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Abbreviation : SPP
Long Form : sporadic periodic paralysis
No. Year Title Co-occurring Abbreviation
2016 Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis. CI, hypoKPP, OR, TPP
2012 Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis. hypoKPP, TPP
2012 Genotype and phenotype analysis of patients with sporadic periodic paralysis. FPP, HPP
2011 Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis. hypoKPP, TPP
2009 Recurring paralysis. HPP
2006 Mutation screening in Chinese hypokalemic periodic paralysis patients. FPP, hypoKPP, TPP
2005 Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis. FPP, TPP
2003 Diagnosing thyrotoxic periodic paralysis in the ED. HPP, TPP
2001 Hypokalaemia and paralysis. FPP, HPP, TPP, TTKG