164 related articles for article (PubMed ID: 12891885)
1. [Sudden fainting in a young woman].
Capaert S
Rev Med Brux; 2003 Jun; 24(3):176-8. PubMed ID: 12891885
[TBL] [Abstract][Full Text] [Related]
2. [Congenital long QT-syndrome: the cause of recurrent syncope and sudden death at a young age].
Akkerhuis JM; Baars HF; Marcelis CL; Akkerhuis KM; Wilde AA
Ned Tijdschr Geneeskd; 2007 Oct; 151(43):2357-64. PubMed ID: 18019210
[TBL] [Abstract][Full Text] [Related]
3. Idiopathic long q-t syndrome: brief case report and discussion.
Noble WE; Chaudhuri P; Qazi MA
W V Med J; 1994 Apr; 90(4):143-4. PubMed ID: 8009871
[TBL] [Abstract][Full Text] [Related]
4. Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.
Thomas D; Wimmer AB; Karle CA; Licka M; Alter M; Khalil M; Ulmer HE; Kathöfer S; Kiehn J; Katus HA; Schoels W; Koenen M; Zehelein J
Cardiovasc Res; 2005 Aug; 67(3):487-97. PubMed ID: 15950200
[TBL] [Abstract][Full Text] [Related]
5. [Long QT syndrome].
Watanabe A; Nakamura K; Morita H; Kusano KF; Ohe T
Nihon Rinsho; 2005 Jul; 63(7):1171-7. PubMed ID: 16001778
[TBL] [Abstract][Full Text] [Related]
6. [Polymorphic familial incessant ventricular rhythm disorders with ventricular repolarization abnormalities: borderline form of the congenital long QT syndrome?].
Leclercq JF; Maisonblanche P; Cauchemez B; Attuel P; Coumel P
Arch Mal Coeur Vaiss; 1984 Sep; 77(9):1013-9. PubMed ID: 6435576
[TBL] [Abstract][Full Text] [Related]
7. Syncope and sudden arrhythmic death complicating pregnancy. A case report of Romano-Ward syndrome.
McCurdy CM; Rutherford SE; Coddington CC
J Reprod Med; 1993 Mar; 38(3):233-4. PubMed ID: 8098062
[TBL] [Abstract][Full Text] [Related]
8. Jervell and Lange-Nielsen syndrome in a father and daughter from a large highly inbred family: a 16-year follow-up of 59 living members.
Sanyal SK; Kaul KK; Hussein A; Wilroy RS; Agarwal K; Sohel S
Cardiol Young; 2013 Aug; 23(4):530-9. PubMed ID: 23668803
[TBL] [Abstract][Full Text] [Related]
9. Congenital long QT syndromes: clinical features, molecular genetics and genetic testing.
Ching CK; Tan EC
Expert Rev Mol Diagn; 2006 May; 6(3):365-74. PubMed ID: 16706739
[TBL] [Abstract][Full Text] [Related]
10. An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome.
Bhuiyan ZA; Momenah TS; Amin AS; Al-Khadra AS; Alders M; Wilde AA; Mannens MM
Prog Biophys Mol Biol; 2008; 98(2-3):319-27. PubMed ID: 19027783
[TBL] [Abstract][Full Text] [Related]
11. [Familial long QT-syncope syndrome. 2 cases of Romano-Ward syndrome].
Pony JC; Mattheyses M; Daubert JC; Fourdilis M; Gouffault J
Arch Mal Coeur Vaiss; 1977 Oct; 70(10):1105-14. PubMed ID: 413520
[TBL] [Abstract][Full Text] [Related]
12. [KCNQ 1 (KvLQT1) missense mutation causing congenital long QT syndrome (Jervell-Lange-Nielsen) in a Mexican family].
Márquez MF; Ramos-Kuri M; Hernández-Pacheco G; Estrada J; Fabregat JR; Pérez-Vielma N; Gómez-Flores J; González-Hermosillo A; Cárdenas M; Vargas-Alarcón G
Arch Cardiol Mex; 2006; 76(3):257-62. PubMed ID: 17091796
[TBL] [Abstract][Full Text] [Related]
13. Romano-Ward syndrome: case report, family study and signal averaged electrocardiogram.
Rode P; Stajer D; Horvat M; Rakovec P; Milcinski M; Tomazic M
Cor Vasa; 1990; 32(4):335-42. PubMed ID: 2225883
[TBL] [Abstract][Full Text] [Related]
14. The homozygous KCNQ1 gene mutation associated with recessive Romano-Ward syndrome.
Novotny T; Kadlecova J; Janousek J; Gaillyova R; Bittnerova A; Florianova A; Sisakova M; Toman O; Chroust K; Papousek I; Spinar J
Pacing Clin Electrophysiol; 2006 Sep; 29(9):1013-5. PubMed ID: 16981927
[TBL] [Abstract][Full Text] [Related]
15. Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndrome.
Goldenberg I; Moss AJ; Zareba W; McNitt S; Robinson JL; Qi M; Towbin JA; Ackerman MJ; Murphy L
J Cardiovasc Electrophysiol; 2006 Nov; 17(11):1161-8. PubMed ID: 16911578
[TBL] [Abstract][Full Text] [Related]
16. Clinical characteristics and treatment of short QT syndrome.
Wolpert C; Schimpf R; Veltmann C; Giustetto C; Gaita F; Borggrefe M
Expert Rev Cardiovasc Ther; 2005 Jul; 3(4):611-7. PubMed ID: 16076272
[TBL] [Abstract][Full Text] [Related]
17. Successful management of cesarean section in a patient with Romano-Ward syndrome using landiolol, a selective and short-acting beta1 receptor antagonist.
Kubo K; Murao K; Nakao S; Kanoda T; Yamada M; Shingu K
J Anesth; 2005; 19(2):174-6. PubMed ID: 15875139
[TBL] [Abstract][Full Text] [Related]
18. [Romano Ward syndrome].
Stiskal A; Schlemmer M; Riedinger I; Wimmer M
Padiatr Padol; 1980; 15(1):67-75. PubMed ID: 7375119
[TBL] [Abstract][Full Text] [Related]
19. Clinical and molecular genetics of the short QT syndrome.
Schimpf R; Borggrefe M; Wolpert C
Curr Opin Cardiol; 2008 May; 23(3):192-8. PubMed ID: 18382206
[TBL] [Abstract][Full Text] [Related]
20. Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans.
Casimiro MC; Knollmann BC; Yamoah EN; Nie L; Vary JC; Sirenko SG; Greene AE; Grinberg A; Huang SP; Ebert SN; Pfeifer K
Genomics; 2004 Sep; 84(3):555-64. PubMed ID: 15498462
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]