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Journal Abstract Search

134 related items for PubMed ID: 16836667

  • 21. [Relationships between age and accessory pathway location in Wolff-Parkinson-White syndrome].
    Huttin O, Brembilla-Perrot B.
    Ann Cardiol Angeiol (Paris); 2008 Aug; 57(4):225-30. PubMed ID: 18550025
    [Abstract] [Full Text] [Related]

  • 22. Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study.
    Brito D, Richard P, Komajda M, Madeira H.
    Rev Port Cardiol; 2008 Feb; 27(2):147-73. PubMed ID: 18488914
    [Abstract] [Full Text] [Related]

  • 23. [Wolff-Parkinson-White syndrome in Ebstein's anomaly].
    Torres PI.
    Arch Cardiol Mex; 2007 Feb; 77 Suppl 2():S2-37-S2-39. PubMed ID: 17972375
    [Abstract] [Full Text] [Related]

  • 24. Risk factors for atrioventricular tachycardia degenerating to atrial flutter/fibrillation in the young with Wolff-Parkinson-White.
    Harahsheh A, Du W, Singh H, Karpawich PP.
    Pacing Clin Electrophysiol; 2008 Oct; 31(10):1307-12. PubMed ID: 18811812
    [Abstract] [Full Text] [Related]

  • 25. Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family.
    van der Steld LP, Campuzano O, Pérez-Serra A, Moura de Barros Zamorano M, Sousa Matos S, Brugada R.
    Am J Case Rep; 2017 Jul 10; 18():766-776. PubMed ID: 28690312
    [Abstract] [Full Text] [Related]

  • 26. Clinical, electrocardiographic, and electrophysiologic characteristics of patients with a fasciculoventricular pathway: the role of PRKAG2 mutation.
    Sternick EB, Oliva A, Gerken LM, Magalhães L, Scarpelli R, Correia FS, Rego S, Santana O, Brugada R, Wellens HJ.
    Heart Rhythm; 2011 Jan 10; 8(1):58-64. PubMed ID: 20888928
    [Abstract] [Full Text] [Related]

  • 27. Association of congenital, diffuse electrical disease in children with normal heart: sick sinus syndrome, intraventricular conduction block, and monomorphic ventricular tachycardia.
    Iturralde-Torres P, Nava-Townsend S, Gómez-Flores J, Medeiros-Domingo A, Colín-Lizalde L, Hermosillo AG, Victoria D, Márquez MF.
    J Cardiovasc Electrophysiol; 2008 May 10; 19(5):550-5. PubMed ID: 17971134
    [Abstract] [Full Text] [Related]

  • 28. Molecular Pathogenesis of Familial Wolff-Parkinson-White Syndrome.
    Miyamoto L.
    J Med Invest; 2018 May 10; 65(1.2):1-8. PubMed ID: 29593177
    [Abstract] [Full Text] [Related]

  • 29. 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 10; 10(3):294-302. PubMed ID: 18308751
    [Abstract] [Full Text] [Related]

  • 30. Wolff-Parkinson-White syndrome in Patients With MELAS.
    Sproule DM, Kaufmann P, Engelstad K, Starc TJ, Hordof AJ, De Vivo DC.
    Arch Neurol; 2007 Nov 10; 64(11):1625-7. PubMed ID: 17998445
    [Abstract] [Full Text] [Related]

  • 31. Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
    Dalal D, James C, Devanagondi R, Tichnell C, Tucker A, Prakasa K, Spevak PJ, Bluemke DA, Abraham T, Russell SD, Calkins H, Judge DP.
    J Am Coll Cardiol; 2006 Oct 03; 48(7):1416-24. PubMed ID: 17010805
    [Abstract] [Full Text] [Related]

  • 32. Familial conduction system disease associated with hypertrophic cardiomyopathy.
    Bahl A, Saikia UN, Talwar KK.
    Int J Cardiol; 2008 Apr 25; 125(3):e44-7. PubMed ID: 17445920
    [Abstract] [Full Text] [Related]

  • 33. 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 25; 16(3):178-82. PubMed ID: 16487706
    [Abstract] [Full Text] [Related]

  • 34. Prevalence of hypertrophic cardiomyopathy in highly trained athletes: relevance to pre-participation screening.
    Basavarajaiah S, Wilson M, Whyte G, Shah A, McKenna W, Sharma S.
    J Am Coll Cardiol; 2008 Mar 11; 51(10):1033-9. PubMed ID: 18325444
    [Abstract] [Full Text] [Related]

  • 35. When Paying Attention Pays Back: Missense Mutation c.1006G>A p. (Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction Abnormalities in a Caucasian Patient: Case Report and Literature Review.
    Micaglio E, Tondi L, Benedetti S, Schiavo MA, Camporeale A, Disabato G, Attanasio A, Guida G, Carrafiello G, Piepoli M, Spagnolo P, Pappone C, Lombardi M.
    Int J Mol Sci; 2024 Aug 23; 25(17):. PubMed ID: 39273120
    [Abstract] [Full Text] [Related]

  • 36. WPW and preexcitation syndromes.
    Sethi KK, Dhall A, Chadha DS, Garg S, Malani SK, Mathew OP.
    J Assoc Physicians India; 2007 Apr 23; 55 Suppl():10-5. PubMed ID: 18368860
    [Abstract] [Full Text] [Related]

  • 37. The electrocardiogram in the patient with syncope.
    Dovgalyuk J, Holstege C, Mattu A, Brady WJ.
    Am J Emerg Med; 2007 Jul 23; 25(6):688-701. PubMed ID: 17606095
    [Abstract] [Full Text] [Related]

  • 38. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.
    Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, Ali Hassan AS, Ahmad F, Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R.
    N Engl J Med; 2001 Jun 14; 344(24):1823-31. PubMed ID: 11407343
    [Abstract] [Full Text] [Related]

  • 39. Atrial fibrillation in the Wolff-Parkinson-White syndrome: ECG recognition and treatment in the ED.
    Fengler BT, Brady WJ, Plautz CU.
    Am J Emerg Med; 2007 Jun 14; 25(5):576-83. PubMed ID: 17543664
    [Abstract] [Full Text] [Related]

  • 40. Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.
    Kubo T, Gimeno JR, Bahl A, Steffensen U, Steffensen M, Osman E, Thaman R, Mogensen J, Elliott PM, Doi Y, McKenna WJ.
    J Am Coll Cardiol; 2007 Jun 26; 49(25):2419-26. PubMed ID: 17599605
    [Abstract] [Full Text] [Related]

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