These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 2188546)

  • 1. [Congenital sensorineural deafness and associated syndromes].
    Moatti L; Garabedian EN; Lacombe H; Spir-Jacob C
    Ann Otolaryngol Chir Cervicofac; 1990; 107(3):181-6. PubMed ID: 2188546
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Long QT syndrome in children with congenital deafness.
    Sathyamurthy I; Jayanthi K; Dash J; Srinivasan KN
    Indian Pediatr; 2009 Jun; 46(6):507-8. PubMed ID: 19213984
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.
    Neyroud N; Tesson F; Denjoy I; Leibovici M; Donger C; Barhanin J; Fauré S; Gary F; Coumel P; Petit C; Schwartz K; Guicheney P
    Nat Genet; 1997 Feb; 15(2):186-9. PubMed ID: 9020846
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Rare etiologies of congenital deafness].
    Hélias J; Pacalon J; Lafon JC
    Arch Fr Pediatr; 1985; 42(7):503-6. PubMed ID: 4083970
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [KCNQ 1 (KvLQT1) missense mutation causing congenital long QT syndrome (Jervell-Lange-Nielsen) in a Mexican family].
    Márquez MF; Ramos-Kuri M; Hernández-Pacheco G; Estrada J; Fabregat JR; Pérez-Vielma N; Gómez-Flores J; González-Hermosillo A; Cárdenas M; Vargas-Alarcón G
    Arch Cardiol Mex; 2006; 76(3):257-62. PubMed ID: 17091796
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X.
    Wei J; Fish FA; Myerburg RJ; Roden DM; George AL
    Hum Mutat; 2000 Apr; 15(4):387-8. PubMed ID: 10737999
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Jervell and Lange-Nielsen cardioauditory syndrome].
    Ferreira M das G; da Cunha GP; Marçallo FA
    Arq Bras Cardiol; 1986 Sep; 47(3):173-9. PubMed ID: 3593016
    [No Abstract]   [Full Text] [Related]  

  • 8. Cochlear implantation in patients with Jervell and Lange-Nielsen syndrome, and a review of literature.
    Yanmei F; Yaqin W; Haibo S; Huiqun Z; Zhengnong C; Dongzhen Y; Shankai Y
    Int J Pediatr Otorhinolaryngol; 2008 Nov; 72(11):1723-9. PubMed ID: 18805595
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Niikawa-Kuroki (Kabuki) syndrome with congenital sensorineural deafness: evidence for a wide spectrum of inner ear abnormalities.
    Tekin M; Fitoz S; Arici S; Cetinkaya E; Incesulu A
    Int J Pediatr Otorhinolaryngol; 2006 May; 70(5):885-9. PubMed ID: 16325926
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inner ear histopathology in genetically determined congenital deafness.
    Lindsay JR
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):21-32. PubMed ID: 5173349
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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
    [No Abstract]   [Full Text] [Related]  

  • 12. [The Jervell- and Lange-Nielsen syndrome. A peculiar form of hereditary cardio-myopathy].
    Athanasiou DJ; Weiner C
    Munch Med Wochenschr; 1972 Apr; 114(15):698-706. PubMed ID: 5068323
    [No Abstract]   [Full Text] [Related]  

  • 13. The Jervell and Lange-Nielsen syndrome.
    Cusimano F; Martines E; Rizzo C
    Int J Pediatr Otorhinolaryngol; 1991 Jul; 22(1):49-58. PubMed ID: 1917338
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Electrocardiographic changes following exercise in the congenitally deaf school children: relationship with Jervell Lange Neilsen syndrome (the Long QT syndrome).
    Srivastava RD; Pramod J; Deep J; Jaison TM; Singh S; Soni K
    Indian J Physiol Pharmacol; 1998 Oct; 42(4):515-20. PubMed ID: 10874353
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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
    [No Abstract]   [Full Text] [Related]  

  • 16. [Jervell and Lange-Nielsen syndrome. Cardiologic study of 211 deaf-mutes].
    Puletti M; Jacobellis GF; Borghi F
    Cuore Circ; 1967 Dec; 51(6):251-61. PubMed ID: 5617374
    [No Abstract]   [Full Text] [Related]  

  • 17. Cochlear implantation in children with congenital long QT syndrome: Introduction of an evidence-based pathway of care.
    Scott-Warren V; Bendon A; Bruce IA; Henderson L; Diacono J
    Cochlear Implants Int; 2018 Nov; 19(6):350-354. PubMed ID: 30227792
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sensorineural deafness in the FG syndrome: report on four new cases.
    Neri G; Blumberg B; Miles PV; Opitz JM
    Am J Med Genet; 1984 Oct; 19(2):369-77. PubMed ID: 6542310
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 98(2-3):319-27. PubMed ID: 19027783
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Phenotypic variability in Townes-Brocks syndrome.
    Monteiro de Pina-Neto J
    Am J Med Genet; 1984 May; 18(1):147-52. PubMed ID: 6741990
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.