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Journal Abstract Search

296 related items for PubMed ID: 15221887

  • 21. A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis.
    Hirano M, Kokunai Y, Nagai A, Nakamura Y, Saigoh K, Kusunoki S, Takahashi MP.
    J Neurol Sci; 2011 Oct 15; 309(1-2):9-11. PubMed ID: 21855088
    [Abstract] [Full Text] [Related]

  • 22. Gender differences in penetrance and phenotype in hypokalemic periodic paralysis.
    Ke Q, Luo B, Qi M, Du Y, Wu W.
    Muscle Nerve; 2013 Jan 15; 47(1):41-5. PubMed ID: 23019082
    [Abstract] [Full Text] [Related]

  • 23. Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.
    Sternberg D, Maisonobe T, Jurkat-Rott K, Nicole S, Launay E, Chauveau D, Tabti N, Lehmann-Horn F, Hainque B, Fontaine B.
    Brain; 2001 Jun 15; 124(Pt 6):1091-9. PubMed ID: 11353725
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  • 27. A report of fulminant malignant hyperthermia in a patient with a novel mutation of the CACNA1S gene.
    Toppin PJ, Chandy TT, Ghanekar A, Kraeva N, Beattie WS, Riazi S.
    Can J Anaesth; 2010 Jul 15; 57(7):689-93. PubMed ID: 20431982
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  • 28. [From gene to diseases; hypokalemic periodic paralysis].
    Links TP, Ginjaar HB, van der Hoeven JH.
    Ned Tijdschr Geneeskd; 2004 May 22; 148(21):1035-8. PubMed ID: 15185439
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  • 30. Determination of a positive malignant hyperthermia (MH) disposition without the in vitro contracture test in families carrying the RYR1 Arg614Cys mutation.
    Rueffert H, Olthoff D, Deutrich C, Froster UG.
    Clin Genet; 2001 Aug 22; 60(2):117-24. PubMed ID: 11553045
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  • 31. [Ionic channel pathies].
    Yang T, Yao WX, Jiang MX.
    Sheng Li Ke Xue Jin Zhan; 1998 Jul 22; 29(3):239-42. PubMed ID: 12501643
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  • 32. Sodium channel gene mutations in hypokalemic periodic paralysis: an uncommon cause in the UK.
    Davies NP, Eunson LH, Samuel M, Hanna MG.
    Neurology; 2001 Oct 09; 57(7):1323-5. PubMed ID: 11591859
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  • 33. A fulminant malignant hyperthermia episode in a patient with ryanodine receptor gene mutation p.Tyr522Ser.
    Girard T, Suhner M, Levano S, Singer M, Zollinger A, Hofer CK.
    Anesth Analg; 2008 Dec 09; 107(6):1953-5. PubMed ID: 19020143
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  • 34. A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis.
    Dias Da Silva MR, Cerutti JM, Arnaldi LA, Maciel RM.
    J Clin Endocrinol Metab; 2002 Nov 09; 87(11):4881-4. PubMed ID: 12414843
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  • 36. Molecular basis of inherited calcium channelopathies: role of mutations in pore-forming subunits.
    McKeown L, Robinson P, Jones OT.
    Acta Pharmacol Sin; 2006 Jul 09; 27(7):799-812. PubMed ID: 16787562
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  • 37. Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause?
    Stunnenberg BC, Deinum J, Links TP, Wilde AA, Franssen H, Drost G.
    Muscle Nerve; 2014 Sep 09; 50(3):327-32. PubMed ID: 25088161
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  • 38. Novel ryanodine receptor mutation that may cause malignant hyperthermia.
    Kaufmann A, Kraft B, Michalek-Sauberer A, Weigl LG.
    Anesthesiology; 2008 Sep 09; 109(3):457-64. PubMed ID: 18719443
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  • 39. New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.
    Vicart S, Sternberg D, Fournier E, Ochsner F, Laforet P, Kuntzer T, Eymard B, Hainque B, Fontaine B.
    Neurology; 2004 Dec 14; 63(11):2120-7. PubMed ID: 15596759
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  • 40. [Malignant hyperthermia as a complication of anesthesia: predisposition is hereditary].
    Snoeck MM, Gielen MJ, Sengers RC, Padberg GW, Iles DE, Booij LH.
    Ned Tijdschr Geneeskd; 1997 Mar 29; 141(13):616-9. PubMed ID: 9190536
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