Sternberg D - Search Results

1

In vivo and in vitro functional characterization of Andersen's syndrome mutations.

Bendahhou S, Fournier E, Sternberg D, Bassez G, Furby A, Sereni C, Donaldson MR, Larroque MM, Fontaine B, Barhanin J. Bendahhou S, et al. Among authors: sternberg d. J Physiol. 2005 Jun 15;565(Pt 3):731-41. doi: 10.1113/jphysiol.2004.081620. Epub 2005 Apr 14. J Physiol. 2005. PMID: 15831539 Free PMC article.

2

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. Brain. 2001 Jun;124(Pt 6):1091-9. doi: 10.1093/brain/124.6.1091. Brain. 2001. PMID: 11353725

3

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. Neurology. 2003 Sep 23;61(6):857-9. doi: 10.1212/01.wnl.0000082392.66713.e3. Neurology. 2003. PMID: 14504341

4

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: sternberg d. 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.

5

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: sternberg d. Ann Neurol. 2004 Nov;56(5):650-61. doi: 10.1002/ana.20241. Ann Neurol. 2004. PMID: 15389891 Clinical Trial.

6

New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.

Vicart S, Sternberg D, Fournier E, Ochsner F, Laforet P, Kuntzer T, Eymard B, Hainque B, Fontaine B. Vicart S, et al. Among authors: sternberg d. Neurology. 2004 Dec 14;63(11):2120-7. doi: 10.1212/01.wnl.0000145768.09934.ec. Neurology. 2004. PMID: 15596759

7

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: sternberg d. 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.

8

Human skeletal muscle sodium channelopathies.

Vicart S, Sternberg D, Fontaine B, Meola G. Vicart S, et al. Among authors: sternberg d. Neurol Sci. 2005 Oct;26(4):194-202. doi: 10.1007/s10072-005-0461-x. Neurol Sci. 2005. PMID: 16193245 Review.

9

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: sternberg d. Ann Neurol. 2006 Sep;60(3):356-65. doi: 10.1002/ana.20905. Ann Neurol. 2006. PMID: 16786525

10

Gating defects of a novel Na+ channel mutant causing hypokalemic periodic paralysis.

Carle T, Lhuillier L, Luce S, Sternberg D, Devuyst O, Fontaine B, Tabti N. Carle T, et al. Among authors: sternberg d. Biochem Biophys Res Commun. 2006 Sep 22;348(2):653-61. doi: 10.1016/j.bbrc.2006.07.101. Epub 2006 Jul 28. Biochem Biophys Res Commun. 2006. PMID: 16890191

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