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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
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
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
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
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.