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 *

150 related articles for article (PubMed ID: 35576393)

  • 1. Congenital Long QT Syndrome: A Review of Genetic and Pathophysiologic Etiologies, Phenotypic Subtypes, and Clinical Management.
    Pandit M; Finn C; Tahir UA; Frishman WH
    Cardiol Rev; 2023 Nov-Dec 01; 31(6):318-324. PubMed ID: 35576393
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The genetic basis of long QT and short QT syndromes: a mutation update.
    Hedley PL; Jørgensen P; Schlamowitz S; Wangari R; Moolman-Smook J; Brink PA; Kanters JK; Corfield VA; Christiansen M
    Hum Mutat; 2009 Nov; 30(11):1486-511. PubMed ID: 19862833
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Epilepsy in patients with long QT syndrome type 1: A Norwegian family.
    González A; Aurlien D; Haugaa KH; Taubøll E
    Epilepsy Behav Case Rep; 2018; 10():118-121. PubMed ID: 30406014
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long-term proarrhythmic pharmacotherapy among patients with congenital long QT syndrome and risk of arrhythmia and mortality.
    Weeke PE; Kellemann JS; Jespersen CB; Theilade J; Kanters JK; Hansen MS; Christiansen M; Marstrand P; Gislason GH; Torp-Pedersen C; Bundgaard H; Jensen HK; Tfelt-Hansen J
    Eur Heart J; 2019 Oct; 40(37):3110-3117. PubMed ID: 31079148
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetics of long-QT syndrome.
    Nakano Y; Shimizu W
    J Hum Genet; 2016 Jan; 61(1):51-5. PubMed ID: 26108145
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The genetics underlying acquired long QT syndrome: impact for genetic screening.
    Itoh H; Crotti L; Aiba T; Spazzolini C; Denjoy I; Fressart V; Hayashi K; Nakajima T; Ohno S; Makiyama T; Wu J; Hasegawa K; Mastantuono E; Dagradi F; Pedrazzini M; Yamagishi M; Berthet M; Murakami Y; Shimizu W; Guicheney P; Schwartz PJ; Horie M
    Eur Heart J; 2016 May; 37(18):1456-64. PubMed ID: 26715165
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation and treatment of pediatric patients with congenital or acquired long QT interval syndromes.
    Phillips JR; Case CL
    Prog Pediatr Cardiol; 2001 Aug; 13(2):101-110. PubMed ID: 11457679
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.
    Itoh H; Sakaguchi T; Ding WG; Watanabe E; Watanabe I; Nishio Y; Makiyama T; Ohno S; Akao M; Higashi Y; Zenda N; Kubota T; Mori C; Okajima K; Haruna T; Miyamoto A; Kawamura M; Ishida K; Nagaoka I; Oka Y; Nakazawa Y; Yao T; Jo H; Sugimoto Y; Ashihara T; Hayashi H; Ito M; Imoto K; Matsuura H; Horie M
    Circ Arrhythm Electrophysiol; 2009 Oct; 2(5):511-23. PubMed ID: 19843919
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A recessive variant of the Romano-Ward long-QT syndrome?
    Priori SG; Schwartz PJ; Napolitano C; Bianchi L; Dennis A; De Fusco M; Brown AM; Casari G
    Circulation; 1998 Jun; 97(24):2420-5. PubMed ID: 9641694
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Jervell and Lange-Nielsen syndrome: homozygous missense mutation of KCNQ1 in a Turkish family.
    Bostan O; Temel ŞG; Cangül H; Archer CN; Çil E
    Pediatr Cardiol; 2013; 34(8):2063-7. PubMed ID: 23400408
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Computational Study on Effect of KCNQ1 P535T Mutation in a Cardiac Ventricular Tissue.
    Satish H; Machireddy RR
    J Membr Biol; 2023 Jun; 256(3):287-297. PubMed ID: 37166559
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
    Jongbloed RJ; Wilde AA; Geelen JL; Doevendans P; Schaap C; Van Langen I; van Tintelen JP; Cobben JM; Beaufort-Krol GC; Geraedts JP; Smeets HJ
    Hum Mutat; 1999; 13(4):301-10. PubMed ID: 10220144
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The heterogeneous spectrum of the long QT syndrome.
    Patel ND; Singh BK; Mathew ST
    Eur J Intern Med; 2006 Jul; 17(4):235-40. PubMed ID: 16762771
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic and clinical advances in congenital long QT syndrome.
    Mizusawa Y; Horie M; Wilde AA
    Circ J; 2014; 78(12):2827-33. PubMed ID: 25274057
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital and acquired long QT syndrome. Current concepts and management.
    Chiang CE
    Cardiol Rev; 2004; 12(4):222-34. PubMed ID: 15191637
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital Long QT syndrome and torsade de pointes.
    El-Sherif N; Turitto G; Boutjdir M
    Ann Noninvasive Electrocardiol; 2017 Nov; 22(6):. PubMed ID: 28670758
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular genetics of the long QT syndrome: clinical aspects].
    Sepp R; Csanády M
    Orv Hetil; 1999 Nov; 140(47):2633-8. PubMed ID: 10613047
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Long QT syndrome: ionic basis and arrhythmia mechanism in long QT syndrome type 1.
    Sanguinetti MC
    J Cardiovasc Electrophysiol; 2000 Jun; 11(6):710-2. PubMed ID: 10868746
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.