RiggsJE. The periodic paralysesNeurol Clin1988;6:485–98
3.
JohnsenT. Familial periodic paralysis with hypokalemicDan Med Bull1981;28:1–27
4.
BrouwerOFZwartsMJLinksTP. Muscle fiber conduction velocity in the diagnosis of sporadic hypokalemic periodic paralysisClin Neurol Neurosurg1992;94:149–51
5.
KantolaIMTarssanenLT. Diagnosis of familial hypokalemic periodic paralysis: Role of the potassium exercise testNeurology1992;42:2158–61
6.
KantolaIMTarssanenLT. Familial hypokalemic periodic paralysis in FinlandJ Neurol Neurosurg Psychiatry1992;55:322–4
7.
KramerLDColeJPMessengerJC. Cardiac dysfunction in a patient with familial hypokalemic periodic paralysisChest1979;75:189–92
LinksTPSmitAJOosterhuisHJ. Potassium channels in hypokalemic periodic paralysis: A key to the pathogenesis?Clin Sci (Colch)1993;85:319–25
10.
FontaineBVale-SantosJEJurkatt-RottK. Mapping of the hypokalemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European familiesNat Genet1994;6:267–72
11.
ElbazAVale-SantosJJurkat-RottK. Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): Genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 Caucasian familiesAm J Hum Genet1995;56:374–80
12.
LapiePGoudetCNargeotJ. Electrophysiological properties of the hypokalemic periodic paralysis mutation (R528H) of the skeletal muscle alpha 1s subunit as expressed in mouse L cellsFEBS Lett1996;382:244–8