Decision-making in job attendance within health care--a qualitative study von Tveten, K M, Morken, T

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Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13 von Jacob, Prince, Lindelöf, Hillevi, Rustad, Cecilie F., Sutton, Vernon Reid, Moosa, Shahida, Udupa, Prajna, Hammarsjö, Anna, Bhavani, Gandham SriLakshmi, Batkovskyte, Dominyka, Tveten, Kristian, Dalal, Ashwin, Horemuzova, Eva, Nordgren, Ann, Tham, Emma, Shah, Hitesh, Merckoll, Else, Orellana, Laura, Nishimura, Gen, Girisha, Katta M., Grigelioniene, Giedre

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Variants in the genes DCTN2, DNAH10, LRIG3, and MYO1A are associated with intermediate Charcot-Marie-Tooth disease in a Norwegian family von Braathen, G. J., Høyer, H., Busk, Ø. L., Tveten, K., Skjelbred, C. F., Russell, M. B.

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Interaction between the ligand-binding domain of the LDL receptor and the C-terminal domain of PCSK9 is required for PCSK9 to remain bound to the LDL receptor during endosomal acid... von TVETEN, Kristian, HOLLA, Øystein L, CAMERON, Jamie, BISMO STRØM, Thea, ERIK BERGE, Knut, LAERDAHL, Jon K, LEREN, Trond P

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Variants in the genes DCTN 2 , DNAH 10 , LRIG 3, and MYO 1A are associated with intermediate Charcot–Marie–Tooth disease in a Norwegian family von Braathen, G. J., Høyer, H., Busk, Ø. L., Tveten, K., Skjelbred, C. F., Russell, M. B.

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Fire Effects on Prairies and Oak Woodlands on Fort Lewis, Washington von Tveten, R K, Fonda, R W

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Identification of Bacteria Infecting Ixodes ricinus Ticks by 16S rDNA Amplification and Denaturing Gradient Gel Electrophoresis von Tveten, Ann-Kristin, Sjåstad, Knut K.

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Salmon lice sampled from wild Atlantic salmon and sea trout throughout Norway display high frequencies of the genotype associated with pyrethroid resistance von Fjørtoft, Helene Børretzen, Nilsen, Frank, Besnier, Francois, Stene, Anne, Bjørn, Pål Arne, Tveten, Ann-Kristin, Aspehaug, Vidar Teis, Finstad, Bengt, Glover, Kevin Alan

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Functional analysis of the synonymous R385R mutation in the low-density lipoprotein receptor gene von Tveten, Kristian, Khoo, Kah-Lin, Berge, Knut Erik, Leren, Trond P, Kulseth, Mari Ann

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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature von Rots, D., Chater-Diehl, E., Dingemans, A.J.M., Goodman, S.J., Siu, M.T., Cytrynbaum, C., Choufani, S., Hoang, N., Walker, S., Awamleh, Z., Charkow, J., Meyn, S., Pfundt, R., Rinne, T., Gardeitchik, T., Vries, B.B.A. de, Deden, A.C., Leenders, E., Kwint, M., Stumpel, C.T.R.M., Stevens, S.J.C., Vermeulen, J.R., Harssel, J.V.T. van, Bosch, D.G.M., Gassen, K.L.I. van, Binsbergen, E. van, Geus, C.M. de, Brackel, H., Hempel, M., Lessel, D., Denecke, J., Slavotinek, A., Strober, J., Crunk, A., Folk, L., Wentzensen, I.M., Yang, H., Zou, F.G., Millan, F., Person, R., Xie, Y.L., Liu, S.X., Ousager, L.B., Larsen, M., Schultz-Rogers, L., Morava, E., Klee, E.W., Berry, I.R., Campbell, J., Lindstrom, K., Pruniski, B., Neumeyer, A.M., Radley, J.A., Phornphutkul, C., Schmidt, B., Wilson, W.G., Ounap, K., Reinson, K., Pajusalu, S., Haeringen, A. van, Ruivenkamp, C., Cuperus, R., Santos-Simarro, F., Palomares-Bralo, M., Pacio-Miguez, M., Ritter, A., Bhoj, E., Tonne, E., Tveten, K., Cappuccio, G., Brunetti-Pierri, N., Rowe, L., Bunn, J., Saenz, M., Platzer, K., Mertens, M., Caluseriu, O., Nowaczyk, M.J.M., Cohn, R.D., Kannu, P., Alkhunaizi, E., Chitayat, D., Scherer, S.W., Brunner, H.G., Vissers, L.E.L.M., Kleefstra, T., Koolen, D.A., Weksberg, R.

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PAPSS2‐related brachyolmia : clinical and radiological phenotype in 18 new cases von Bownass, L, Abbs, S, Armstrong, R, Baujat, G, Behzadi, G, Berentsen, R.D, Burren, C, Calder, A, Cormier‐Daire, V, Newbury‐Ecob, R, Foulds, N, Juliusson, P.B, Kant, S.G, Lefroy, H, Mehta, S.G, Merckoll, E, Michot, C, Monsell, F, Offiah, A.C, Richards, A, Rosendahl, K, Rustad, C.F, Shears, D, Tveten, K, Wellesley, D, Wordsworth, P, Smithson, S

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Supplementary Material for: Genetic epidemiology of amyotrophic lateral sclerosis in Norway – a 2-year population based study von C.G., Olsen, Ø.L., Busk, T.N., Aanjesen, K.B., Alstadhaug, I.K., Bjørnå, G.J., Braathen, K.L., Breivik, N., Demic, H.Ø., Flemmen, E., Hallerstig, I., HogenEsch, Ø.L., Holla, A.B., Jøntvedt, M.T., Kampman, G., Kleveland, H.B., Kvernmo, U., Ljøstad, A., Maniaol, Å.H., Morsund, O., Nakken, C., Novy, T., Rekand, K., Schlüter, S., Schuler, K., Tveten, O.-B., Tysnes, T., Holmøy, H., Høyer

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Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry von Crotti, L, Spazzolini, C, Tester, DJ, Ghidoni, A, Baruteau, A-E, Beckmann, B-M, Behr, ER, Bennett, JS, Bezzina, CR, Bhuiyan, ZA, Celiker, A, Cerrone, M, Dagradi, F, De Ferrari, GM, Etheridge, SP, Fatah, M, Garcia-Pavia, P, Al-Ghamdi, S, Hamilton, RM, Al-Hassnan, ZN, Horie, M, Jimenez-Jaimez, J, Kanter, RJ, Kaski, JP, Kotta, M-C, Lahrouchi, N, Makita, N, Norrish, G, Odland, HH, Ohno, S, Papagiannis, J, Parati, G, Sekarski, N, Tveten, K, Vatta, M, Webster, G, Wilde, AAM, Wojciak, J, George, AL, Ackerman, MJ, Schwartz, PJ

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability von Kury, S., Woerden, G.M. van, Besnard, T., Onori, M.P., Latypova, X., Towne, M.C., Cho, M.T., Prescott, T.E., Ploeg, M.A., Sanders, S., Stessman, H.A.F., Pujol, A., Distel, ben, Robak, L.A., Bernstein, J.A., Denomme-Pichon, A.S., Lesca, G., Sellars, E.A., Berg, J., Carre, W., Busk, O.L., Bon, B.W.M. van, Waugh, J.L., Deardorff, M., Hoganson, G.E., Bosanko, K.B., Johnson, D.S., Dabir, T., Holla, O.L., Sarkar, A., Tveten, K., Bellescize, J. de, Braathen, G.J., Terhal, P.A., Grange, D.K., Haeringen, A. van, Lam, C., Mirzaa, G., Burton, J., Bhoj, E.J., Douglas, J., Santani, A.B., Nesbitt, A.I., Helbig, K.L., Andrews, M.V., Begtrup, A., Tang, S., Gassen, K.L.I. van, Juusola, J., Foss, K., Enns, G.M., Moog, U., Hinderhofer, K., Paramasivam, N., Lincoln, S., Kusako, B.H., Lindenbaum, P., Charpentier, E., Nowak, C.B., Cherot, E., Simonet, T., Ruivenkamp, C.A.L., Hahn, S., Brownstein, C.A., Xia, F., Schmitt, S., Deb, W., Bonneau, D., Nizon, M., Quinquis, D., Chelly, J., Rudolf, G., Sanlaville, D., Parent, P., Gilbert-Dussardier, B., Toutain, A., Peart-Vissers, L.E.L.M., Boisseau, P., Vincent, M., Grabrucker, A.M., Dubourg, C., Tan, W.H., Verbeek, N.E., Granzow, M., Santen, G.W.E., Shendure, J., Isidor, B., Pasquier, L., Redon, R., Yang, Y.P., State, M.W., Kleefstra, T., Cogne, B., Petrovski, S., Retterer, K., Eichler, E.E., Agrawal, P.B., Bezieau, S., Odent, S., Elgersma, Y.

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NO752284L von TVETEN K, KRISTIANSEN P

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Strong enhancement of level densities in the crossover from spherical to deformed neodymium isotopes von Guttormsen, M., Alhassid, Y., Ryssens, W., Ay, K.O., Ozgur, M., Algin, E., Larsen, A.C., Bello Garrote, F.L., Crespo Campo, L., Dahl-Jacobsen, T., Görgen, A., Hagen, T.W., Ingeberg, V.W., Kheswa, B.V., Klintefjord, M., Midtbø, J.E., Modamio, V., Renstrøm, T., Sahin, E., Siem, S., Tveten, G.M., Zeiser, F.

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Radiative Width of the Hoyle State from γ -Ray Spectroscopy von Kibédi, T., Alshahrani, B., Stuchbery, A. E., Larsen, A. C., Görgen, A., Siem, S., Guttormsen, M., Giacoppo, F., Morales, A. I., Sahin, E., Tveten, G. M., Garrote, F. L. Bello, Campo, L. Crespo, Eriksen, T. K., Klintefjord, M., Maharramova, S., Nyhus, H.-T., Tornyi, T. G., Renstrøm, T., Paulsen, W.

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PREPARATION OF MAGNESIUM CHLORIDE von ANDREASSEN K, LUNDE R, TVETEN K, BOEYUM O, BLAKER I

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NO122915B von SOLBERG P, ERIKSEN K, TVETEN K, BOEYUM O

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NO122916B von ANDREASSEN K, LUNDE R, TVETEN K, BOEYUM O, BLAKER I

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