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Results: 1-6 |
Results: 6

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: Ostman-Smith, I Wettrell, G
Citation: I. Ostman-smith et G. Wettrell, Pathophysiology of hypertrophic cardiomyopathy, LANCET, 355(9207), 2000, pp. 928-928

Authors: Larsen, LA Fosdal, I Andersen, PS Kanters, JK Vuust, J Wettrell, G Christiansen, M
Citation: La. Larsen et al., Recessive Romano-Ward syndrome associated with compound heterozygosity fortwo mutations in the KVLQT1 gene, EUR J HUM G, 7(6), 1999, pp. 724-728

Authors: Ostman-Smith, I Wettrell, G Riesenfeld, T
Citation: I. Ostman-smith et al., A cohort study of childhood hypertrophic cardiomyopathy - Improved survival following high-dose beta-adrenoceptor antagonist treatment, J AM COL C, 34(6), 1999, pp. 1813-1822

Authors: Ahlstrom, H Alvero, J Alvero, R Espos, R Fajutrao, L Herrera, J Kjellman, B Kubista, J Leviste, C Meyer, P Oldaeus, G Siricururat, A Vichyanond, P Wettrell, G Wong, E Laxmyr, L Nyberg, L Olsson, H Weibull, E Rosenborg, J
Citation: H. Ahlstrom et al., Pharmacokinetics of bambuterol during oral administration to asthmatic children, BR J CL PH, 48(3), 1999, pp. 299-308

Authors: Ekstrom, U Abrahamson, M Floren, CH Tollig, H Wettrell, G Nilsson, E Sun, XM Soutar, AK Nilsson-Ehle, P
Citation: U. Ekstrom et al., An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F), CLIN GENET, 55(5), 1999, pp. 332-339
Risultati: 1-6 |