These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


113 related items for PubMed ID: 12501643

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Mutation analysis of two patients with hypokalemic periodic paralysis and suspected malignant hyperthermia.
    Marchant CL, Ellis FR, Halsall PJ, Hopkins PM, Robinson RL.
    Muscle Nerve; 2004 Jul; 30(1):114-7. PubMed ID: 15221887
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Getting a charge out of periodic paralysis?
    Cannon SC.
    Neurology; 2009 May 05; 72(18):1540-1. PubMed ID: 19414720
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [A family with heat-sensitive myotonia alternating with hypokalemic periodic paralysis].
    Aoki T, Sugiura Y, Sugiyama Y, Ogata M, Hida C, Honma M, Yamamoto T.
    Rinsho Shinkeigaku; 2000 Apr 05; 40(4):358-63. PubMed ID: 10967653
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. [Familial hypokalemic periodic paralysis].
    Nemoto H, Kurihara T.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr 05; (35):144-7. PubMed ID: 11555894
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Mutation screening in Korean hypokalemic periodic paralysis patients: a novel SCN4A Arg672Cys mutation.
    Kim MK, Lee SH, Park MS, Kim BC, Cho KH, Lee MC, Kim JH, Kim SM.
    Neuromuscul Disord; 2004 Nov 05; 14(11):727-31. PubMed ID: 15482957
    [Abstract] [Full Text] [Related]

  • 13. Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family.
    Incecik F, Hergüner MO, Altunbaşak S, Lehman-Horn F.
    Turk J Pediatr; 2010 Nov 05; 52(4):409-10. PubMed ID: 21043388
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Gating pore current in an inherited ion channelopathy.
    Sokolov S, Scheuer T, Catterall WA.
    Nature; 2007 Mar 01; 446(7131):76-8. PubMed ID: 17330043
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [Mutations in the heart's pacemaker channels--a new cause of sick sinus node syndrome and long-QT syndrome].
    Vitved T, Lianee HT, Støvring B, Sigurd BM, Christiansen M.
    Ugeskr Laeger; 2008 Mar 10; 170(11):929-33. PubMed ID: 18397618
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Ion channels--basic science and clinical disease.
    Ackerman MJ, Clapham DE.
    N Engl J Med; 1997 May 29; 336(22):1575-86. PubMed ID: 9164815
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 6.