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5. State of the art in hereditary muscle channelopathies. Jurkat-Rott K; Lehmann-Horn F Acta Myol; 2010 Oct; 29(2):343-50. PubMed ID: 21314017 [TBL] [Abstract][Full Text] [Related]
6. [Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders]. Terwindt GM; Ophoff RA; Haan J; Frants RR; Ferrari MD Ned Tijdschr Geneeskd; 1998 May; 142(18):1015-9. PubMed ID: 9623202 [TBL] [Abstract][Full Text] [Related]
8. Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system. Ptácek LJ Neuromuscul Disord; 1997 Jun; 7(4):250-5. PubMed ID: 9196907 [TBL] [Abstract][Full Text] [Related]
9. Genetics, an alternative way to discover, characterize and understand ion channels. Schofield PR Clin Exp Pharmacol Physiol; 2001; 28(1-2):84-8. PubMed ID: 11153544 [TBL] [Abstract][Full Text] [Related]
10. Ion channel shake-down. Ptácek L Nat Genet; 1994 Oct; 8(2):111-2. PubMed ID: 7531055 [No Abstract] [Full Text] [Related]
11. Skeletal muscle channelopathies: new insights into the periodic paralyses and nondystrophic myotonias. Platt D; Griggs R Curr Opin Neurol; 2009 Oct; 22(5):524-31. PubMed ID: 19571750 [TBL] [Abstract][Full Text] [Related]
17. Periodic paralysis, myotonia congenita and sarcolemmal ion channels: a success of the candidate gene approach. Fontaine B Neuromuscul Disord; 1993 Mar; 3(2):101-7. PubMed ID: 7689379 [TBL] [Abstract][Full Text] [Related]
19. Is there a role for potassium channel openers in neuronal ion channel disorders? Lawson K Expert Opin Investig Drugs; 2000 Oct; 9(10):2269-80. PubMed ID: 11060806 [TBL] [Abstract][Full Text] [Related]
20. Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group. Terwindt GM; Ophoff RA; Haan J; Sandkuijl LA; Frants RR; Ferrari MD Eur J Hum Genet; 1998; 6(4):297-307. PubMed ID: 9781035 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]