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PUBMED FOR HANDHELDS

Journal Abstract Search

109 related items for PubMed ID: 6865881

  • 41. [Familial sudden death in preexcitation syndrome. Surgical interruption of the anomalous pathways in two brothers (author's transl)].
    Critelli G, Gallagher JJ, Sealy WC, Lanza GG, Condorelli M.
    G Ital Cardiol; 1981; 11(12):1883-94. PubMed ID: 7346292
    [Abstract] [Full Text] [Related]

  • 42. [Clinical and genetic heterogeneity of cardiopathies with heart rhythm disorders in children].
    Ternova TI, Bochkova DN.
    Vopr Okhr Materin Det; 1978 May; 23(5):5-8. PubMed ID: 664520
    [No Abstract] [Full Text] [Related]

  • 43. [The use of xylocaine in cardiac arrhythmias associated with conduction disorders].
    Pellegrino L, Casari A, De Filippi R, Salerno J.
    Boll Soc Ital Cardiol; 1970 May; 15(6):665-70. PubMed ID: 5517661
    [No Abstract] [Full Text] [Related]

  • 44. Anorexia nervosa and second-degree atrioventricular block (Type I).
    Bravender T, Kanter R, Zucker N.
    Int J Eat Disord; 2006 Nov; 39(7):612-5. PubMed ID: 16937388
    [Abstract] [Full Text] [Related]

  • 45. A case of familial atrioventricular heart block affected by alteration of the autonomic nervous system.
    Takehara N, Kawamura Y, Sato N, Sato A, Kakuchi H, Kikuchi K.
    J Electrocardiol; 2001 Oct; 34(4):339-44. PubMed ID: 11590576
    [Abstract] [Full Text] [Related]

  • 46. Does an overlap syndrome really exist between Brugada syndrome and progressive cardiac conduction defect (Lenegre syndrome)?
    Shimizu W.
    J Cardiovasc Electrophysiol; 2006 Mar; 17(3):276-8. PubMed ID: 16643400
    [No Abstract] [Full Text] [Related]

  • 47. [Electrocardiographic changes in central nervous system diseases (cerebral T wave). Clinical study of 20 cases].
    Foyé R, Vallazza M, Locreille A, Videla J, Chiozza MA, Suarez LD, Suárez LD.
    Medicina (B Aires); 1981 Mar; 41(4):407-18. PubMed ID: 7339430
    [No Abstract] [Full Text] [Related]

  • 48. [Analysis of the frequency of cardiac arrhythmias and conduction disturbances from a health-care perspective].
    Vázquez Ruiz de Castroviejo E, Muñoz Bellido J, Lozano Cabezas C, Ramírez Moreno A, Guzmán Herrera M, Tarabini Castellani A, Fajardo Pineda A, Jiménez Araque B, Armenteros Lechuga JB, Pagola Vilardebó C.
    Rev Esp Cardiol; 2005 Jun; 58(6):657-65. PubMed ID: 15970121
    [Abstract] [Full Text] [Related]

  • 49. ["Supernormal" A-V conduction during chaotic atrial rhythm. A case report].
    Oreto G, Luzza F, Mangano A.
    G Ital Cardiol; 1983 Jun; 13(3):192-6. PubMed ID: 6884659
    [Abstract] [Full Text] [Related]

  • 50. Indications for permanent cardiac pacing.
    Alpert MA.
    Am Fam Physician; 1982 Jul; 26(1):187-97. PubMed ID: 7090963
    [No Abstract] [Full Text] [Related]

  • 51. Persistent partial atrial standstill with atrial dissociation and junctional rhythm.
    Cotoi S, Carasca E, Repolski M.
    Med Interne; 1982 Jul; 20(3):209-13. PubMed ID: 7156816
    [No Abstract] [Full Text] [Related]

  • 52. [Effective intracavitary pacemaking for Taxus baccata-induced cardiac conduction defects and arrhythmias].
    Łukasik-Głebocka M, Sieńko A, Klimaszyk D, Mańkowski W.
    Przegl Lek; 2007 Jul; 64(4-5):298-300. PubMed ID: 17724890
    [Abstract] [Full Text] [Related]

  • 53. A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression.
    Bundgaard H, Jøns C, Lodder EM, Izarzugaza JMG, Romero Herrera JA, Pehrson S, Tfelt-Hansen J, Ahlberg G, Olesen MS, Holst AG, Wellens H, de Villiers C, Hastings R, Stuart G, Brunak S, Wilde AAM, Watkins H, Christensen AH.
    N Engl J Med; 2018 Nov 01; 379(18):1780-1781. PubMed ID: 30380381
    [No Abstract] [Full Text] [Related]

  • 54. Progressive familial heart block (type I). A follow-up study after 10 years.
    Van der Merwe PL, Weymar HW, Torrington M, Brink AJ.
    S Afr Med J; 1988 Mar 05; 73(5):275-6. PubMed ID: 3347879
    [Abstract] [Full Text] [Related]

  • 55. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
    van Tintelen JP, Hofstra RM, Katerberg H, Rossenbacker T, Wiesfeld AC, du Marchie Sarvaas GJ, Wilde AA, van Langen IM, Nannenberg EA, van der Kooi AJ, Kraak M, van Gelder IC, van Veldhuisen DJ, Vos Y, van den Berg MP, Working Group on Inherited Cardiac Disorders, line 27/50, Interuniversity Cardiology Institute of The Netherlands.
    Am Heart J; 2007 Dec 05; 154(6):1130-9. PubMed ID: 18035086
    [Abstract] [Full Text] [Related]

  • 56. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
    Jakobs PM, Hanson EL, Crispell KA, Toy W, Keegan H, Schilling K, Icenogle TB, Litt M, Hershberger RE.
    J Card Fail; 2001 Sep 05; 7(3):249-56. PubMed ID: 11561226
    [Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58. Familial secundum atrial septal defect with dysrhythmia associated with web neck.
    Kiliç Z, Uçar B, Baş F, Dinleyici EC, Sari E.
    Turk J Pediatr; 2002 Sep 05; 44(1):69-72. PubMed ID: 11858385
    [Abstract] [Full Text] [Related]

  • 59. Short QT Syndrome: a familial cause of sudden death.
    Gaita F, Giustetto C, Bianchi F, Wolpert C, Schimpf R, Riccardi R, Grossi S, Richiardi E, Borggrefe M.
    Circulation; 2003 Aug 26; 108(8):965-70. PubMed ID: 12925462
    [Abstract] [Full Text] [Related]

  • 60. Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p.Asp187Tyr mutation in the GSN gene.
    Chastan N, Baert-Desurmont S, Saugier-Veber P, Dérumeaux G, Cabot A, Frébourg T, Hannequin D.
    Muscle Nerve; 2006 Jan 26; 33(1):113-9. PubMed ID: 16258946
    [Abstract] [Full Text] [Related]

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