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159 related items for PubMed ID: 16686673

  • 1. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction?
    Light PE.
    J Cardiovasc Electrophysiol; 2006 May; 17 Suppl 1():S158-S161. PubMed ID: 16686673
    [Abstract] [Full Text] [Related]

  • 2. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.
    Arad M, Moskowitz IP, Patel VV, Ahmad F, Perez-Atayde AR, Sawyer DB, Walter M, Li GH, Burgon PG, Maguire CT, Stapleton D, Schmitt JP, Guo XX, Pizard A, Kupershmidt S, Roden DM, Berul CI, Seidman CE, Seidman JG.
    Circulation; 2003 Jun 10; 107(22):2850-6. PubMed ID: 12782567
    [Abstract] [Full Text] [Related]

  • 3. Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy.
    Arad M, Benson DW, Perez-Atayde AR, McKenna WJ, Sparks EA, Kanter RJ, McGarry K, Seidman JG, Seidman CE.
    J Clin Invest; 2002 Feb 10; 109(3):357-62. PubMed ID: 11827995
    [Abstract] [Full Text] [Related]

  • 4. Mathematical simulations of the effects of altered AMP-kinase activity on I and the action potential in rat ventricle.
    Bazzazi H, Clark RB, Giles WR.
    J Cardiovasc Electrophysiol; 2006 May 10; 17 Suppl 1():S162-S168. PubMed ID: 16686674
    [Abstract] [Full Text] [Related]

  • 5. High risk of sudden death associated with a PRKAG2-related familial Wolff-Parkinson-White syndrome.
    Zhang LP, Hui B, Gao BR.
    J Electrocardiol; 2011 May 10; 44(4):483-6. PubMed ID: 20381067
    [Abstract] [Full Text] [Related]

  • 6. Familial pseudo-Wolff-Parkinson-White syndrome.
    Sternick EB, Oliva A, Magalhães LP, Gerken LM, Hong K, Santana O, Brugada P, Brugada J, Brugada R.
    J Cardiovasc Electrophysiol; 2006 Jul 10; 17(7):724-32. PubMed ID: 16836667
    [Abstract] [Full Text] [Related]

  • 7. Distinct early signaling events resulting from the expression of the PRKAG2 R302Q mutant of AMPK contribute to increased myocardial glycogen.
    Folmes KD, Chan AY, Koonen DP, Pulinilkunnil TC, Baczkó I, Hunter BE, Thorn S, Allard MF, Roberts R, Gollob MH, Light PE, Dyck JR.
    Circ Cardiovasc Genet; 2009 Oct 10; 2(5):457-66. PubMed ID: 20031621
    [Abstract] [Full Text] [Related]

  • 8. Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy.
    Gollob MH, Seger JJ, Gollob TN, Tapscott T, Gonzales O, Bachinski L, Roberts R.
    Circulation; 2001 Dec 18; 104(25):3030-3. PubMed ID: 11748095
    [Abstract] [Full Text] [Related]

  • 9. Regulation of ion channels and arrhythmias in the ischemic heart.
    Akar JG, Akar FG.
    J Electrocardiol; 2007 Dec 18; 40(6 Suppl):S37-41. PubMed ID: 17993326
    [Abstract] [Full Text] [Related]

  • 10. [Genetic aspects of the etiology of arrhythmia].
    Thierfelder L.
    Z Kardiol; 2000 Dec 18; 89 Suppl 3():1-5. PubMed ID: 10810779
    [Abstract] [Full Text] [Related]

  • 11. Genetic mutations and arrhythmia: simulation from DNA to electrocardiogram.
    Zhu ZI, Clancy CE.
    J Electrocardiol; 2007 Dec 18; 40(6 Suppl):S47-50. PubMed ID: 17993328
    [Abstract] [Full Text] [Related]

  • 12. Mechanisms for the genesis of paroxysmal atrial fibrillation in the Wolff Parkinson-White syndrome: intrinsic atrial muscle vulnerability vs. electrophysiological properties of the accessory pathway.
    Centurión OA, Shimizu A, Isomoto S, Konoe A.
    Europace; 2008 Mar 18; 10(3):294-302. PubMed ID: 18308751
    [Abstract] [Full Text] [Related]

  • 13. Molecular Pathogenesis of Familial Wolff-Parkinson-White Syndrome.
    Miyamoto L.
    J Med Invest; 2018 Mar 18; 65(1.2):1-8. PubMed ID: 29593177
    [Abstract] [Full Text] [Related]

  • 14. Transgenic mouse model of ventricular preexcitation and atrioventricular reentrant tachycardia induced by an AMP-activated protein kinase loss-of-function mutation responsible for Wolff-Parkinson-White syndrome.
    Sidhu JS, Rajawat YS, Rami TG, Gollob MH, Wang Z, Yuan R, Marian AJ, DeMayo FJ, Weilbacher D, Taffet GE, Davies JK, Carling D, Khoury DS, Roberts R.
    Circulation; 2005 Jan 04; 111(1):21-9. PubMed ID: 15611370
    [Abstract] [Full Text] [Related]

  • 15. Atrial vulnerability is a major mechanism of paroxysmal atrial fibrillation in patients with Wolff-Parkinson-White syndrome.
    Zhang Y, Wang L.
    Med Hypotheses; 2006 Jan 04; 67(6):1345-7. PubMed ID: 16697118
    [Abstract] [Full Text] [Related]

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  • 17. A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis.
    Laforêt P, Richard P, Said MA, Romero NB, Lacene E, Leroy JP, Baussan C, Hogrel JY, Lavergne T, Wahbi K, Hainque B, Duboc D.
    Neuromuscul Disord; 2006 Mar 04; 16(3):178-82. PubMed ID: 16487706
    [Abstract] [Full Text] [Related]

  • 18. CRISPR correction of the PRKAG2 gene mutation in the patient's induced pluripotent stem cell-derived cardiomyocytes eliminates electrophysiological and structural abnormalities.
    Ben Jehuda R, Eisen B, Shemer Y, Mekies LN, Szantai A, Reiter I, Cui H, Guan K, Haron-Khun S, Freimark D, Sperling SR, Gherghiceanu M, Arad M, Binah O.
    Heart Rhythm; 2018 Feb 04; 15(2):267-276. PubMed ID: 28917552
    [Abstract] [Full Text] [Related]

  • 19. WPW and preexcitation syndromes.
    Sethi KK, Dhall A, Chadha DS, Garg S, Malani SK, Mathew OP.
    J Assoc Physicians India; 2007 Apr 04; 55 Suppl():10-5. PubMed ID: 18368860
    [Abstract] [Full Text] [Related]

  • 20. A familial form of conduction defect related to a mutation in the PRKAG2 gene.
    Charron P, Genest M, Richard P, Komajda M, Pochmalicki G.
    Europace; 2007 Aug 04; 9(8):597-600. PubMed ID: 17483151
    [Abstract] [Full Text] [Related]

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