Grid D - Search Results

1

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. Among authors: grid d. Neuromuscul Disord. 2002 Nov;12(9):849-52. doi: 10.1016/s0960-8966(02)00029-9. Neuromuscul Disord. 2002. PMID: 12398836 Clinical Trial.

2

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. Among authors: grid d. 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

3

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: grid d. 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

4

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: grid d. Neuromuscul Disord. 2000 Dec;10(8):592-8. doi: 10.1016/s0960-8966(00)00141-3. Neuromuscul Disord. 2000. PMID: 11053687

5

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: grid d. Neuromuscul Disord. 2003 Jan;13(1):60-7. doi: 10.1016/s0960-8966(02)00196-7. Neuromuscul Disord. 2003. PMID: 12467734

6

A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease.

Kessali M, Zemmouri R, Guilbot A, Maisonobe T, Brice A, LeGuern E, Grid D. Kessali M, et al. Among authors: grid d. Neurology. 1997 Apr;48(4):867-73. doi: 10.1212/wnl.48.4.867. Neurology. 1997. PMID: 9109869

7

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. Among authors: grid d. Brain. 2004 Jan;127(Pt 1):154-63. doi: 10.1093/brain/awh021. Epub 2003 Nov 7. Brain. 2004. PMID: 14607793

8

Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients.

Tazir M, Ali-Pacha L, M'Zahem A, Delaunoy JP, Fritsch M, Nouioua S, Benhassine T, Assami S, Grid D, Vallat JM, Hamri A, Koenig M. Tazir M, et al. Among authors: grid d. J Neurol Sci. 2009 Mar 15;278(1-2):77-81. doi: 10.1016/j.jns.2008.12.004. Epub 2009 Jan 11. J Neurol Sci. 2009. PMID: 19141356

9

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.

De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N. De Sandre-Giovannoli A, et al. Among authors: grid d. Am J Hum Genet. 2002 Mar;70(3):726-36. doi: 10.1086/339274. Epub 2002 Jan 17. Am J Hum Genet. 2002. PMID: 11799477 Free PMC article.

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: grid d. Curr Neurol Neurosci Rep. 2004 Sep;4(5):413-9. Curr Neurol Neurosci Rep. 2004. PMID: 15324608

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