198 related articles for article (PubMed ID: 23465283)
21. A mitochondrial DNA polymorphism associated with cardiac arrhythmia investigated in sudden infant death syndrome.
Arnestad M; Opdal SH; Vege A; Rognum TO
Acta Paediatr; 2007 Feb; 96(2):206-10. PubMed ID: 17429906
[TBL] [Abstract][Full Text] [Related]
22. Infant sudden death: Mutations responsible for impaired Nav1.5 channel trafficking and function.
Gando I; Morganstein J; Jana K; McDonald TV; Tang Y; Coetzee WA
Pacing Clin Electrophysiol; 2017 Jun; 40(6):703-712. PubMed ID: 28370132
[TBL] [Abstract][Full Text] [Related]
23. Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome.
Van Norstrand DW; Tester DJ; Ackerman MJ
Heart Rhythm; 2008 May; 5(5):712-5. PubMed ID: 18452875
[TBL] [Abstract][Full Text] [Related]
24. Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
Van Driest SL; Wells QS; Stallings S; Bush WS; Gordon A; Nickerson DA; Kim JH; Crosslin DR; Jarvik GP; Carrell DS; Ralston JD; Larson EB; Bielinski SJ; Olson JE; Ye Z; Kullo IJ; Abul-Husn NS; Scott SA; Bottinger E; Almoguera B; Connolly J; Chiavacci R; Hakonarson H; Rasmussen-Torvik LJ; Pan V; Persell SD; Smith M; Chisholm RL; Kitchner TE; He MM; Brilliant MH; Wallace JR; Doheny KF; Shoemaker MB; Li R; Manolio TA; Callis TE; Macaya D; Williams MS; Carey D; Kapplinger JD; Ackerman MJ; Ritchie MD; Denny JC; Roden DM
JAMA; 2016 Jan; 315(1):47-57. PubMed ID: 26746457
[TBL] [Abstract][Full Text] [Related]
25. Functional characterization of a novel hERG variant in a family with recurrent sudden infant death syndrome: Retracting a genetic diagnosis.
Sergeev V; Perry F; Roston TM; Sanatani S; Tibbits GF; Claydon TW
Forensic Sci Int; 2018 Mar; 284():39-45. PubMed ID: 29331839
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
Christiansen M; Hedley PL; Theilade J; Stoevring B; Leren TP; Eschen O; Sørensen KM; Tybjærg-Hansen A; Ousager LB; Pedersen LN; Frikke-Schmidt R; Aidt FH; Hansen MG; Hansen J; Bloch Thomsen PE; Toft E; Henriksen FL; Bundgaard H; Jensen HK; Kanters JK
BMC Med Genet; 2014 Mar; 15():31. PubMed ID: 24606995
[TBL] [Abstract][Full Text] [Related]
28. Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia.
Son MK; Ki CS; Park SJ; Huh J; Kim JS; On YK
J Korean Med Sci; 2013 Jul; 28(7):1021-6. PubMed ID: 23853484
[TBL] [Abstract][Full Text] [Related]
29. Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome.
Christiansen M; Tønder N; Larsen LA; Andersen PS; Simonsen H; Oyen N; Kanters JK; Jacobsen JR; Fosdal I; Wettrell G; Kjeldsen K
Am J Cardiol; 2005 Feb; 95(3):433-4. PubMed ID: 15670565
[TBL] [Abstract][Full Text] [Related]
30. The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote.
Hedley PL; Kanters JK; Dembic M; Jespersen T; Skibsbye L; Aidt FH; Eschen O; Graff C; Behr ER; Schlamowitz S; Corfield V; McKenna WJ; Christiansen M
Circ Cardiovasc Genet; 2013 Oct; 6(5):452-61. PubMed ID: 24021552
[TBL] [Abstract][Full Text] [Related]
31. The role of the sodium current complex in a nonreferred nationwide cohort of sudden infant death syndrome.
Winkel BG; Yuan L; Olesen MS; Sadjadieh G; Wang Y; Risgaard B; Jabbari R; Haunsø S; Holst AG; Hollegaard MV; Tfelt-Hansen J; Jespersen T
Heart Rhythm; 2015 Jun; 12(6):1241-9. PubMed ID: 25757662
[TBL] [Abstract][Full Text] [Related]
32. Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.
Hayashi K; Konno T; Tada H; Tani S; Liu L; Fujino N; Nohara A; Hodatsu A; Tsuda T; Tanaka Y; Kawashiri MA; Ino H; Makita N; Yamagishi M
Circ Arrhythm Electrophysiol; 2015 Oct; 8(5):1095-104. PubMed ID: 26129877
[TBL] [Abstract][Full Text] [Related]
33. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
Antzelevitch C
J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
[TBL] [Abstract][Full Text] [Related]
34. The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WT.
Mechakra A; Vincent Y; Chevalier P; Millat G; Ficker E; Jastrzebski M; Poulin H; Pouliot V; Chahine M; Christé G
Gene; 2014 Feb; 536(2):348-56. PubMed ID: 24334129
[TBL] [Abstract][Full Text] [Related]
35. Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
Tester DJ; Wong LCH; Chanana P; Gray B; Jaye A; Evans JM; Evans M; Fleming P; Jeffrey I; Cohen M; Tfelt-Hansen J; Simpson MA; Behr ER; Ackerman MJ
J Pediatr; 2018 Dec; 203():423-428.e11. PubMed ID: 30268395
[TBL] [Abstract][Full Text] [Related]
36. New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia.
Jabbari J; Jabbari R; Nielsen MW; Holst AG; Nielsen JB; Haunsø S; Tfelt-Hansen J; Svendsen JH; Olesen MS
Circ Cardiovasc Genet; 2013 Oct; 6(5):481-9. PubMed ID: 24025405
[TBL] [Abstract][Full Text] [Related]
37. Common variants in cardiac ion channel genes are associated with sudden cardiac death.
Albert CM; MacRae CA; Chasman DI; VanDenburgh M; Buring JE; Manson JE; Cook NR; Newton-Cheh C
Circ Arrhythm Electrophysiol; 2010 Jun; 3(3):222-9. PubMed ID: 20400777
[TBL] [Abstract][Full Text] [Related]
38. Genetic variants in eleven central and peripheral chemoreceptor genes in sudden infant death syndrome.
Neubauer J; Forst AL; Warth R; Both CP; Haas C; Thomas J
Pediatr Res; 2022 Oct; 92(4):1026-1033. PubMed ID: 35102300
[TBL] [Abstract][Full Text] [Related]
39. Long QT syndrome-associated mutations in intrauterine fetal death.
Crotti L; Tester DJ; White WM; Bartos DC; Insolia R; Besana A; Kunic JD; Will ML; Velasco EJ; Bair JJ; Ghidoni A; Cetin I; Van Dyke DL; Wick MJ; Brost B; Delisle BP; Facchinetti F; George AL; Schwartz PJ; Ackerman MJ
JAMA; 2013 Apr; 309(14):1473-82. PubMed ID: 23571586
[TBL] [Abstract][Full Text] [Related]
40. Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review.
Evans A; Bagnall RD; Duflou J; Semsarian C
Hum Pathol; 2013 Sep; 44(9):1730-6. PubMed ID: 23623143
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]