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Journal Abstract Search

136 related items for PubMed ID: 19808419

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  • 2. [Electrophysiologic findings and high frequency catheter ablation in atriofascicular and nodoventricular pathways ("Mahaim bundles")].
    Kottkamp H, Chen X, Hindricks G, Willems S, Haverkamp W, Wichter T, Breithardt G, Borggrefe M.
    Z Kardiol; 1995; 84 Suppl 2():153-62. PubMed ID: 7571779
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  • 3. Glycogen storage diseases presenting as hypertrophic cardiomyopathy.
    Arad M, Maron BJ, Gorham JM, Johnson WH, Saul JP, Perez-Atayde AR, Spirito P, Wright GB, Kanter RJ, Seidman CE, Seidman JG.
    N Engl J Med; 2005 Jan 27; 352(4):362-72. PubMed ID: 15673802
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  • 4. 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
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  • 6. A rare connection: fasciculoventricular pathway in PRKAG2 disease.
    Govindan M, Ward D, Behr E.
    J Cardiovasc Electrophysiol; 2010 Mar 10; 21(3):329-32. PubMed ID: 19732236
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  • 7. Cardiovascular magnetic resonance findings in patients with PRKAG2 gene mutations.
    Pöyhönen P, Hiippala A, Ollila L, Kaasalainen T, Hänninen H, Heliö T, Tallila J, Vasilescu C, Kivistö S, Ojala T, Holmström M.
    J Cardiovasc Magn Reson; 2015 Oct 24; 17():89. PubMed ID: 26496977
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  • 8. 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 24; 2(5):457-66. PubMed ID: 20031621
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  • 9. 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 24; 17(7):724-32. PubMed ID: 16836667
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  • 13. Identification of a novel de novo mutation associated with PRKAG2 cardiac syndrome and early onset of heart failure.
    Liu Y, Bai R, Wang L, Zhang C, Zhao R, Wan D, Chen X, Caceres G, Barr D, Barajas-Martinez H, Antzelevitch C, Hu D.
    PLoS One; 2013 Jul 24; 8(5):e64603. PubMed ID: 23741347
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  • 14. Electrophysiological and histopathological characteristics of progressive atrioventricular block accompanied by familial dilated cardiomyopathy caused by a novel mutation of lamin A/C gene.
    Otomo J, Kure S, Shiba T, Karibe A, Shinozaki T, Yagi T, Naganuma H, Tezuka F, Miura M, Ito M, Watanabe J, Matsubara Y, Shirato K.
    J Cardiovasc Electrophysiol; 2005 Feb 24; 16(2):137-45. PubMed ID: 15720451
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  • 19. Short atrioventricular Mahaim fibers: observations on their clinical, electrocardiographic, and electrophysiologic profile.
    Sternick EB, Fagundes ML, Cruz FE, Timmermans C, Sosa EA, Rodriguez LM, Gerken LM, Scanavacca MI, Wellens HJ.
    J Cardiovasc Electrophysiol; 2005 Feb 24; 16(2):127-34. PubMed ID: 15720449
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