Bouche P - Search Results

1

[Hereditary neuropathy with liability to pressure palsies].

Bouche P, Mouton P, Gouider R, Dubourg O, Le Guern E, Maisonobe T, le Forestier N. Bouche P, et al. Rev Neurol (Paris). 2000 Oct;156(10):915-9. Rev Neurol (Paris). 2000. PMID: 11033525 Review. French. No abstract available.

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: bouche p. Neurology. 1995 Nov;45(11):2018-23. doi: 10.1212/wnl.45.11.2018. Neurology. 1995. PMID: 7501152

3

Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosis.

LeGuern E, Ravise N, Gouider R, Gugenheim M, Lopes J, Bouche P, Agid Y, Brice A. LeGuern E, et al. Among authors: bouche p. Cytogenet Cell Genet. 1996;72(1):20-5. doi: 10.1159/000134153. Cytogenet Cell Genet. 1996. PMID: 8565626

4

Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.

Lopes J, LeGuern E, Gouider R, Tardieu S, Abbas N, Birouk N, Gugenheim M, Bouche P, Agid Y, Brice A. Lopes J, et al. Among authors: bouche p. Am J Hum Genet. 1996 Jun;58(6):1223-30. Am J Hum Genet. 1996. PMID: 8651299 Free PMC article.

5

A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?

LeGuern E, Gouider R, Ravisé N, Lopes J, Tardieu S, Gugenheim M, Abbas N, Bouche P, Agid Y, Brice A. LeGuern E, et al. Among authors: bouche p. Hum Mol Genet. 1996 Jan;5(1):103-6. doi: 10.1093/hmg/5.1.103. Hum Mol Genet. 1996. PMID: 8789446

6

[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: bouche p. Rev Neurol (Paris). 1997 Dec;153(12):727-36. Rev Neurol (Paris). 1997. PMID: 9686263 Review. French.

7

[Pure motor neuropathy after radiation therapy: 6 cases].

Lalu T, Mercier B, Birouk N, Maisonobe T, Catala M, Le Forestier N, Léger JM, Bouche P. Lalu T, et al. Among authors: bouche p. Rev Neurol (Paris). 1998 Jan;154(1):40-4. Rev Neurol (Paris). 1998. PMID: 9773024 French.

8

[Management of polyneuropathy].

Bouche P, Maisonobe T, Le Forestier N. Bouche P, et al. Rev Neurol (Paris). 1998 Jul;154(6-7):552-6. Rev Neurol (Paris). 1998. PMID: 9773093 French. No abstract available.

9

[True neurological thoracic outlet syndrome].

Le Forestier N, Mouton P, Maisonobe T, Fournier E, Moulonguet A, Willer JC, Bouche P. Le Forestier N, et al. Among authors: bouche p. Rev Neurol (Paris). 2000 Jan;156(1):34-40. Rev Neurol (Paris). 2000. PMID: 10693256 French.

10

Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies.

Dubourg O, Mouton P, Brice A, LeGuern E, Bouche P. Dubourg O, et al. Among authors: bouche p. Neuromuscul Disord. 2000 Mar;10(3):206-8. doi: 10.1016/s0960-8966(99)00103-0. Neuromuscul Disord. 2000. PMID: 10734269 No abstract available.

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