Fontaine B - Search Results

1

The primary periodic paralyses: diagnosis, pathogenesis and treatment.

Venance SL, Cannon SC, Fialho D, Fontaine B, Hanna MG, Ptacek LJ, Tristani-Firouzi M, Tawil R, Griggs RC; CINCH investigators. Venance SL, et al. Among authors: fontaine b. Brain. 2006 Jan;129(Pt 1):8-17. doi: 10.1093/brain/awh639. Epub 2005 Sep 29. Brain. 2006. PMID: 16195244 Review.

2

The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.

Matthews E, Fialho D, Tan SV, Venance SL, Cannon SC, Sternberg D, Fontaine B, Amato AA, Barohn RJ, Griggs RC, Hanna MG; CINCH Investigators. Matthews E, et al. Among authors: fontaine b. Brain. 2010 Jan;133(Pt 1):9-22. doi: 10.1093/brain/awp294. Epub 2009 Nov 16. Brain. 2010. PMID: 19917643 Free PMC article. Review.

3

Diagnosis and new treatment in muscle channelopathies.

Meola G, Hanna MG, Fontaine B. Meola G, et al. Among authors: fontaine b. J Neurol Neurosurg Psychiatry. 2009 Apr;80(4):360-5. doi: 10.1136/jnnp.2008.164046. J Neurol Neurosurg Psychiatry. 2009. PMID: 19289476 Review.

4

Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotype.

Matthews E, Guet A, Mayer M, Vicart S, Pemble S, Sternberg D, Fontaine B, Hanna MG. Matthews E, et al. Among authors: fontaine b. Neurology. 2008 Nov 18;71(21):1740-2. doi: 10.1212/01.wnl.0000335269.21550.0e. Neurology. 2008. PMID: 19015492 Free PMC article. No abstract available.

5

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

6

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

7

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: fontaine b. Neurology. 2004 Dec 14;63(11):2120-7. doi: 10.1212/01.wnl.0000145768.09934.ec. Neurology. 2004. PMID: 15596759

8

Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder.

Lion-Francois L, Mignot C, Vicart S, Manel V, Sternberg D, Landrieu P, Lesca G, Broussolle E, Billette de Villemeur T, Napuri S, des Portes V, Fontaine B. Lion-Francois L, et al. Among authors: fontaine b. Neurology. 2010 Aug 17;75(7):641-5. doi: 10.1212/WNL.0b013e3181ed9e96. Neurology. 2010. PMID: 20713951

9

Unravelling the pathophysiology of calcium channel mutations causing neurological disorders.

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

10

EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders.

Burgunder JM, Schöls L, Baets J, Andersen P, Gasser T, Szolnoki Z, Fontaine B, Van Broeckhoven C, Di Donato S, De Jonghe P, Lynch T, Mariotti C, Spinazzola A, Tabrizi SJ, Tallaksen C, Zeviani M, Harbo HF, Finsterer J. Burgunder JM, et al. Among authors: fontaine b. Eur J Neurol. 2011 Feb;18(2):207-217. doi: 10.1111/j.1468-1331.2010.03069.x. Eur J Neurol. 2011. PMID: 20500522

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