Vallat JM - Search Results

1

[Ultrastructural lesions of axonal mitochondria in patients with childhood-onset Charcot-Marie-Tooth disease due to MFN2 mutations].

Funalot B, Magdelaine C, Sturtz F, Ouvrier R, Vallat JM. Funalot B, et al. Among authors: vallat jm. Bull Acad Natl Med. 2009 Jan;193(1):151-60; discussion 160-1. Bull Acad Natl Med. 2009. PMID: 19718987 French.

2

Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease.

Sindou P, Vallat JM, Chapon F, Archelos JJ, Tabaraud F, Anani T, Braund KG, Maisonobe T, Hauw JJ, Vandenberghe A. Sindou P, et al. Among authors: vallat jm. Muscle Nerve. 1999 Jan;22(1):99-104. doi: 10.1002/(sici)1097-4598(199901)22:1<99::aid-mus14>3.0.co;2-5. Muscle Nerve. 1999. PMID: 9883862

3

Demyelinating X-linked Charcot-Marie-Tooth disease: unusual electrophysiological findings.

Tabaraud F, Lagrange E, Sindou P, Vandenberghe A, Levy N, Vallat JM. Tabaraud F, et al. Among authors: vallat jm. Muscle Nerve. 1999 Oct;22(10):1442-7. doi: 10.1002/(sici)1097-4598(199910)22:10<1442::aid-mus16>3.0.co;2-6. Muscle Nerve. 1999. PMID: 10487913

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

6

[Importance of the nerve biopsy for the diagnosis of atypical forms of chronic inflammatory demyelinating polyradiculoneuritis: 8 cases].

Vallat JM, Tabaraud F, Magy L, Couratier P. Vallat JM, et al. Bull Acad Natl Med. 2003;187(2):387-99; discussion 399-403. Bull Acad Natl Med. 2003. PMID: 14556448 Review. French.

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

8

Autosomal recessive forms of Charcot-Marie-Tooth disease.

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

9

Autosomal-recessive Charcot-Marie-Tooth diseases.

Vallat JM, Tazir M, Magdelaine C, Sturtz F, Grid D. Vallat JM, et al. J Neuropathol Exp Neurol. 2005 May;64(5):363-70. doi: 10.1093/jnen/64.5.363. J Neuropathol Exp Neurol. 2005. PMID: 15892292 Review.

10

IgG neuropathy: an immunoelectron microscopic study.

Vallat JM, Magy L, Sindou P, Magdelaine C, Cros D. Vallat JM, et al. J Neuropathol Exp Neurol. 2005 May;64(5):386-90. doi: 10.1093/jnen/64.5.386. J Neuropathol Exp Neurol. 2005. PMID: 15892295

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