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Results: 1-13 |
Results: 13

Authors: Haug, K Kohlschmidt, N Dereser-Dennl, M Zielinski, J Merz, E Schafer, D
Citation: K. Haug et al., Familial fatal fetal cardiomyopathy with isolated myocardial calcifications: A new syndrome?, AM J MED G, 101(3), 2001, pp. 255-258

Authors: Escayg, A Heils, A MacDonald, BT Haug, K Sander, T Meisler, MH
Citation: A. Escayg et al., A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus - and prevalence of variants in patients with epilepsy, AM J HU GEN, 68(4), 2001, pp. 866-873

Authors: Haug, K Jenkins, T
Citation: K. Haug et T. Jenkins, Effects of hydrogen on the three-dimensional epitaxial growth of Ni(100), (110), and (111), J PHYS CH B, 104(43), 2000, pp. 10017-10023

Authors: Haug, K Sander, T Hallmann, K Rau, B Dullinger, JS Elger, CE Propping, P Heils, A
Citation: K. Haug et al., The voltage-gated sodium channel beta 2-subunit gene and idiopathic generalized epilepsy, NEUROREPORT, 11(12), 2000, pp. 2687-2689

Authors: Haug, K Hallmann, K Horvath, S Sander, T Kubisch, C Rau, B Dullinger, J Beyenburg, S Elger, CE Propping, P Heils, A
Citation: K. Haug et al., No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy, EPILEPSY R, 42(1), 2000, pp. 57-62

Authors: Haug, K Sander, T Hallmann, K Lentze, MJ Propping, P Elger, CE Heils, A
Citation: K. Haug et al., Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy, EPILEPSY R, 39(2), 2000, pp. 127-132

Authors: Haug, K Kremerskothen, J Hallmann, K Sander, T Dullinger, J Rau, B Beyenburg, S Lentze, MJ Barnekow, A Elger, CE Propping, P Heils, A
Citation: K. Haug et al., Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy, MOL CELL PR, 14(4), 2000, pp. 255-260

Authors: Heils, A Haug, K Kunz, WS Fernandez, G Horvath, S Rebstock, J Propping, P Elger, CE
Citation: A. Heils et al., Interleukin-1 beta gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosis, ANN NEUROL, 48(6), 2000, pp. 948-949

Authors: Haug, K Khan, S Fuchs, S Konig, R
Citation: K. Haug et al., OFD II, OFD VI, and Joubert syndrome manifestations in 2 sibs, AM J MED G, 91(2), 2000, pp. 135-137

Authors: Gohlke, BC Haug, K Fukami, M Friedl, W Noeker, M Rappold, GA Haverkamp, F
Citation: Bc. Gohlke et al., Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy, J MED GENET, 37(8), 2000, pp. 600-602

Authors: Haug, K Irgens, LM Skjaerven, R Markestad, T Baste, V Schreuder, P
Citation: K. Haug et al., Maternal smoking and birthweight: effect modification of period, maternal age and paternal smoking, ACT OBST SC, 79(6), 2000, pp. 485-489

Authors: Holme, JA Haddeland, U Haug, K Brunborg, G
Citation: Ja. Holme et al., DNA damage induced by the drinking water mutagen 3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone (MX) in mammalian cells in vitro and in mice, MUT RES-GTE, 441(1), 1999, pp. 145-153

Authors: Haug, K Do, NKN
Citation: K. Haug et Nkn. Do, Kinetic Monte Carlo study of the effect of hydrogen on the two-dimensionalepitaxial growth of Ni(100), PHYS REV B, 60(15), 1999, pp. 11095-11101
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