BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 7721491)

  • 41. The Jervell and Lange-Nielsen syndrome; atrial pacing combined with ß-blocker therapy, a favorable approach in young high-risk patients with long QT syndrome?
    Früh A; Siem G; Holmström H; Døhlen G; Haugaa KH
    Heart Rhythm; 2016 Nov; 13(11):2186-2192. PubMed ID: 27451284
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Congenital hearing loss in Jervell and Lange-Nielsen syndrome.
    Jacobson J; Jacobson C; Francis P
    J Am Acad Audiol; 1990 Jul; 1(3):171-3. PubMed ID: 1721555
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Jervell and Lange-Nielson Syndrome masquerading as intractable epilepsy.
    Goyal JP; Sethi A; Shah VB
    Ann Indian Acad Neurol; 2012 Apr; 15(2):145-7. PubMed ID: 22566733
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Molecular biology and the prolonged QT syndromes.
    Towbin JA; Vatta M
    Am J Med; 2001 Apr; 110(5):385-98. PubMed ID: 11286954
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Cardiac tachyarrhythmias in hereditary long QT syndromes presenting as a seizure disorder.
    Sundaram MB; McMeekin JD; Gulamhusein S
    Can J Neurol Sci; 1986 Aug; 13(3):262-3. PubMed ID: 3742343
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [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]  

  • 47. [The idiopathic QT syndrome as the cause of epileptic and nonepileptic seizures].
    Hördt M; Haverkamp W; Oberwittler C; Lüdemann P; Borggrefe M; Ringelstein EB; Breithardt G
    Nervenarzt; 1995 Apr; 66(4):282-7. PubMed ID: 7783815
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Picture of the month. Jervell and Lange-Nielsen syndrome (long QT syndrome).
    Narchi H; Tunnessen WW
    Arch Pediatr Adolesc Med; 1999 Apr; 153(4):425-6. PubMed ID: 10201729
    [No Abstract]   [Full Text] [Related]  

  • 49. Prolonged QT syndrome in children: an uncommon but potentially fatal entity.
    Friedman MJ; Mull CC; Sharieff GQ; Tsarouhas N
    J Emerg Med; 2003 Feb; 24(2):173-9. PubMed ID: 12609648
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Jervell and Lange-Nielsen syndrome in Norwegian children: aspects around cochlear implantation, hearing, and balance.
    Siem G; Früh A; Leren TP; Heimdal K; Teig E; Harris S
    Ear Hear; 2008 Apr; 29(2):261-9. PubMed ID: 18595190
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Jervell-Lange Nielsen syndrome in a family with the long QT syndrome (LQTS).
    Shanbag P
    Indian J Pediatr; 2007 Jan; 74(1):90; author reply 90. PubMed ID: 17264466
    [No Abstract]   [Full Text] [Related]  

  • 52. Autosomal Recessive Long QT Syndrome: Clinical Aspects and Therapy.
    Righi D; Porco L; Di Mambro C; Gnazzo M; Baban A; Paglia S; Silvetti MS; Novelli A; Tozzi AE; Drago F
    Pediatr Cardiol; 2023 Dec; 44(8):1736-1740. PubMed ID: 37597120
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.
    Wang Z; Li H; Moss AJ; Robinson J; Zareba W; Knilans T; Bowles NE; Towbin JA
    Mol Genet Metab; 2002 Apr; 75(4):308-16. PubMed ID: 12051962
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Cochlear Implantation in Congenital Long-QT Syndrome: A Comprehensive Study.
    Anto R; Maheswari S; Vadivu S; Kameswaran M
    J Int Adv Otol; 2019 Dec; 15(3):352-357. PubMed ID: 31846911
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Novel frameshift mutation in the
    Amirian A; Dalili SM; Zafari Z; Saber S; Karimipoor M; Akbari V; Fazelifar AF; Zeinali S
    Iran J Basic Med Sci; 2018 Jan; 21(1):108-111. PubMed ID: 29372044
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [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]  

  • 57. The combined novel KCNQ1 frameshift I145Sfs*92 and nonsense W392X variants caused Jervell and Lange-Nielsen syndrome in a Chinese infant presenting with sustained foetal bradycardia.
    Zhang Y; Li X; Yang Y; Wang J; Gao X; Fan M
    Europace; 2020 Dec; 22(12):1880-1884. PubMed ID: 32830254
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene.
    Kılıç E; Ertuğrul İ; Özer S; Alikaşifoğlu M; Aktaş D; Boduroğlu K; Ütine GE
    Turk J Pediatr; 2014; 56(5):542-5. PubMed ID: 26022593
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Heterozygous mutation in KCNQ1 cause Jervell and Lange-Nielsen syndrome].
    Liu WL; Hu DY; Li P; Li CL; Qin XG; Li YT; Li L; Li ZM; Dong W; Qi Y; Wang Q
    Zhonghua Xin Xue Guan Bing Za Zhi; 2005 Jan; 33(1):41-4. PubMed ID: 15924777
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Genotype-phenotype analysis of three Chinese families with Jervell and Lange-Nielsen syndrome.
    Gao Y; Li C; Liu W; Wu R; Qiu X; Liang R; Li L; Zhang L; Hu D
    J Cardiovasc Dis Res; 2012 Apr; 3(2):67-75. PubMed ID: 22629021
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.