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11. Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families. Sillén A; Sørensen T; Kantola I; Friis ML; Gustavson KH; Wadelius C Am J Med Genet; 1997 Mar; 69(1):102-6. PubMed ID: 9066893 [TBL] [Abstract][Full Text] [Related]
12. Muscle fiber conduction velocity in the diagnosis of sporadic hypokalemic periodic paralysis. Brouwer OF; Zwarts MJ; Links TP; Wintzen AR Clin Neurol Neurosurg; 1992; 94(2):149-51. PubMed ID: 1324813 [TBL] [Abstract][Full Text] [Related]
13. Myopathy of hypokalemic periodic paralysis. An electron microscopic study. Macdonald RD; Rewcastle NB; Humphrey JG Arch Neurol; 1969 Jun; 20(6):565-85. PubMed ID: 5769838 [No Abstract] [Full Text] [Related]
14. Familial hypokalemic paralysis: a case study. Campanile S; Montagna P; Agati R; Campanile A; Lorusso S Riv Patol Nerv Ment; 1984; 105(3):113-8. PubMed ID: 6571450 [TBL] [Abstract][Full Text] [Related]
16. Long-standing bidirectional tachycardia in a patient with hypokalemic periodic paralysis. Fukuda K; Ogawa S; Yokozuka H; Handa S; Nakamura Y J Electrocardiol; 1988 Jan; 21(1):71-5. PubMed ID: 3351412 [TBL] [Abstract][Full Text] [Related]
17. Dominant-inherited hypokalemic periodic paralysis in a large Chinese family. Yeh JH; Sun MH; Chiu HC J Formos Med Assoc; 1999 Apr; 98(4):277-82. PubMed ID: 10389373 [TBL] [Abstract][Full Text] [Related]
18. [Clinical and molecular genetic analysis of a family with normokalemic periodic paralysis]. Wei CJ; Wang D; Wang S; Jiao H; Hong DJ; Pu LH; Xiong H Zhonghua Er Ke Za Zhi; 2013 Jan; 51(1):47-51. PubMed ID: 23527931 [TBL] [Abstract][Full Text] [Related]