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9. [A girl with hereditary myotonia due to an exceptional sodium channel mutation]. van den Bergen JC; Verbruggen KT; Ginjaar HB; Kerstjens-Frederikse WS Ned Tijdschr Geneeskd; 2006 Nov; 150(45):2501-6. PubMed ID: 17137100 [TBL] [Abstract][Full Text] [Related]
10. A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperature. Bissay V; Keymolen K; Lissens W; Schmedding E; De Keyser J J Neurol Sci; 2011 Sep; 308(1-2):162-4. PubMed ID: 21752396 [TBL] [Abstract][Full Text] [Related]
11. A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene. Schoser BG; Schröder JM; Grimm T; Sternberg D; Kress W Muscle Nerve; 2007 May; 35(5):599-606. PubMed ID: 17212350 [TBL] [Abstract][Full Text] [Related]
12. Isolated eyelid closure myotonia in two families with sodium channel myotonia. Stunnenberg BC; Ginjaar HB; Trip J; Faber CG; van Engelen BG; Drost G Neurogenetics; 2010 May; 11(2):257-60. PubMed ID: 19876661 [TBL] [Abstract][Full Text] [Related]
13. A quantitative measure of handgrip myotonia in non-dystrophic myotonia. Statland JM; Bundy BN; Wang Y; Trivedi JR; Raja Rayan D; Herbelin L; Donlan M; McLin R; Eichinger KJ; Findlater K; Dewar L; Pandya S; Martens WB; Venance SL; Matthews E; Amato AA; Hanna MG; Griggs RC; Barohn RJ; Muscle Nerve; 2012 Oct; 46(4):482-9. PubMed ID: 22987687 [TBL] [Abstract][Full Text] [Related]
14. [Hyperkalemic periodic paralysis: pathophysiology, molecular genetics, and differential diagnosis]. Kurihara T No To Shinkei; 1997 Dec; 49(12):1059-66. PubMed ID: 9453036 [No Abstract] [Full Text] [Related]
15. Genotype-phenotype correlations in human skeletal muscle sodium channel diseases. Van den Bergh P; Thonnard JL Arch Neurol; 1995 Nov; 52(11):1045-6. PubMed ID: 7487554 [No Abstract] [Full Text] [Related]