Birouk N - Search Results

1

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: birouk n. 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

2

Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion.

Mouton P, Tardieu S, Gouider R, Birouk N, Maisonobe T, Dubourg O, Brice A, LeGuern E, Bouche P. Mouton P, et al. Among authors: birouk n. Neurology. 1999 Apr 22;52(7):1440-6. doi: 10.1212/wnl.52.7.1440. Neurology. 1999. PMID: 10227632

3

Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness.

Dubourg O, Barhoumi C, Azzedine H, Birouk N, Brice A, Bouche P, Leguern E. Dubourg O, et al. Among authors: birouk n. Muscle Nerve. 2000 Oct;23(10):1508-14. doi: 10.1002/1097-4598(200010)23:10<1508::aid-mus6>3.0.co;2-d. Muscle Nerve. 2000. PMID: 11003785

4

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: birouk n. Neuromuscul Disord. 2001 Jul;11(5):458-63. doi: 10.1016/s0960-8966(00)00222-4. Neuromuscul Disord. 2001. PMID: 11404117

5

Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease.

LeGuern E, Gouider R, Mabin D, Tardieu S, Birouk N, Parent P, Bouche P, Brice A. LeGuern E, et al. Among authors: birouk n. Ann Neurol. 1997 Jan;41(1):104-8. doi: 10.1002/ana.410410117. Ann Neurol. 1997. PMID: 9005872

6

Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases.

Birouk N, Gouider R, Le Guern E, Gugenheim M, Tardieu S, Maisonobe T, Le Forestier N, Agid Y, Brice A, Bouche P. Birouk N, et al. Brain. 1997 May;120 ( Pt 5):813-23. doi: 10.1093/brain/120.5.813. Brain. 1997. PMID: 9183252

7

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. Neurology. 1998 Apr;50(4):1074-82. doi: 10.1212/wnl.50.4.1074. Neurology. 1998. PMID: 9566397

8

[Multifocal motor neuropathies with conduction blocks. 39 cases].

Le Forestier N, Chassande B, Moulonguet A, Maisonobe T, Schaeffer S, Birouk N, Baumann N, Adams D, Léger JM, Meininger V, Said G, Bouche P. Le Forestier N, et al. Among authors: birouk n. Rev Neurol (Paris). 1997 Oct;153(10):579-86. Rev Neurol (Paris). 1997. PMID: 9684022 French.

9

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

10

[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: birouk n. Rev Neurol (Paris). 1998 Jan;154(1):40-4. Rev Neurol (Paris). 1998. PMID: 9773024 French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

53 results

Search Page

Filters