Authors:
Tyson, J
Tranebjaerg, L
McEntagart, M
Larsen, LA
Christiansen, M
Whiteford, ML
Bathen, J
Aslaksen, B
Sorland, SJ
Lund, O
Pembrey, ME
Malcolm, S
Bitner-Glindzicz, M
Citation: J. Tyson et al., Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen (vol 107, pg 499, 2000), HUM GENET, 108(1), 2001, pp. 75-75
Authors:
Larsen, LA
Andersen, PS
Kanters, J
Svendsen, IH
Jacobsen, JR
Vuust, J
Wettrell, G
Tranebjaerg, L
Bathen, J
Christiansen, M
Citation: La. Larsen et al., Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome, CLIN CHEM, 47(8), 2001, pp. 1390-1395
Authors:
Tyson, J
Tranebjaerg, L
McEntagart, M
Larsen, LA
Christiansen, M
Whiteford, ML
Bathen, J
Aslaksen, B
Sorland, SJ
Lund, O
Pembrey, ME
Malcolm, S
Bitner-Glindzicz, M
Citation: J. Tyson et al., Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen, HUM GENET, 107(5), 2000, pp. 499-503
Authors:
Sjaastad, O
Lindboe, CF
Schaanning, J
Brodtkorb, E
Kearney, M
Hovig, T
Salvesen, R
Haugnes, T
Rokseth, R
Smethurst, HB
Sand, T
Dale, LG
Bathen, J
Citation: O. Sjaastad et al., Familial mydriasis, cardiac arrhythmia, respiratory failure, muscular weakness and hypohidrosis, ACT NEUR SC, 102, 2000, pp. 3-31
Authors:
Pleym, H
Bathen, J
Spigset, O
Gisvold, SE
Citation: H. Pleym et al., Ventricular fibrillation related to reversal of the neuromuscular blockadein a patient with long QT syndrome, ACT ANAE SC, 43(3), 1999, pp. 352-355