Sternberg D - Search Results

1

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

2

["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].

Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A. Laforêt P, et al. Among authors: sternberg d. Rev Neurol (Paris). 2000 Dec;156(12):1136-47. Rev Neurol (Paris). 2000. PMID: 11139730 French.

3

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

4

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

5

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

6

[Periodic paralysis discovered in a 65-year-old woman: one case report].

Decaux O, Poinsignon Y, Rosenbaum D, Sternberg D, Bouissiere-Jardel J, Jardel H. Decaux O, et al. Among authors: sternberg d. Rev Med Interne. 2003 Jan;24(1):55-8. doi: 10.1016/s0248-8663(02)00006-1. Rev Med Interne. 2003. PMID: 12614859 French.

7

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

8

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.

9

[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.

10

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.

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