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 *

152 related articles for article (PubMed ID: 37597120)

  • 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. [Jervell and Lange-Nielsen syndrome].
    Zhang WJ; Sun Y; Kong WJ
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Sep; 33(9):825-829. PubMed ID: 31446697
    [No Abstract]   [Full Text] [Related]  

  • 43. Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness.
    Oertli A; Rinné S; Moss R; Kääb S; Seemann G; Beckmann BM; Decher N
    Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33498651
    [No Abstract]   [Full Text] [Related]  

  • 44. Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.
    Sieliwonczyk E; Alaerts M; Simons E; Snyders D; Nijak A; Vandendriessche B; Schepers D; Akdeniz D; Van Craenenbroeck E; Knaepen K; Rabaut L; Heidbuchel H; Van Laer L; Saenen J; Labro AJ; Loeys B
    Orphanet J Rare Dis; 2023 Jan; 18(1):23. PubMed ID: 36721196
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [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]  

  • 46. Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome.
    Hobbs JB; Peterson DR; Moss AJ; McNitt S; Zareba W; Goldenberg I; Qi M; Robinson JL; Sauer AJ; Ackerman MJ; Benhorin J; Kaufman ES; Locati EH; Napolitano C; Priori SG; Towbin JA; Vincent GM; Zhang L
    JAMA; 2006 Sep; 296(10):1249-54. PubMed ID: 16968849
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. 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]  

  • 49. Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome.
    Chang Q; Wang J; Li Q; Kim Y; Zhou B; Wang Y; Li H; Lin X
    EMBO Mol Med; 2015 Aug; 7(8):1077-86. PubMed ID: 26084842
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome
    Rinné S; Oertli A; Nagel C; Tomsits P; Jenewein T; Kääb S; Kauferstein S; Loewe A; Beckmann BM; Decher N
    Int J Mol Sci; 2023 Jan; 24(2):. PubMed ID: 36674868
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation.
    Barsheshet A; Moss AJ; McNitt S; Polonsky S; Lopes CM; Zareba W; Robinson JL; Ackerman MJ; Benhorin J; Kaufman ES; Towbin JA; Vincent GM; Qi M; Goldenberg I
    Circ Cardiovasc Genet; 2011 Oct; 4(5):491-9. PubMed ID: 21831960
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Mexiletine Shortens the QT Interval in Patients With Potassium Channel-Mediated Type 2 Long QT Syndrome.
    Bos JM; Crotti L; Rohatgi RK; Castelletti S; Dagradi F; Schwartz PJ; Ackerman MJ
    Circ Arrhythm Electrophysiol; 2019 May; 12(5):e007280. PubMed ID: 31006312
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [The long-term efficacy of left cardiac sympathetic denervation in long QT syndrome].
    Li X; Li CL; Liu YG; Liu JY; Wang JF; Li ZM; Ma DY; Hu D
    Zhonghua Xin Xue Guan Bing Za Zhi; 2022 Jun; 50(6):556-562. PubMed ID: 35705464
    [No Abstract]   [Full Text] [Related]  

  • 54. Large deletion in KCNQ1 identified in a family with Jervell and Lange-Nielsen syndrome.
    Sung JY; Bae EJ; Park S; Kim SY; Hyun YJ; Park SS; Seong MW
    Ann Lab Med; 2014 Sep; 34(5):395-8. PubMed ID: 25187895
    [TBL] [Abstract][Full Text] [Related]  

  • 55. New KCNQ1 c.604+1G>C variant associated with Jervell-Lange Nielsen syndrome in homozygosity and compound heterozygosity.
    Arana-Rueda E; Pezzotti MR; Pedrote A; Marcos-Fuentes L; Frutos-López M; Castellano A
    Rev Esp Cardiol (Engl Ed); 2022 Jun; 75(6):529-531. PubMed ID: 35144896
    [No Abstract]   [Full Text] [Related]  

  • 56. Sodium channel blockers in the management of long QT syndrome types 3 and 2: A system review and meta-analysis.
    Yang Y; Lv TT; Li SY; Zhang P
    J Cardiovasc Electrophysiol; 2021 Nov; 32(11):3057-3067. PubMed ID: 34427958
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A case of Long QT syndrome type 3 aggravated by beta-blockers and alleviated by mexiletine: the role of epinephrine provocation test.
    Park J; Kim SK; Pak HN
    Yonsei Med J; 2013 Mar; 54(2):529-33. PubMed ID: 23364992
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Treatment on arrhythmia electric storm in a Jervell and Lange-Nielsen syndrome patient by ablation of the triggering premature ventricular contraction: a case report.
    Zhang R; Ding C; Wang H
    Ann Palliat Med; 2021 Apr; 10(4):4938-4943. PubMed ID: 33040543
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics.
    Piippo K; Swan H; Pasternack M; Chapman H; Paavonen K; Viitasalo M; Toivonen L; Kontula K
    J Am Coll Cardiol; 2001 Feb; 37(2):562-8. PubMed ID: 11216980
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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]  

    [Previous]   [Next]    [New Search]
    of 8.