Cancel G - Search Results

1

Neuronal distribution of intranuclear inclusions in Huntington's disease with adult onset.

Gourfinkel-An I, Cancel G, Duyckaerts C, Faucheux B, Hauw JJ, Trottier Y, Brice A, Agid Y, Hirsch EC. Gourfinkel-An I, et al. Among authors: cancel g. Neuroreport. 1998 Jun 1;9(8):1823-6. doi: 10.1097/00001756-199806010-00028. Neuroreport. 1998. PMID: 9665608

2

Differential distribution of the normal and mutated forms of huntingtin in the human brain.

Gourfinkel-An I, Cancel G, Trottier Y, Devys D, Tora L, Lutz Y, Imbert G, Saudou F, Stevanin G, Agid Y, Brice A, Mandel JL, Hirsch EC. Gourfinkel-An I, et al. Among authors: cancel g. Ann Neurol. 1997 Nov;42(5):712-9. doi: 10.1002/ana.410420507. Ann Neurol. 1997. PMID: 9392570

3

Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions.

Holmberg M, Duyckaerts C, Dürr A, Cancel G, Gourfinkel-An I, Damier P, Faucheux B, Trottier Y, Hirsch EC, Agid Y, Brice A. Holmberg M, et al. Among authors: cancel g. Hum Mol Genet. 1998 May;7(5):913-8. doi: 10.1093/hmg/7.5.913. Hum Mol Genet. 1998. PMID: 9536097

4

Nuclear inclusions in spinocerebellar ataxia type 1.

Duyckaerts C, Dürr A, Cancel G, Brice A. Duyckaerts C, et al. Among authors: cancel g. Acta Neuropathol. 1999 Feb;97(2):201-7. doi: 10.1007/s004010050975. Acta Neuropathol. 1999. PMID: 9928833

5

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. Brain. 2000 Dec;123 Pt 12:2519-30. doi: 10.1093/brain/123.12.2519. Brain. 2000. PMID: 11099453

6

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

7

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: cancel g. 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.

8

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

9

Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.

Stevanin G, Trottier Y, Cancel G, Dürr A, David G, Didierjean O, Bürk K, Imbert G, Saudou F, Abada-Bendib M, Gourfinkel-An I, Benomar A, Abbas N, Klockgether T, Grid D, Agid Y, Mandel JL, Brice A. Stevanin G, et al. Among authors: cancel g. Hum Mol Genet. 1996 Dec;5(12):1887-92. doi: 10.1093/hmg/5.12.1887. Hum Mol Genet. 1996. PMID: 8968739

10

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. Hum Mol Genet. 1997 May;6(5):709-15. doi: 10.1093/hmg/6.5.709. Hum Mol Genet. 1997. PMID: 9158145

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