81 related articles for article (PubMed ID: 18071084)
21. Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death.
Mitchell RN; Ashar FN; Jarvelin MR; Froguel P; Sotoodehnia N; Brody JA; Sebert S; Huikuri H; Rioux J; Goyette P; Newcomb CE; Junttila MJ; Arking DE
J Am Heart Assoc; 2019 Dec; 8(23):e013751. PubMed ID: 31747862
[TBL] [Abstract][Full Text] [Related]
22. Oxidative Stress Induced Ventricular Arrhythmia and Impairment of Cardiac Function in Nos1ap Deleted Mice.
Sugiyama K; Sasano T; Kurokawa J; Takahashi K; Okamura T; Kato N; Isobe M; Furukawa T
Int Heart J; 2016 May; 57(3):341-9. PubMed ID: 27170476
[TBL] [Abstract][Full Text] [Related]
23. A NOS1AP gene variant is associated with a paradoxical increase of the QT-interval shortening effect of digoxin.
Soroush N; Aarnoudse AJ; Kavousi M; Kors JA; Ikram MA; Newton-Cheh C; Ahmadizar F; Stricker BH
Pharmacogenomics J; 2022 Feb; 22(1):55-61. PubMed ID: 34616002
[TBL] [Abstract][Full Text] [Related]
24. Do patients with long QT syndrome remain at risk for sudden cardiac death after 40 years of age?
Postema PG; Wilde AA
Nat Clin Pract Cardiovasc Med; 2008 Oct; 5(10):602-3. PubMed ID: 18665134
[TBL] [Abstract][Full Text] [Related]
25. Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish.
Post W; Shen H; Damcott C; Arking DE; Kao WH; Sack PA; Ryan KA; Chakravarti A; Mitchell BD; Shuldiner AR
Hum Hered; 2007; 64(4):214-9. PubMed ID: 17565224
[TBL] [Abstract][Full Text] [Related]
26. Epilepsy and the long QT syndrome: is there a link?--Commentary on Hindocha et al.
Stramba-Badiale M
Epilepsia; 2008 Feb; 49(2):366. PubMed ID: 18251841
[No Abstract] [Full Text] [Related]
27. Inducible over-expression of cardiac Nos1ap causes short QT syndrome in transgenic mice.
Jänsch M; Lubomirov LT; Trum M; Williams T; Schmitt J; Schuh K; Qadri F; Maier LS; Bader M; Ritter O
FEBS Open Bio; 2023 Jan; 13(1):118-132. PubMed ID: 36352324
[TBL] [Abstract][Full Text] [Related]
28. Genetic variation in the NOS1AP gene is associated with the incidence of diabetes mellitus in users of calcium channel blockers.
Becker ML; Visser LE; Newton-Cheh C; Witteman JC; Hofman A; Uitterlinden AG; Stricker BH
Diabetologia; 2008 Nov; 51(11):2138-40. PubMed ID: 18766325
[No Abstract] [Full Text] [Related]
29. Cardiac arrhythmias and SUDEP--Commentary on Hindocha et al.
Cooper PN
Epilepsia; 2008 Feb; 49(2):366-7. PubMed ID: 18251840
[No Abstract] [Full Text] [Related]
30. Subclinical hypothyroidism is characterized by increased QT interval dispersion among women.
Bakiner O; Ertorer ME; Haydardedeoglu FE; Bozkirli E; Tutuncu NB; Demirag NG
Med Princ Pract; 2008; 17(5):390-4. PubMed ID: 18685279
[TBL] [Abstract][Full Text] [Related]
31. DNA structural variants as genetic risk factors for the long QT syndrome.
Rich SS; Hall IM
J Am Coll Cardiol; 2011 Jan; 57(1):48-50. PubMed ID: 21185500
[No Abstract] [Full Text] [Related]
32. The corrected QT interval before and after heart transplantation.
Moore JP; Alejos JC; Perens G; Wong S; Shannon KM
Am J Cardiol; 2009 Aug; 104(4):596-601. PubMed ID: 19660618
[TBL] [Abstract][Full Text] [Related]
33. Congenital long-QT syndromes: who's at risk for sudden cardiac death?
Berul CI
Circulation; 2008 Apr; 117(17):2178-80. PubMed ID: 18443247
[No Abstract] [Full Text] [Related]
34. Psychotropic drugs associated with corrected QT interval prolongation.
van Noord C; Straus SM; Sturkenboom MC; Hofman A; Aarnoudse AJ; Bagnardi V; Kors JA; Newton-Cheh C; Witteman JC; Stricker BH
J Clin Psychopharmacol; 2009 Feb; 29(1):9-15. PubMed ID: 19142100
[TBL] [Abstract][Full Text] [Related]
35. A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
Ikrar T; Hanawa H; Watanabe H; Okada S; Aizawa Y; Ramadan MM; Komura S; Yamashita F; Chinushi M; Aizawa Y
J Cardiovasc Electrophysiol; 2008 May; 19(5):541-9. PubMed ID: 18266681
[TBL] [Abstract][Full Text] [Related]
36. Corrigendum: Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.
Kozyrev SV; Abelson AK; Wojcik J; Zaghlool A; Linga Reddy MP; Sanchez E; Gunnarsson I; Svenungsson E; Sturfelt G; Jönsen A; Truedsson L; Pons-Estel BA; Witte T; D'Alfonso S; Barrizzone N; Danieli MG; Gutierrez C; Suarez A; Junker P; Laustrup H; Francisca González-Escribano M; Martin J; Abderrahim H; Alarcón-Riquelme ME
Nat Genet; 2008 Apr; 40(4):484. PubMed ID: 18368128
[No Abstract] [Full Text] [Related]
37. Long QT Syndrome.
Goldenberg I; Zareba W; Moss AJ
Curr Probl Cardiol; 2008 Nov; 33(11):629-94. PubMed ID: 18835466
[TBL] [Abstract][Full Text] [Related]
38. Relation of increased short-term variability of QT interval to congenital long-QT syndrome.
Hinterseer M; Beckmann BM; Thomsen MB; Pfeufer A; Dalla Pozza R; Loeff M; Netz H; Steinbeck G; Vos MA; Kääb S
Am J Cardiol; 2009 May; 103(9):1244-8. PubMed ID: 19406266
[TBL] [Abstract][Full Text] [Related]
39. Cardiac muscle-restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features.
Smith A; Auer D; Johnson M; Sanchez E; Ross H; Ward C; Chakravarti A; Kapoor A
G3 (Bethesda); 2023 Nov; 13(11):. PubMed ID: 37708408
[TBL] [Abstract][Full Text] [Related]
40. Sudden cardiac death: The larger problem... The larger genome.
Spooner PM
J Cardiovasc Electrophysiol; 2009 May; 20(5):585-96. PubMed ID: 19207788
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
