Vallat JM - Search Results

1

The various Charcot-Marie-Tooth diseases.

Vallat JM, Mathis S, Funalot B. Vallat JM, et al. Curr Opin Neurol. 2013 Oct;26(5):473-80. doi: 10.1097/WCO.0b013e328364c04b. Curr Opin Neurol. 2013. PMID: 23945280 Review.

2

Nerve biopsy.

Vallat JM, Sindou P, White A. Vallat JM, et al. Curr Opin Neurol. 1995 Oct;8(5):345-8. doi: 10.1097/00019052-199510000-00003. Curr Opin Neurol. 1995. PMID: 8542037 Review.

3

Charcot-Marie-Tooth disease with intermediate motor nerve conduction velocities: characterization of 14 Cx32 mutations in 35 families.

Rouger H, LeGuern E, Birouk N, Gouider R, Tardieu S, Plassart E, Gugenheim M, Vallat JM, Louboutin JP, Bouche P, Agid Y, Brice A. Rouger H, et al. Among authors: vallat jm. Hum Mutat. 1997;10(6):443-52. doi: 10.1002/(SICI)1098-1004(1997)10:6<443::AID-HUMU5>3.0.CO;2-E. Hum Mutat. 1997. PMID: 9401007

4

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

5

[The involvement of myelin proteins in hereditary neuropathies].

Sindou P, Anani T, Garbay B, Couratier P, Lagrange E, Vallat JM. Sindou P, et al. Among authors: vallat jm. Rev Neurol (Paris). 1999 Feb;155(2):97-110. Rev Neurol (Paris). 1999. PMID: 10226313 Review. French.

6

Expression of myelin proteins in the adult heterozygous Trembler mouse.

Vallat JM, Sindou P, Garbay B, Preux PM, Anani T, Richard L, Diot M. Vallat JM, et al. Acta Neuropathol. 1999 Sep;98(3):281-7. doi: 10.1007/s004010051081. Acta Neuropathol. 1999. PMID: 10483786

7

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

8

Ultrastructural immunocytochemical abnormalities of peripheral myelin proteins in hereditary sensory-motor neuropathies: 12 cases.

Anani T, Sindou P, Richard L, Diot M, Vallat JM. Anani T, et al. Among authors: vallat jm. Ann N Y Acad Sci. 1999 Sep 14;883:186-95. Ann N Y Acad Sci. 1999. PMID: 10586244

9

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

10

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

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