Sternberg D - Search Results

1

Diagnostic yield of a practical electrodiagnostic protocol discriminating between different congenital myasthenic syndromes.

Stojkovic T, Masingue M, Turmel H, Hezode-Arzel M, Béhin A, Leonard-Louis S, Bassez G, Bauché S, Blondy P, Richard P, Sternberg D, Eymard B, Fournier E, Villar-Quiles RN. Stojkovic T, et al. Among authors: sternberg d. Neuromuscul Disord. 2022 Dec;32(11-12):870-878. doi: 10.1016/j.nmd.2022.10.001. Epub 2022 Oct 9. Neuromuscul Disord. 2022. PMID: 36522822

2

Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.

Sternberg D, Chatzoglou E, Laforêt P, Fayet G, Jardel C, Blondy P, Fardeau M, Amselem S, Eymard B, Lombès A. Sternberg D, et al. Brain. 2001 May;124(Pt 5):984-94. doi: 10.1093/brain/124.5.984. Brain. 2001. PMID: 11335700

3

Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function.

Fayet G, Jansson M, Sternberg D, Moslemi AR, Blondy P, Lombès A, Fardeau M, Oldfors A. Fayet G, et al. Among authors: sternberg d. Neuromuscul Disord. 2002 Jun;12(5):484-93. doi: 10.1016/s0960-8966(01)00332-7. Neuromuscul Disord. 2002. PMID: 12031622

4

[Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation].

Auré K, Sternberg D, Maisonobe T, Herson S, Jardel C, Blondy P, Lombès A, Eymard B, Laforêt P. Auré K, et al. Among authors: sternberg d. Rev Neurol (Paris). 2003 Dec;159(12):1163-8. Rev Neurol (Paris). 2003. PMID: 14978417 French.

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

A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification.

Ferriby D, Stojkovic T, Sternberg D, Hurtevent JF, Hurtevent JP, Vermersch P. Ferriby D, et al. Among authors: sternberg d. Neuromuscul Disord. 2006 May;16(5):321-4. doi: 10.1016/j.nmd.2006.01.015. Epub 2006 Apr 19. Neuromuscul Disord. 2006. PMID: 16624558

8

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

9

Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder.

Fontaine B, Fournier E, Sternberg D, Vicart S, Tabti N. Fontaine B, et al. Among authors: sternberg d. Neurotherapeutics. 2007 Apr;4(2):225-32. doi: 10.1016/j.nurt.2007.01.002. Neurotherapeutics. 2007. PMID: 17395132 Free article. Review.

10

Glucocorticoids may trigger attacks in several types of periodic paralysis.

Arzel-Hézode M, McGoey S, Sternberg D, Vicart S, Eymard B, Fontaine B. Arzel-Hézode M, et al. Among authors: sternberg d. Neuromuscul Disord. 2009 Mar;19(3):217-9. doi: 10.1016/j.nmd.2008.12.008. Epub 2009 Feb 7. Neuromuscul Disord. 2009. PMID: 19201608

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