Tazir M - Search Results

1

Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathy.

Zemmouri R, Azzedine H, Assami S, Kitouni N, Vallat JM, Maisonobe T, Hamadouche T, Kessaci M, Mansouri B, Le Guern E, Grid D, Tazir M. Zemmouri R, et al. Among authors: tazir m. Neuromuscul Disord. 2000 Dec;10(8):592-8. doi: 10.1016/s0960-8966(00)00141-3. Neuromuscul Disord. 2000. PMID: 11053687

2

[Autosomal recessive forms of Charcot-Marie-Tooth disease].

Vallat JM, Grid D, Magdelaine C, Sturtz F, Levy N, Tazir M. Vallat JM, et al. Among authors: tazir m. Bull Acad Natl Med. 2005 Jan;189(1):55-68; discussion 68-9. Bull Acad Natl Med. 2005. PMID: 16119880 Review. French.

3

Phenotypic variability in giant axonal neuropathy.

Tazir M, Nouioua S, Magy L, Huehne K, Assami S, Urtizberea A, Grid D, Hamadouche T, Rautenstrauss B, Vallat JM. Tazir M, et al. Neuromuscul Disord. 2009 Apr;19(4):270-4. doi: 10.1016/j.nmd.2009.01.011. Epub 2009 Feb 23. Neuromuscul Disord. 2009. PMID: 19231187

4

Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes.

Nouioua S, Hamadouche T, Funalot B, Bernard R, Bellatache N, Bouderba R, Grid D, Assami S, Benhassine T, Levy N, Vallat JM, Tazir M. Nouioua S, et al. Among authors: tazir m. Neuromuscul Disord. 2011 Aug;21(8):543-50. doi: 10.1016/j.nmd.2011.04.013. Epub 2011 Jul 7. Neuromuscul Disord. 2011. PMID: 21741241

5

Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease.

Mathis S, Corcia P, Tazir M, Camu W, Magdelaine C, Latour P, Biberon J, Guennoc AM, Richard L, Magy L, Funalot B, Vallat JM. Mathis S, et al. Among authors: tazir m. Neuromuscul Disord. 2014 Jun;24(6):524-8. doi: 10.1016/j.nmd.2014.03.014. Epub 2014 Apr 13. Neuromuscul Disord. 2014. PMID: 24792522

6

Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update.

Tazir M, Hamadouche T, Nouioua S, Mathis S, Vallat JM. Tazir M, et al. J Neurol Sci. 2014 Dec 15;347(1-2):14-22. doi: 10.1016/j.jns.2014.10.013. Epub 2014 Oct 16. J Neurol Sci. 2014. PMID: 25454638 Review.

7

Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1.

Tazir M, Vallat JM, Bomont P, Zemmouri R, Sindou P, Assami S, Nouioua S, Hammadouche T, Grid D, Koenig M. Tazir M, et al. Neuromuscul Disord. 2002 Nov;12(9):849-52. doi: 10.1016/s0960-8966(02)00029-9. Neuromuscul Disord. 2002. PMID: 12398836 Clinical Trial.

8

The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene.

Chaouch M, Allal Y, De Sandre-Giovannoli A, Vallat JM, Amer-el-Khedoud A, Kassouri N, Chaouch A, Sindou P, Hammadouche T, Tazir M, Lévy N, Grid D. Chaouch M, et al. Among authors: tazir m. Neuromuscul Disord. 2003 Jan;13(1):60-7. doi: 10.1016/s0960-8966(02)00196-7. Neuromuscul Disord. 2003. PMID: 12467734

9

Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C.

Tazir M, Azzedine H, Assami S, Sindou P, Nouioua S, Zemmouri R, Hamadouche T, Chaouch M, Feingold J, Vallat JM, Leguern E, Grid D. Tazir M, et al. Brain. 2004 Jan;127(Pt 1):154-63. doi: 10.1093/brain/awh021. Epub 2003 Nov 7. Brain. 2004. PMID: 14607793

10

Autosomal recessive forms of Charcot-Marie-Tooth disease.

Vallat JM, Grid D, Magdelaine C, Sturtz F, Tazir M. Vallat JM, et al. Among authors: tazir m. Curr Neurol Neurosci Rep. 2004 Sep;4(5):413-9. Curr Neurol Neurosci Rep. 2004. PMID: 15324608

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