725 related articles for article (PubMed ID: 10483966)
1. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
Swan H; Viitasalo M; Piippo K; Laitinen P; Kontula K; Toivonen L
J Am Coll Cardiol; 1999 Sep; 34(3):823-9. PubMed ID: 10483966
[TBL] [Abstract][Full Text] [Related]
2. Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
Zareba W; Moss AJ; Locati EH; Lehmann MH; Peterson DR; Hall WJ; Schwartz PJ; Vincent GM; Priori SG; Benhorin J; Towbin JA; Robinson JL; Andrews ML; Napolitano C; Timothy K; Zhang L; Medina A;
J Am Coll Cardiol; 2003 Jul; 42(1):103-9. PubMed ID: 12849668
[TBL] [Abstract][Full Text] [Related]
3. Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.
Inoue M; Shimizu M; Ino H; Yamaguchi M; Terai H; Hayashi K; Kiyama M; Sakata K; Hayashi T; Mabuchi H
Circ J; 2003 Jun; 67(6):495-8. PubMed ID: 12808265
[TBL] [Abstract][Full Text] [Related]
4. Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations.
Lupoglazoff JM; Denjoy I; Berthet M; Neyroud N; Demay L; Richard P; Hainque B; Vaksmann G; Klug D; Leenhardt A; Maillard G; Coumel P; Guicheney P
Circulation; 2001 Feb; 103(8):1095-101. PubMed ID: 11222472
[TBL] [Abstract][Full Text] [Related]
5. The long QT syndrome: new diagnostic and therapeutic approach in the era of molecular biology.
Priori SG; Cantù F; Schwartz PJ
Schweiz Med Wochenschr; 1996 Oct; 126(41):1727-31. PubMed ID: 8893413
[TBL] [Abstract][Full Text] [Related]
6. Genotype- and mutation site-specific QT adaptation during exercise, recovery, and postural changes in children with long-QT syndrome.
Aziz PF; Wieand TS; Ganley J; Henderson J; Patel AR; Iyer VR; Vogel RL; McBride M; Vetter VL; Shah MJ
Circ Arrhythm Electrophysiol; 2011 Dec; 4(6):867-73. PubMed ID: 21956039
[TBL] [Abstract][Full Text] [Related]
7. Multi-undulant T-U-wave, sinus bradycardia and long QT syndrome: a possible phenotype of mutant genes controlling the inward potassium rectifiers.
Shen CT; Wu YC; Yu SS; Wang NK
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(4):267-75. PubMed ID: 9297927
[TBL] [Abstract][Full Text] [Related]
8. The long QT syndromes: genetic basis and clinical implications.
Chiang CE; Roden DM
J Am Coll Cardiol; 2000 Jul; 36(1):1-12. PubMed ID: 10898405
[TBL] [Abstract][Full Text] [Related]
9. Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.
Wong JA; Gula LJ; Klein GJ; Yee R; Skanes AC; Krahn AD
Circ Arrhythm Electrophysiol; 2010 Apr; 3(2):120-5. PubMed ID: 20071715
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q
Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)].
Lupoglazoff JM; Denjoy I; Berthet M; Hainque B; Vaksmann G; Klug D; Villain E; Lucet V; Guicheney P; Coumel P
Arch Mal Coeur Vaiss; 2001 May; 94(5):470-8. PubMed ID: 11434015
[TBL] [Abstract][Full Text] [Related]
14. A new oral therapy for long QT syndrome: long-term oral potassium improves repolarization in patients with HERG mutations.
Etheridge SP; Compton SJ; Tristani-Firouzi M; Mason JW
J Am Coll Cardiol; 2003 Nov; 42(10):1777-82. PubMed ID: 14642687
[TBL] [Abstract][Full Text] [Related]
15. C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
Berthet M; Denjoy I; Donger C; Demay L; Hammoude H; Klug D; Schulze-Bahr E; Richard P; Funke H; Schwartz K; Coumel P; Hainque B; Guicheney P
Circulation; 1999 Mar; 99(11):1464-70. PubMed ID: 10086971
[TBL] [Abstract][Full Text] [Related]
16. Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1).
Wilde AA; Jongbloed RJ; Doevendans PA; Düren DR; Hauer RN; van Langen IM; van Tintelen JP; Smeets HJ; Meyer H; Geelen JL
J Am Coll Cardiol; 1999 Feb; 33(2):327-32. PubMed ID: 9973011
[TBL] [Abstract][Full Text] [Related]
17. Epinephrine bolus test in detecting long QT syndrome mutation carriers with indeterminable electrocardiographic phenotype.
Hekkala AM; Swan H; Viitasalo M; Väänänen H; Toivonen L
Ann Noninvasive Electrocardiol; 2011 Apr; 16(2):172-9. PubMed ID: 21496168
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Long QT syndrome in children: the value of rate corrected QT interval and DNA analysis as screening tests in the general population.
Allan WC; Timothy K; Vincent GM; Palomaki GE; Neveux LM; Haddow JE
J Med Screen; 2001; 8(4):173-7. PubMed ID: 11743032
[TBL] [Abstract][Full Text] [Related]
20. The inherited long QT syndrome: from ion channel to bedside.
Vincent GM; Timothy K; Fox J; Zhang L
Cardiol Rev; 1999; 7(1):44-55. PubMed ID: 10348966
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]