Lebre AS - Search Results

1

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Stevanin G, Fujigasaki H, Lebre AS, Camuzat A, Jeannequin C, Dode C, Takahashi J, San C, Bellance R, Brice A, Durr A. Stevanin G, et al. Among authors: lebre as. Brain. 2003 Jul;126(Pt 7):1599-603. doi: 10.1093/brain/awg155. Epub 2003 May 6. Brain. 2003. PMID: 12805114

2

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.

Cancel G, Dürr A, Didierjean O, Imbert G, Bürk K, Lezin A, Belal S, Benomar A, Abada-Bendib M, Vial C, Guimarães J, Chneiweiss H, Stevanin G, Yvert G, Abbas N, Saudou F, Lebre AS, Yahyaoui M, Hentati F, Vernant JC, Klockgether T, Mandel JL, Agid Y, Brice A. Cancel G, et al. Among authors: lebre as. Hum Mol Genet. 1997 May;6(5):709-15. doi: 10.1093/hmg/6.5.709. Hum Mol Genet. 1997. PMID: 9158145

3

Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codon.

Stevanin G, Lebre AS, Mathieux C, Cancel G, Abbas N, Didierjean O, Dürr A, Trottier Y, Agid Y, Brice A. Stevanin G, et al. Among authors: lebre as. Am J Hum Genet. 1997 Jun;60(6):1548-52. doi: 10.1016/S0002-9297(07)64251-7. Am J Hum Genet. 1997. PMID: 9199580 Free PMC article. No abstract available.

4

Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).

David G, Dürr A, Stevanin G, Cancel G, Abbas N, Benomar A, Belal S, Lebre AS, Abada-Bendib M, Grid D, Holmberg M, Yahyaoui M, Hentati F, Chkili T, Agid Y, Brice A. David G, et al. Among authors: lebre as. Hum Mol Genet. 1998 Feb;7(2):165-70. doi: 10.1093/hmg/7.2.165. Hum Mol Genet. 1998. PMID: 9425222

5

DYT1 mutation in French families with idiopathic torsion dystonia.

Lebre AS, Durr A, Jedynak P, Ponsot G, Vidailhet M, Agid Y, Brice A. Lebre AS, et al. Brain. 1999 Jan;122 ( Pt 1):41-5. doi: 10.1093/brain/122.1.41. Brain. 1999. PMID: 10050893

6

Distribution of ataxin-7 in normal human brain and retina.

Cancel G, Duyckaerts C, Holmberg M, Zander C, Yvert G, Lebre AS, Ruberg M, Faucheux B, Agid Y, Hirsch E, Brice A. Cancel G, et al. Among authors: lebre as. Brain. 2000 Dec;123 Pt 12:2519-30. doi: 10.1093/brain/123.12.2519. Brain. 2000. PMID: 11099453

7

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family.

Fujigasaki H, Verma IC, Camuzat A, Margolis RL, Zander C, Lebre AS, Jamot L, Saxena R, Anand I, Holmes SE, Ross CA, Dürr A, Brice A. Fujigasaki H, et al. Among authors: lebre as. Ann Neurol. 2001 Jan;49(1):117-21. Ann Neurol. 2001. PMID: 11198281

8

Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions.

Lebre AS, Jamot L, Takahashi J, Spassky N, Leprince C, Ravisé N, Zander C, Fujigasaki H, Kussel-Andermann P, Duyckaerts C, Camonis JH, Brice A. Lebre AS, et al. Hum Mol Genet. 2001 May 15;10(11):1201-13. doi: 10.1093/hmg/10.11.1201. Hum Mol Genet. 2001. PMID: 11371513

9

Zander C, Takahashi J, El Hachimi KH, Fujigasaki H, Albanese V, Lebre AS, Stevanin G, Duyckaerts C, Brice A. Zander C, et al. Among authors: lebre as. Hum Mol Genet. 2001 Oct 15;10(22):2569-79. doi: 10.1093/hmg/10.22.2569. Hum Mol Genet. 2001. PMID: 11709544

10

Two populations of neuronal intranuclear inclusions in SCA7 differ in size and promyelocytic leukaemia protein content.

Takahashi J, Fujigasaki H, Zander C, El Hachimi KH, Stevanin G, Dürr A, Lebre AS, Yvert G, Trottier Y, de Thé H, Hauw JJ, Duyckaerts C, Brice A. Takahashi J, et al. Among authors: lebre as. Brain. 2002 Jul;125(Pt 7):1534-43. doi: 10.1093/brain/awf154. Brain. 2002. PMID: 12077003

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