Are vaccine shortages a relevant public health issue in Europe? A survey amongst countries participating in the EU-Joint Action on Vaccination, 2019 von Filia, A., Rota, M.C., Grossi, A., Martinelli, D., de Graaf, T., Dominguez, A., Tuells, J., Sormunen, P., Jønsrud, K., Johansen, K., Chene, G., Rezza, G.

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Outbreak of wound botulism in people who inject drugs, Norway, October to November 2013 von MacDonald, E, Arnesen, T M, Brantsaeter, A B, Gerlyng, P, Grepp, M, Hansen, B Å, Jønsrud, K, Lundgren, B, Mellegård, H, Møller-Stray, J, Rønning, K, Vestrheim, D F, Vold, L

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Are vaccine shortages a relevant public health issue in Europe? von Filia, A, Rota, M C, Grossi, A, Martinelli, D, De Graaf, T, Dominguez, A, Tuells, J, Sormunen, P, Jønsrud, K, Rezza, G

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Sequence comparison and mutational analysis of elements that may be involved in the regulation of DNA synthesis in HIV-1 von HUNGNES, O, JØNSRUD, K, TJØTTA, E, GRINDE, B

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Outbreak of wound botulism in people who inject drugs, Norway, October to November 2013 von MacDonald, E, Arnesen, T M, Brantsaeter, A B, Gerlyng, P, Grepp, M, Hansen, B Å, Jonsrud, K, Lundgren, B, Mellegård, H, Møller-Stray, J, Rønning, K, Vestrheim, D F, Vold, L

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A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy von Vissing, John, Barresi, Rita, Witting, Nanna, Van Ghelue, Marijke, Gammelgaard, Lise, Bindoff, Laurence A, Straub, Volker, Lochmüller, Hanns, Hudson, Judith, Wahl, Christoph M, Arnardottir, Snjolaug, Dahlbom, Kathe, Jonsrud, Christoffer, Duno, Morten

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MOTOR NEURON DISORDERS AND NEUROPATHIES von Müller, K., Nebuchenykh, M., Nilssen, Ø., Van Ghelue, M., Løseth, S., Jonsrud, C., Hoem, G., Arntzen, K.

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MOTOR NEURON DISORDERS AND NEUROPATHIES: EP.246 Kennedy disease in two sisters with biallelic CAG expansions of the androgen receptor gene von Müller, K., Nebuchenykh, M., Nilssen, Ø., Van Ghelue, M., Løseth, S., Jonsrud, C., Hoem, G., Arntzen, K.

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COLLAGEN RELATED MUSCLE DISEASES: EP.56 Collagen VI-related neuropathy von Arntzen, K., Müller, K., Løseth, S., Mellgren, S., Bågenholm, A., Halvorsen, H., Buvang, E., Hoem, G., Jonsrud, C., Van Ghelue, M.

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COLLAGEN RELATED MUSCLE DISEASES von Arntzen, K., Müller, K., Løseth, S., Mellgren, S., Bågenholm, A., Halvorsen, H., Buvang, E., Hoem, G., Jonsrud, C., Van Ghelue, M.

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FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation von De Baere, Elfride, Beysen, Diane, Oley, Christine, Lorenz, Birgit, Cocquet, Julie, De Sutter, Paul, Devriendt, Koen, Dixon, Michael, Fellous, Marc, Fryns, Jean-Pierre, Garza, Arturo, Jonsrud, Christoffer, Koivisto, Pasi A., Krause, Amanda, Leroy, Bart P., Meire, Françoise, Plomp, Astrid, Van Maldergem, Lionel, De Paepe, Anne, Veitia, Reiner, Messiaen, Ludwine

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EP.98Next-generation sequencing-based molecular diagnosis of neuromuscular patients: results of three years experience von Van Ghelue, M., Fagerheim, T., Hansen, G., Nygård, B., Arntzen, K., Ørstavik, K., Rasmussen, M., Nilssen, Ø., Jonsrud, C.

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MYOFIBRILLAR AND DISTAL MYOPATHIES von Orstavik, K., Almaas, V., Rasmussen, M., Jonsrud, C., Jensen, S., Loseth, S., Leren, T.

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MYOFIBRILLAR AND DISTAL MYOPATHIES: P.249A novel mutation in MYH7 giving rise to different phenotypes in a mother and her daughter von Orstavik, K., Almaas, V., Rasmussen, M., Jonsrud, C., Jensen, S., Loseth, S., Leren, T.

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CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA von Jonsrud, C., Aden, P., Hansen, G., Mork, M., Nygård, B., Popperud, T., Rasmussen, M., Songstad, N., Ørstavik, K., Fagerheim, T.

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CONGENITAL MYASTHENIC SYNDROMES AND MYASTHENIA: P.71Unexpected findings of congenital myasthenic syndromes by NGS testing using an extended gene panel on neuromuscular patients in... von Jonsrud, C., Aden, P., Hansen, G., Mork, M., Nygård, B., Popperud, T., Rasmussen, M., Songstad, N., Ørstavik, K., Fagerheim, T.

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CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy von Van Ghelue, M, Wahl, C, Arntzen, K, Loseth, S, Bindoff, L, Sveberg, L, Rosby, O, Popperud, T, Rasmussen, M, Halvorsen, H, Lindal, S, Jonsrud, C, Orstavik, K

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P.8.1 Muscle biopsy findings in Limb Girdle muscle Dystrophy 2I (LGMD2I) von Lindal, S, Myreng, K, Løseth, S, Jonsrud, C, Alhamidi, M, Stensland, E, Nilssen, Ø

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G.P.160 - CAPN3 mutation c. 643-663del21 identified in 52 Norwegian patients belonging to 24 families is associated with dominant calpainopathy von Van Ghelue, M., Wahl, C., Arntzen, K., Loseth, S., Bindoff, L., Sveberg, L., Rosby, O., Popperud, T., Rasmussen, M., Halvorsen, H., Lindal, S., Jonsrud, C., Orstavik, K.

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Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level von Weise, A, Gross, M, Mrasek, K, Mkrtchyan, H, Horsthemke, B, Jonsrud, C, Von Eggeling, F, Hinreiner, S, Witthuhn, V, Claussen, U, Liehr, T

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