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Page 1
Human skeletal muscle sodium channelopathies.
Vicart S, Sternberg D, Fontaine B, Meola G. Vicart S, et al. Among authors: fontaine b. Neurol Sci. 2005 Oct;26(4):194-202. doi: 10.1007/s10072-005-0461-x. Neurol Sci. 2005. PMID: 16193245 Review.
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia.
Furby A, Vicart S, Camdessanché JP, Fournier E, Chabrier S, Lagrue E, Paricio C, Blondy P, Touraine R, Sternberg D, Fontaine B. Furby A, et al. Among authors: fontaine b. Neuromuscul Disord. 2014 Nov;24(11):953-9. doi: 10.1016/j.nmd.2014.06.439. Epub 2014 Jul 2. Neuromuscul Disord. 2014. PMID: 25088311
Periodic paralysis and voltage-gated ion channels.
Fontaine B, Lapie P, Plassart E, Tabti N, Nicole S, Reboul J, Rime-Davoine CS. Fontaine B, et al. Kidney Int. 1996 Jan;49(1):9-18. doi: 10.1038/ki.1996.2. Kidney Int. 1996. PMID: 8770943 Free article. Review. No abstract available.
479 results