N Colman, K Nahm, KS Ganzeboom, WK Shen, … - Clinical Autonomic Research, 2004 - Springer N. Colman · KS Ganzeboom · W.Wieling ( ) Dept. of Internal Medicine, Room
F4-221 Academic Medical Centre PO Box 22700 1100 DE Amsterdam, The Netherlands
Tel.: +31-20/5665990 Fax: +31-20/6914904 E-Mail: w.wieling@amc.uva.nl N. ... Cited by 52 - Related articles - BL Direct - All 3 versions
- ►nih.gov G Berecki, JG Zegers, ZA Bhuiyan, AO … - The Journal of Physiology, 2006 - Physiological Soc Long-QT3 syndrome (LQT3) is linked to cardiac sodium channel gene (SCN5A)
mutations. In this study, we used the 'dynamic action potential clamp' (dAPC)
technique to effectively replace the native sodium current (I Na ) of the ... Cited by 16 - Related articles - BL Direct - All 13 versions
SK Chung, JM MacCormick, CH McCulley, J … - Heart Rhythm, 2007 - Elsevier Genetic testing in long QT syndrome (LQTS) is moving from research into clinical
practice. We have recently piloted a molecular genetics program in a New Zealand
research laboratory with a view to establishing a clinical diagnostic service. Cited by 12 - Related articles - All 2 versions
- ►cinc.org [PDF] JJ Struijk, JK Kanters, MP Andersen, T Hardahl … - Medical and Biological Engineering and Computing, 2006 - Springer Abstract The long QT syndrome (LQTS) is a genetic disorder, typically
characterized by a prolonged QT interval in the ECG due to abnormal cardiac
repolar- ization. LQTS may lead to syncopal episodes and sudden cardiac ... Cited by 12 - Related articles - BL Direct - All 9 versions
PJ Mohler, XHT Wehrens - Physiology, 2007 - Am Physiological Soc Most ion channels are multi-subunit complexes, involving an arrangement of
proteins closely packed around a water-filled pore that extends through the
plane of the membrane (50). The principal, pore-forming subunits are known ... Cited by 7 - Related articles - BL Direct - All 6 versions
ND Patel, BK Singh, ST Mathew - European Journal of Internal Medicine, 2006 - Elsevier The long QT syndrome affects predominantly younger people who demonstrate
structurally normal hearts. The underlying defect in the long QT syndrome seems
to be genetic mutations in the cardiac ionic channels responsible for ... Cited by 7 - Related articles - All 10 versions
S Behl, TD Wauchob - International Journal of Obstetric Anesthesia, 2005 - Elsevier We describe the anaesthetic management of a spontaneous vaginal delivery at 39
weeks' gestation in a 22-year-old patient with congenital long QT syndrome. With
a strong family history of sudden deaths, the patient had an initial QT ... Cited by 3 - Related articles - All 3 versions
- ►physiology.org T Chen, M Inoue, MF Sheets - American Journal of Physiology- Heart and Circulatory …, 2005 - Am Physiological Soc Deletion of a phenylalanine at position 1617 (delF1617) in the extracellular
linker between segments S3 and S4 in domain IV of the human heart Na + channel
(hH1a) has been tentatively associated with long QT syndrome type 3 (LQT3). ... Cited by 3 - Related articles - All 4 versions
