1Lin SH, Hsu YD, Cheng NL, et al. Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis[ J]. Am J Mod Sci, 2005,329(2) :66-70.
2Dias da silva MR, Cerutti JM, Tengan CH, et al. Mutation linked to familial hypokalaemic periodic paralysis in the calcium channel alphal subunit gene (Carl. 1 ) are not associated with thyrotoxic hypokalaemic periodic paralysis[ J ]. Clin Endocrinol(Oxf), 2002,56(3) : 367-375.
3Kung AW, Lau KS, Fong GC, et al. Association of novel single nude-otide polymorphisms in the calcium channel alphal subunit gene( Carl.1 ) and thyrotoxic periodic paralysis [ J]. J Clin Endocrinol Metab,2004,89(3) : 1340-1345.
4Dias da silva MR, Cerutti JM, Amaldi LA, et al. A mutation in the KC-NE3 potassium channel gene is associated with susceptibility to the thyrotoxie hypokalemic periodic paralysis [ J]. J Clin Endocrinol Metab,2002,87 ( 11 ) : 4881-4884.
5Tang NL,Chow CC,Ko GT, et al. No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients[ J]. Clin Endocrinol (Oxf), 2004,61 ( 1 ) : 109-112.
6Sternberg D,Tabti N,Fournier E, et al. Lack of association of the petassium channel-associated peptide MiRP2-R83H variant with periodic paralysis[J]. Neurology,2003,61(6) :857-859.
7Chen L, Lang D, Ran XW, et al. Clinical and molecular analysis of chinese patients with thyrotoxic periodic paralysis[ J]. Eur Neurol, 2003,49(4) : 227-230.
8Ng WY,Lui KF,Thai AC, et al, Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis[J].Thyroid, 2004,14(3) : 187-190.
9Liu YC ,Tsai WS, Chau T, et al. Acute hypercapnic respiratory failure due to thyrotoxic periodic paralysis[ J ]. Am J Med Sci, 2004,327 (5) :264-267.
10Tassone H, Moulin A, Henderson SO. The pitfalls of potassium replacement in thyrotoxic periodic paralysis : a case report and review of the literature[J] .J Emerg Med,2004,26(2) :157-161.