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PUBMED FOR HANDHELDS

Journal Abstract Search


98 related items for PubMed ID: 921112

  • 1. [Jervell-Lange-Nielsen syndrome. 13 year-course of 2 familial cases].
    Vacheron A, Heulin A, Vanetti A, Fidelle J, Frezal J, di Matteo J.
    Ann Med Interne (Paris); 1977; 128(6-7):553-6. PubMed ID: 921112
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  • 4. [Six cases of Jervell and Lange-Nielsen syndrome-epidemiological study of 8 schools for the deaf (author's transl)].
    Kawano M, Ishida K, Yabuki S, Seki K.
    Kokyu To Junkan; 1981 May; 29(5):553-62. PubMed ID: 7313359
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  • 11. [Additional observations on the Jervell and Lange-Nielsen syndrome].
    Athanasiou DJ, Müller-Seydlitz PM.
    Munch Med Wochenschr; 1972 Nov 10; 114(45):1961-5. PubMed ID: 4678445
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  • 12. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome.
    Bhuiyan ZA, Momenah TS, Amin AS, Al-Khadra AS, Alders M, Wilde AA, Mannens MM.
    Prog Biophys Mol Biol; 2008 Nov 10; 98(2-3):319-27. PubMed ID: 19027783
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  • 13. [Jervell and Lange-Nielsen syndrome. Cardiomegalic form and genetic myocardiopathies].
    Gillet B, Voegtlin R.
    Ann Cardiol Angeiol (Paris); 1973 Nov 10; 22(6):535-9. PubMed ID: 4772266
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  • 17. [Syncope attacks with lengthening of the Q-T interval, without deafness. 2 further cases of the Romano-Ward syndrome].
    Ambrosioni G, Lombardi G, Gaglioppa F, Pogiali I.
    Minerva Pediatr; 1975 Jun 23; 27(22):1247-54. PubMed ID: 1143211
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  • 19. [Re-entry mechanism of ventricular tachycardias in inhomogenic repolarization. With special reference to Jervell-Lange-Nielsen syndrome and similar states and their therapy].
    Theisen K, Jahrmärker H.
    Dtsch Med Wochenschr; 1975 May 16; 100(20):1141-7. PubMed ID: 1092539
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  • 20. [Congenital sensorineural deafness and associated syndromes].
    Moatti L, Garabedian EN, Lacombe H, Spir-Jacob C.
    Ann Otolaryngol Chir Cervicofac; 1990 May 16; 107(3):181-6. PubMed ID: 2188546
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