: 10.1080/14734220510007932. Cerebellum. 2005. PMID: 15895562

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