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Journal Abstract Search

134 related items for PubMed ID: 16836667

  • 1. 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; 17(7):724-32. PubMed ID: 16836667
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  • 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
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  • 4. [Same genotype and different phenotypes in a family with PRKAG2 gene mutation].
    Hong K, Oliva A, Cheng XS, Brugada P, Brugada J, Sternick EB, Brugada R.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2007 Jun 10; 35(6):552-4. PubMed ID: 17711718
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  • 5. 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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  • 6. 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 27; 9(8):597-600. PubMed ID: 17483151
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  • 9. Nodoventricular accessory pathways in PRKAG2-dependent familial preexcitation syndrome reveal a disorder in cardiac development.
    Tan HL, van der Wal AC, Campian ME, Kruyswijk HH, ten Hove Jansen B, van Doorn DJ, Oskam HJ, Becker AE, Wilde AA.
    Circ Arrhythm Electrophysiol; 2008 Oct 27; 1(4):276-81. PubMed ID: 19808419
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  • 11. 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
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  • 13. Coexistence of the Wolff-Parkinson-White preexcitation syndrome and complete atrioventricular block.
    Johnson CD.
    Bol Asoc Med P R; 2007 Dec 18; 99(3):263-9. PubMed ID: 19610584
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  • 15. Pseudo myocardial infarction and pseudo ventricular hypertrophy ECG patterns in Wolff-Parkinson-White syndrome.
    Khan IA, Shaw IS.
    Am J Emerg Med; 2000 Nov 18; 18(7):802-6. PubMed ID: 11103732
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  • 16. [A familial form of conduction defects associated with a PRKAG2 gene mutation].
    Pochmalicki G, Genest M, Richard P, Komajda M, Charron P.
    Arch Mal Coeur Vaiss; 2007 Sep 18; 100(9):760-5. PubMed ID: 18033003
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  • 17. 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 18; 15(2):267-276. PubMed ID: 28917552
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  • 18. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 18; 56(3):105-52. PubMed ID: 19728970
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  • 20. Familial Wolff-Parkinson-White syndrome is linked to the loci on chromosome 7q3.
    Liu W, Liu G, Hu D, Qi Y, Shan Z, Yang D, Liu D, Wang Y.
    Chin Med J (Engl); 2002 Nov 18; 115(11):1733-5. PubMed ID: 12609097
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