Tabti N - Search Results

1

Cold extends electromyography distinction between ion channel mutations causing myotonia.

Fournier E, Viala K, Gervais H, Sternberg D, Arzel-Hézode M, Laforêt P, Eymard B, Tabti N, Willer JC, Vial C, Fontaine B. Fournier E, et al. Among authors: tabti n. Ann Neurol. 2006 Sep;60(3):356-65. doi: 10.1002/ana.20905. Ann Neurol. 2006. PMID: 16786525

2

Electromyography guides toward subgroups of mutations in muscle channelopathies.

Fournier E, Arzel M, Sternberg D, Vicart S, Laforet P, Eymard B, Willer JC, Tabti N, Fontaine B. Fournier E, et al. Among authors: tabti n. Ann Neurol. 2004 Nov;56(5):650-61. doi: 10.1002/ana.20241. Ann Neurol. 2004. PMID: 15389891 Clinical Trial.

3

Clinical electrophysiology of muscle diseases and episodic muscle disorders.

Fournier E, Tabti N. Fournier E, et al. Among authors: tabti n. Handb Clin Neurol. 2019;161:269-280. doi: 10.1016/B978-0-444-64142-7.00053-9. Handb Clin Neurol. 2019. PMID: 31307605 Review.

4

Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis.

Sternberg D, Tabti N, Fournier E, Hainque B, Fontaine B. Sternberg D, et al. Among authors: tabti n. Neurology. 2003 Sep 23;61(6):857-9. doi: 10.1212/01.wnl.0000082392.66713.e3. Neurology. 2003. PMID: 14504341

5

Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans.

Bouhours M, Sternberg D, Davoine CS, Ferrer X, Willer JC, Fontaine B, Tabti N. Bouhours M, et al. Among authors: tabti n. J Physiol. 2004 Feb 1;554(Pt 3):635-47. doi: 10.1113/jphysiol.2003.053082. Epub 2003 Nov 14. J Physiol. 2004. PMID: 14617673 Free PMC article.

6

A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivation.

Bouhours M, Luce S, Sternberg D, Willer JC, Fontaine B, Tabti N. Bouhours M, et al. Among authors: tabti n. J Physiol. 2005 Jun 1;565(Pt 2):415-27. doi: 10.1113/jphysiol.2004.081018. Epub 2005 Mar 24. J Physiol. 2005. PMID: 15790667 Free PMC article.

7

Cold-induced disruption of Na+ channel slow inactivation underlies paralysis in highly thermosensitive paramyotonia.

Carle T, Fournier E, Sternberg D, Fontaine B, Tabti N. Carle T, et al. Among authors: tabti n. J Physiol. 2009 Apr 15;587(Pt 8):1705-14. doi: 10.1113/jphysiol.2008.165787. Epub 2009 Feb 16. J Physiol. 2009. PMID: 19221125 Free PMC article.

8

Homozygosity for dominant mutations increases severity of muscle channelopathies.

Arzel-Hézode M, Sternberg D, Tabti N, Vicart S, Goizet C, Eymard B, Fontaine B, Fournier E. Arzel-Hézode M, et al. Among authors: tabti n. Muscle Nerve. 2010 Apr;41(4):470-7. doi: 10.1002/mus.21520. Muscle Nerve. 2010. PMID: 19882638

9

Unravelling the pathophysiology of calcium channel mutations causing neurological disorders.

Fontaine B, Tabti N. Fontaine B, et al. Among authors: tabti n. Brain. 2000 Mar;123 Pt 3:423-4. doi: 10.1093/brain/123.3.423. Brain. 2000. PMID: 10686168 No abstract available.

10

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.

Sternberg D, Maisonobe T, Jurkat-Rott K, Nicole S, Launay E, Chauveau D, Tabti N, Lehmann-Horn F, Hainque B, Fontaine B. Sternberg D, et al. Among authors: tabti n. Brain. 2001 Jun;124(Pt 6):1091-9. doi: 10.1093/brain/124.6.1091. Brain. 2001. PMID: 11353725

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