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Journal Abstract Search

191 related items for PubMed ID: 9453037

  • 1. [Hypokalemic periodic paralysis and ataxia--Ca channel disorders].
    Konishi T.
    No To Shinkei; 1997 Dec; 49(12):1068-78. PubMed ID: 9453037
    [No Abstract] [Full Text] [Related]

  • 2. [Hypokalemic periodic paralysis: new advances].
    Cattaneo FA.
    Schweiz Med Wochenschr; 1998 Feb 21; 128(8):297-301. PubMed ID: 9551533
    [Abstract] [Full Text] [Related]

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  • 5. Muscle fiber conduction velocity in arg1239his mutation in hypokalemic periodic paralysis.
    Links TP, van der Hoeven JH.
    Muscle Nerve; 2000 Feb 21; 23(2):296. PubMed ID: 10639629
    [No Abstract] [Full Text] [Related]

  • 6. Spinal anesthesia for a patient with a calcium channel mutation causing hypokalemic periodic paralysis.
    Hecht ML, Valtysson B, Hogan K.
    Anesth Analg; 1997 Feb 21; 84(2):461-4. PubMed ID: 9024050
    [No Abstract] [Full Text] [Related]

  • 7. Primary periodic paralyses.
    Finsterer J.
    Acta Neurol Scand; 2008 Mar 21; 117(3):145-58. PubMed ID: 18031562
    [Abstract] [Full Text] [Related]

  • 8. Sodium channel defects in myotonia and periodic paralysis.
    Cannon SC.
    Annu Rev Neurosci; 1996 Mar 21; 19():141-64. PubMed ID: 8833439
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  • 9. A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine.
    Alonso I, Barros J, Tuna A, Seixas A, Coutinho P, Sequeiros J, Silveira I.
    Clin Genet; 2004 Jan 21; 65(1):70-2. PubMed ID: 15032980
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  • 11. [Familial and thyrotoxic hypokalemic paralysis].
    Barthélemy M, Loiseau D, Liote F, Caquet R.
    Ann Med Interne (Paris); 1983 Jan 21; 134(6):573-80. PubMed ID: 6360010
    [No Abstract] [Full Text] [Related]

  • 12. [Physiopathology of hypokalemic familial paralysis].
    Kotsias BA.
    Medicina (B Aires); 1986 Jan 21; 46(4):461-6. PubMed ID: 3574109
    [No Abstract] [Full Text] [Related]

  • 13. [Electromyographic study of an induced attack in a case of hypokalemic familial periodic paralysis].
    Isch-Treussard C, Jésel M, Tempé D, Warter JM, Isch F.
    Rev Neurol (Paris); 1968 Jun 21; 118(6):543-5. PubMed ID: 5724665
    [No Abstract] [Full Text] [Related]

  • 14. 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 21; 42(3):305-12. PubMed ID: 9307251
    [Abstract] [Full Text] [Related]

  • 15. An expanding view for the molecular basis of familial periodic paralysis.
    Cannon SC.
    Neuromuscul Disord; 2002 Aug 21; 12(6):533-43. PubMed ID: 12117476
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  • 16. CACNA1A mutations: hemiplegic migraine, episodic ataxia type 2, and the others.
    Tournier-Lasserve E.
    Neurology; 1999 Jul 13; 53(1):3-4. PubMed ID: 10408526
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  • 18. Speculations on hypokalemic periodic paralysis.
    Zierler KL.
    Am J Med Sci; 1973 Aug 13; 266(2):130-3. PubMed ID: 4742367
    [No Abstract] [Full Text] [Related]

  • 19. [Molecular genetic findings in migraine].
    Østergaard E, Thomsen LL, Russell MB.
    Ugeskr Laeger; 2001 Nov 05; 163(45):6260-5. PubMed ID: 11723684
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  • 20. Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene.
    Hong D, Luan X, Chen B, Zheng R, Zhang W, Wang Z, Yuan Y.
    J Neurol Neurosurg Psychiatry; 2010 Jun 05; 81(6):703-4. PubMed ID: 20522878
    [No Abstract] [Full Text] [Related]

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