These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
361 related articles for article (PubMed ID: 11137655)
21. Human muscle voltage-gated ion channels and hereditary disease. Jurkat-Rott K; Lehmann-Horn F Curr Opin Pharmacol; 2001 Jun; 1(3):280-7. PubMed ID: 11712752 [TBL] [Abstract][Full Text] [Related]
22. Idiopathic generalized epilepsy and hypokalemic periodic paralysis in a family of South Indian descent. Subramanian M; Senthil N; Sujatha S Case Rep Neurol Med; 2015; 2015():906049. PubMed ID: 25893123 [TBL] [Abstract][Full Text] [Related]
30. Novel insights into the pathomechanisms of skeletal muscle channelopathies. Burge JA; Hanna MG Curr Neurol Neurosci Rep; 2012 Feb; 12(1):62-9. PubMed ID: 22083238 [TBL] [Abstract][Full Text] [Related]
31. [Ion channels and epilepsy]. Armijo JA; de las Cuevas I; Adín J Rev Neurol; 2000 Jun; 30 Suppl 1():S25-41. PubMed ID: 10904966 [TBL] [Abstract][Full Text] [Related]
32. Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels. Striessnig J; Bolz HJ; Koschak A Pflugers Arch; 2010 Jul; 460(2):361-74. PubMed ID: 20213496 [TBL] [Abstract][Full Text] [Related]
33. Calcium channelopathies in inherited neurological disorders: relevance to drug screening for acquired channel disorders. Lory P; Mezghrani A IDrugs; 2010 Jul; 13(7):467-71. PubMed ID: 20582871 [TBL] [Abstract][Full Text] [Related]
34. Channelopathies. Kim JB Korean J Pediatr; 2014 Jan; 57(1):1-18. PubMed ID: 24578711 [TBL] [Abstract][Full Text] [Related]
35. Neurological channelopathies: diagnosis and therapy in the new millennium. Davies NP; Hanna MG Ann Med; 1999 Dec; 31(6):406-20. PubMed ID: 10680855 [TBL] [Abstract][Full Text] [Related]