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Journal Abstract Search
347 related items for PubMed ID: 9307251
1. Andersen's syndrome: a distinct periodic paralysis. Sansone V, Griggs RC, Meola G, Ptácek LJ, Barohn R, Iannaccone S, Bryan W, Baker N, Janas SJ, Scott W, Ririe D, Tawil R. Ann Neurol; 1997 Sep; 42(3):305-12. PubMed ID: 9307251 [Abstract] [Full Text] [Related]
3. In vivo and in vitro functional characterization of Andersen's syndrome mutations. Bendahhou S, Fournier E, Sternberg D, Bassez G, Furby A, Sereni C, Donaldson MR, Larroque MM, Fontaine B, Barhanin J. J Physiol; 2005 Jun 15; 565(Pt 3):731-41. PubMed ID: 15831539 [Abstract] [Full Text] [Related]
9. Mutation screening in Chinese hypokalemic periodic paralysis patients. Wang W, Jiang L, Ye L, Zhu N, Su T, Guan L, Li X, Ning G. Mol Genet Metab; 2006 Apr 15; 87(4):359-63. PubMed ID: 16386935 [Abstract] [Full Text] [Related]
10. Different gene loci for hyperkalemic and hypokalemic periodic paralysis. Fontaine B, Trofatter J, Rouleau GA, Khurana TS, Haines J, Brown R, Gusella JF. Neuromuscul Disord; 1991 Apr 15; 1(4):235-8. PubMed ID: 1822800 [Abstract] [Full Text] [Related]
11. A proposed mutation, Val781Ile, associated with hyperkalemic periodic paralysis and cardiac dysrhythmia is a benign polymorphism. Green DS, Hayward LJ, George AL, Cannon SC. Ann Neurol; 1997 Aug 15; 42(2):253-6. PubMed ID: 9266738 [Abstract] [Full Text] [Related]
12. Hyperthyroidism with periodic paralysis. Feldman DL, Goldberg WM. Can Med Assoc J; 1969 Nov 29; 101(11):61-5. PubMed ID: 5353150 [Abstract] [Full Text] [Related]
13. Molecular basis for hyperkalemic periodic paralysis. Brown RH. Int J Neurol; 1969 Nov 29; 25-26():89-96. PubMed ID: 11980067 [Abstract] [Full Text] [Related]
18. Normokalemic periodic paralysis is not a distinct disease. Song YW, Kim SJ, Heo TH, Kim MH, Kim JB. Muscle Nerve; 2012 Dec 29; 46(6):914-6. PubMed ID: 22926674 [Abstract] [Full Text] [Related]