Léger JM - Search Results

1

The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity.

Dubourg O, Tardieu S, Birouk N, Gouider R, Léger JM, Maisonobe T, Brice A, Bouche P, LeGuern E. Dubourg O, et al. Among authors: leger jm. Neuromuscul Disord. 2001 Jul;11(5):458-63. doi: 10.1016/s0960-8966(00)00222-4. Neuromuscul Disord. 2001. PMID: 11404117

2

Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion.

Gouider R, LeGuern E, Gugenheim M, Tardieu S, Maisonobe T, Léger JM, Vallat JM, Agid Y, Bouche P, Brice A. Gouider R, et al. Among authors: leger jm. Neurology. 1995 Nov;45(11):2018-23. doi: 10.1212/wnl.45.11.2018. Neurology. 1995. PMID: 7501152

3

Recurrent polyradiculoneuropathy with the 17p11.2 deletion.

Le Forestier N, LeGuern E, Coullin P, Birouk N, Maisonobe T, Brice A, Léger JM, Bouche P. Le Forestier N, et al. Among authors: leger jm. Muscle Nerve. 1997 Sep;20(9):1184-6. doi: 10.1002/(sici)1097-4598(199709)20:9<1184::aid-mus16>3.0.co;2-t. Muscle Nerve. 1997. PMID: 9270678

4

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.

Birouk N, LeGuern E, Maisonobe T, Rouger H, Gouider R, Tardieu S, Gugenheim M, Routon MC, Léger JM, Agid Y, Brice A, Bouche P. Birouk N, et al. Among authors: leger jm. Neurology. 1998 Apr;50(4):1074-82. doi: 10.1212/wnl.50.4.1074. Neurology. 1998. PMID: 9566397

5

[Charcot-Marie-Tooth disease: electromyography is still useful in diagnosis and classification].

Birouk N, Maisonobe T, Le Forestier N, Gouider R, Léger JM, Bouche P. Birouk N, et al. Among authors: leger jm. Rev Neurol (Paris). 1997 Dec;153(12):727-36. Rev Neurol (Paris). 1997. PMID: 9686263 Review. French.

6

Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease.

Dubourg O, Tardieu S, Birouk N, Gouider R, Léger JM, Maisonobe T, Brice A, Bouche P, LeGuern E. Dubourg O, et al. Among authors: leger jm. Brain. 2001 Oct;124(Pt 10):1958-67. doi: 10.1093/brain/124.10.1958. Brain. 2001. PMID: 11571214

7

Proposed revised electrophysiological criteria for chronic inflammatory demyelinating polyradiculoneuropathy.

Nicolas G, Maisonobe T, Le Forestier N, Léger JM, Bouche P. Nicolas G, et al. Among authors: leger jm. Muscle Nerve. 2002 Jan;25(1):26-30. doi: 10.1002/mus.1214. Muscle Nerve. 2002. PMID: 11754181

8

[Multifocal motor neuropathy: a retrospective study of the response to high-dose intravenous immunoglobulin (IVIg) and current perspectives for diagnosis and treatment].

Léger JM, Viala K, Maisonobe T, Bouche P. Léger JM, et al. Bull Acad Natl Med. 2007 Oct;191(7):1395-407; discussion 1407-9. Bull Acad Natl Med. 2007. PMID: 18447061 French.

9

Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group.

LeGuern E, Gouider R, Lopes J, Abbas N, Gugenheim M, Tardieu S, Ravisé N, Léger JM, Vallat JM, Bouche P, et al. LeGuern E, et al. Among authors: leger jm. Hum Mol Genet. 1995 Sep;4(9):1673-4. doi: 10.1093/hmg/4.9.1673. Hum Mol Genet. 1995. PMID: 8541860 No abstract available.

10

Chronic dysimmune demyelinating polyneuropathy: a clinical and electrophysiological study of 93 patients.

Maisonobe T, Chassande B, Vérin M, Jouni M, Léger JM, Bouche P. Maisonobe T, et al. Among authors: leger jm. J Neurol Neurosurg Psychiatry. 1996 Jul;61(1):36-42. doi: 10.1136/jnnp.61.1.36. J Neurol Neurosurg Psychiatry. 1996. PMID: 8676156 Free PMC article.

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