Abada-Bendib M - Search Results

1

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: abada bendib m. Hum Mol Genet. 1998 Feb;7(2):165-70. doi: 10.1093/hmg/7.2.165. Hum Mol Genet. 1998. PMID: 9425222

2

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: abada bendib m. Hum Mol Genet. 1996 Dec;5(12):1887-92. doi: 10.1093/hmg/5.12.1887. Hum Mol Genet. 1996. PMID: 8968739

3

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

4

Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG).

Stevanin G, David G, Dürr A, Giunti P, Benomar A, Abada-Bendib M, Lee MS, Agid Y, Brice A. Stevanin G, et al. Among authors: abada bendib m. Eur J Hum Genet. 1999 Dec;7(8):889-96. doi: 10.1038/sj.ejhg.5200392. Eur J Hum Genet. 1999. PMID: 10602364

5

GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia.

Coutelier M, Burglen L, Mundwiller E, Abada-Bendib M, Rodriguez D, Chantot-Bastaraud S, Rougeot C, Cournelle MA, Milh M, Toutain A, Bacq D, Meyer V, Afenjar A, Deleuze JF, Brice A, Héron D, Stevanin G, Durr A. Coutelier M, et al. Among authors: abada bendib m. Neurology. 2015 Apr 28;84(17):1751-9. doi: 10.1212/WNL.0000000000001524. Epub 2015 Apr 3. Neurology. 2015. PMID: 25841024

6

IFN-γ and TNF-α are involved during Alzheimer disease progression and correlate with nitric oxide production: a study in Algerian patients.

Belkhelfa M, Rafa H, Medjeber O, Arroul-Lammali A, Behairi N, Abada-Bendib M, Makrelouf M, Belarbi S, Masmoudi AN, Tazir M, Touil-Boukoffa C. Belkhelfa M, et al. Among authors: abada bendib m. J Interferon Cytokine Res. 2014 Nov;34(11):839-47. doi: 10.1089/jir.2013.0085. Epub 2014 May 15. J Interferon Cytokine Res. 2014. PMID: 24831467

7

Leber optic hereditary neuropathy plus dystonia.

Mahoui S, Belkhamsa O, Ait Kaci I, Abada Bendib M, Castelnovo G. Mahoui S, et al. Among authors: abada bendib m. Rev Neurol (Paris). 2019 Sep-Oct;175(7-8):483-484. doi: 10.1016/j.neurol.2018.12.011. Epub 2019 Jun 17. Rev Neurol (Paris). 2019. PMID: 31221418 No abstract available.

8

Atypical pantothenate kinase-associated neurodegeneration: Clinical description of two brothers and a review of the literature.

Mahoui S, Benhaddadi A, Ameur El Khedoud W, Abada Bendib M, Chaouch M. Mahoui S, et al. Among authors: abada bendib m. Rev Neurol (Paris). 2017 Dec;173(10):658-662. doi: 10.1016/j.neurol.2017.05.013. Epub 2017 Jun 16. Rev Neurol (Paris). 2017. PMID: 28629633 Review.

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