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425 related items for PubMed ID: 9561886

  • 1. Familial atrial septal defect with atrioventricular conduction defects.
    Mandorla S, Martino C.
    G Ital Cardiol; 1998 Mar; 28(3):294-6. PubMed ID: 9561886
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  • 2. Autosomal dominant atrial septal defect of ostium secundum type. Report of three families.
    Li Volti S, Distefano G, Garozzo R, Romeo MG, Sciacca P, Mollica F.
    Ann Genet; 1991 Mar; 34(1):14-8. PubMed ID: 1952784
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  • 3. 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 Mar; 44(1):69-72. PubMed ID: 11858385
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  • 4. [Familial forms of interauricular communication of the ostium secundum type].
    Thomas D, Lascault G, Caille B, Drobinski G, Huberman JP, Shqueir A, Grosgogeat Y.
    Arch Mal Coeur Vaiss; 1985 Aug; 78(8):1205-9. PubMed ID: 3935078
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  • 5. [Secundum atrial septal defect with prolonged atrioventricular conduction: an autosomal dominant hereditary cardiac defect (author's transl)].
    Schaede A, Ramacher J.
    Dtsch Med Wochenschr; 1977 Oct 28; 102(43):1552-4. PubMed ID: 913295
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  • 6. Familial atrial septal defect with prolonged atrioventricular conduction.
    Pease WE, Nordenberg A, Ladda RL.
    Circulation; 1976 May 28; 53(5):759-62. PubMed ID: 1260978
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  • 7. Familial atrial septal defect with prolonged atrioventricular conduction.
    Bosi G, Sensi A, Calzolari E, Scorrano M.
    Am J Med Genet; 1992 Jun 01; 43(3):641. PubMed ID: 1605267
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  • 11. [Pre- and postoperative study of arrhythmia in atrial septal defects (ostium secundum and sinus venosus)].
    Mycinski C, Fauchier JP, Cosnay P, Chantepie A, Marchand M, Moquet B, Huguet RG, Guillou L.
    Arch Mal Coeur Vaiss; 1988 May 01; 81(5):685-92. PubMed ID: 3136731
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  • 13. Atrioventricular nodal dysfunction in patients with atrial septal defect. Abnormalities of conduction and reciprocal rhythms.
    Sobrino JA, de Lombera F, del Rio A, Plaza I, Maté I, Sotillo JL, Hernández-Lanchas C, Sobrino N.
    Chest; 1982 Apr 01; 81(4):477-82. PubMed ID: 7067514
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  • 17. Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.
    Rifai L, Maazouzi W, Sefiani A.
    Cardiol Young; 2007 Feb 01; 17(1):107-9. PubMed ID: 17184575
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  • 20. [Atrial septal defect of the ostium secundum associated with incomplete left bundle branch block].
    Volpi A, Ferrario G, Dubini D, Maggi A, Rovelli GE, Parenti GF.
    G Ital Cardiol; 1983 Feb 01; 13(6):472-4. PubMed ID: 6642113
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