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 *

153 related articles for article (PubMed ID: 17876385)

  • 1. Molecular autopsy in the sudden cardiac death of a young woman: a first Canadian report.
    Rutberg J; Green MS; Gow RM; Geraghty MT; Honeywell C; Ewen J; Birnie DH; Tang A; Lemery R; Gollob MH
    Can J Cardiol; 2007 Sep; 23(11):904-6. PubMed ID: 17876385
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
    Winkel BG; Larsen MK; Berge KE; Leren TP; Nissen PH; Olesen MS; Hollegaard MV; Jespersen T; Yuan L; Nielsen N; Haunsø S; Svendsen JH; Wang Y; Kristensen IB; Jensen HK; Tfelt-Hansen J; Banner J
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1092-8. PubMed ID: 22882672
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Post-mortem genetic testing in a family with long-QT syndrome and hypertrophic cardiomyopathy.
    Kane DA; Triedman J
    Cardiovasc Pathol; 2014; 23(2):107-9. PubMed ID: 24322056
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Posthumous diagnosis of long QT syndrome from neonatal screening cards.
    Gladding PA; Evans CA; Crawford J; Chung SK; Vaughan A; Webster D; Neas K; Love DR; Rees MI; Shelling AN; Skinner JR
    Heart Rhythm; 2010 Apr; 7(4):481-6. PubMed ID: 20167303
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the SCN5A gene: evidence for a link between long QT syndrome and sudden death?
    Kiehne N; Kauferstein S
    Forensic Sci Int Genet; 2007 Jun; 1(2):170-4. PubMed ID: 19083750
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular autopsy for sudden unexplained death? Time to discuss pros and cons.
    Mazzanti A; Priori SG
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1099-102. PubMed ID: 22966897
    [No Abstract]   [Full Text] [Related]  

  • 7. Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.
    Tester DJ; Medeiros-Domingo A; Will ML; Haglund CM; Ackerman MJ
    Mayo Clin Proc; 2012 Jun; 87(6):524-39. PubMed ID: 22677073
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family.
    Zamorano-León JJ; Alonso-Orgaz S; Moreno J; Cinza R; García-Torrent MJ; Pérez-Castellano N; Pérez-Villacastín J; Macaya C; López-Farré AJ
    Int J Cardiol; 2010 Jul; 142(2):206-8. PubMed ID: 19136169
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
    Chang YS; Yang YW; Lin YN; Lin KH; Chang KC; Chang JG
    Int Heart J; 2015; 56(4):450-3. PubMed ID: 26118593
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Aborted Cardiac Arrest in LQT2 Related to Novel
    Bileišienė N; Barysienė J; Mikštienė V; Preikšaitienė E; Marinskis G; Keževičiūtė M; Utkus A; Aidietis A
    Medicina (Kaunas); 2021 Jul; 57(7):. PubMed ID: 34357002
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Long QT syndrome mutation detection by SNaPshot technique.
    Edelmann J; Schumann S; Nastainczyk M; Husser-Bollmann D; Lessig R
    Int J Legal Med; 2012 Nov; 126(6):969-73. PubMed ID: 21769575
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Long QT and Brugada syndrome gene mutations in New Zealand.
    Chung SK; MacCormick JM; McCulley CH; Crawford J; Eddy CA; Mitchell EA; Shelling AN; French JK; Skinner JR; Rees MI
    Heart Rhythm; 2007 Oct; 4(10):1306-14. PubMed ID: 17905336
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM
    Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
    [TBL] [Abstract][Full Text] [Related]  

  • 14. KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
    Crotti L; Lundquist AL; Insolia R; Pedrazzini M; Ferrandi C; De Ferrari GM; Vicentini A; Yang P; Roden DM; George AL; Schwartz PJ
    Circulation; 2005 Aug; 112(9):1251-8. PubMed ID: 16116052
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Investigation of ion channel gene variants in patients with long QT syndrome.
    Ernesto C; Cruz FE; Lima FS; Coutinho JL; Silva R; Urményi TP; Carvalho AC; Rondinelli E
    Arq Bras Cardiol; 2011 Mar; 96(3):172-8. PubMed ID: 21308345
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular genetic basis of sudden cardiac death.
    Towbin JA
    Pediatr Clin North Am; 2004 Oct; 51(5):1229-55. PubMed ID: 15331282
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Postmortem molecular screening in unexplained sudden death.
    Chugh SS; Senashova O; Watts A; Tran PT; Zhou Z; Gong Q; Titus JL; Hayflick SJ
    J Am Coll Cardiol; 2004 May; 43(9):1625-9. PubMed ID: 15120823
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family.
    Ichikawa M; Ohno S; Fujii Y; Ozawa J; Sonoda K; Fukuyama M; Kato K; Kimura H; Itoh H; Hayashi H; Horie M
    Intern Med; 2016; 55(3):259-62. PubMed ID: 26831020
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of potassium ion channel genes in sudden death cases among patients administered psychotropic drug therapy: are polymorphisms in LQT genes a potential risk factor?
    Kamei S; Sato N; Harayama Y; Nunotani M; Takatsu K; Shiozaki T; Hayashi T; Asamura H
    J Hum Genet; 2014 Feb; 59(2):95-9. PubMed ID: 24284363
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Long QT molecular autopsy in sudden infant death syndrome.
    Glengarry JM; Crawford J; Morrow PL; Stables SR; Love DR; Skinner JR
    Arch Dis Child; 2014 Jul; 99(7):635-40. PubMed ID: 24596401
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.