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105 Room for Intravascular Volume Expansion in Emergency Department Stroke Management von Miller, J, Rodriguez, L, Levely, J, Lee, A, Devisser, M, Gao, Y, Suszanski, J, Lewandowski, C

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Towards evolutionary predictions: Current promises and challenges von Wortel, Meike T., Agashe, Deepa, Bailey, Susan F., Bank, Claudia, Bisschop, Karen, Blankers, Thomas, Cairns, Johannes, Colizzi, Enrico Sandro, Cusseddu, Davide, Desai, Michael M., Dijk, Bram, Egas, Martijn, Ellers, Jacintha, Groot, Astrid T., Heckel, David G., Johnson, Marcelle L., Kraaijeveld, Ken, Krug, Joachim, Laan, Liedewij, Lässig, Michael, Lind, Peter A., Meijer, Jeroen, Noble, Luke M., Okasha, Samir, Rainey, Paul B., Rozen, Daniel E., Shitut, Shraddha, Tans, Sander J., Tenaillon, Olivier, Teotónio, Henrique, Visser, J. Arjan G. M., Visser, Marcel E., Vroomans, Renske M. A., Werner, Gijsbert D. A., Wertheim, Bregje, Pennings, Pleuni S.

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FROM THE SPINAL CORD TO THE MUSCLE von Alonso-Pérez, J., Gonález-Quereda, L., Semplicini, C., Gallano, P., Pegoraro, E., Nascimento, A., Ortez, C., Devisser, M., Van der Krooi, A., Garrido, C., Santos, M., Guglieri, M., Straub, V., Schara, U., Study group, S. Sarcoglycan, Díaz-Manera, J.

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FROM THE SPINAL CORD TO THE MUSCLE: O.10 European collaboration on the clinical and genetic spectrum of sarcoglycan-deficient muscular dystrophy von Alonso-Pérez, J., Gonález-Quereda, L., Semplicini, C., Gallano, P., Pegoraro, E., Nascimento, A., Ortez, C., Devisser, M., Van der Krooi, A., Garrido, C., Santos, M., Guglieri, M., Straub, V., Schara, U., Study group, S. Sarcoglycan, Díaz-Manera, J.

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Sex slows down the accumulation of deleterious mutations in the homothallic fungus Aspergillus nidulans von Bruggeman, Judith, Debets, Alfons J M, Wijngaarden, Pieter J, deVisser, J Arjan G M, Hoekstra, Rolf F

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Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures von Jöbsis, G. Joost, Keizers, H, Vreijling, Jeroen P, Visser, Marianne de, Speer, Marcy C, Wolterman, Ruud A, Baas, Frank, Bolhuis, Pieter A

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Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy von COBBEN, J. M, VAN DER STEEGE, G, GROOTSCHOLTEN, P, DE VISSER, M, SCHEFFER, H, BUYS, C. H. C. M

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Nemaline myopathy : current concepts von NORTH, K. N, LAING, N. G, WALLGREN-PETTERSSON, C

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Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21 von VAN DER KOOI, A. J, VAN MEEGEN, M, LEDDERHOF, T. M, MCNALLY, E. M, DE VISSER, M, BOLHUIS, P. A

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Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A von Valentijn, Linda J, Baas, Frank, Wolterman, Ruud A, Hoogendijk, Jessica E, van den Bosch, Norbert H.A, Zorn, Ina, Gabreëls-Festen, Anneke A.W.M, de Visser, Marianne, Bolhuis, Pieter A

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A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement von van der Kooi, A. J., Ledderhof, T. M., DeVoogt, W. G., Res, J. C. J., Bouwsma, G., Troost, D., Busch, H. F. M., Becker, A. E., DeVisser, M.

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DENOVO MUTATION IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-1 von HOOGENDIJK, JE, HENSELS, GW, GABREELSFESTEN, AAWM, GABREELS, FJM, JANSSEN, EAM, DEJONGHE, P, MARTIN, JJ, VAN BROECKHOVEN, C, VALENTIJN, LJ, BAAS, F, DEVISSER, M, BOLHUIS, PA

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Miyoshi-type distal muscular dystrophy : Clinical spectrum in 24 Dutch patients von LINSSEN, W. H. J. P, NOTERMANS, N. C, VAN DER GRAAF, Y, WOKKE, J. H. J, VAN DOORN, P. A, HÖWELER, C. J, BUSCH, H. F. M, DE JAGER, A. E. J, DE VISSER, M

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Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period von HOOGERWAARD, E. M, DE VOOGT, W. G, WILDE, A. A. M, VAN DER WOUW, P. A, BAKKER, E, VAN OMMEN, G.-J. B, DE VISSER, M

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The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands von van der Kooi, A. J., Barth, P. G., Busch, H. F. M., de Haan, R., Ginjaar, H. B., van Essen, A. J., van Hooff, L. J. M. A., Höweler, C. J., Jennekens, F. G. I., Jongen, P., Oosterhuis, H. J. G. H., Padberg, G. W. A. M., Spaans, F., Wintzen, A. R., Wokke, J. H. J., Bakker, E., van Ommen, G. J. B., Bolhuis, P. A., de Visser, M.

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Hereditary motor and sensory neuropathy type I: Clinical and neurographical features of the 17p duplication subtype von Hoogendijk, Jessica E., de Visser, Marianne, Bolhuis, Pieter A., Hart, Augustinus A. M., de Visser, Bram W. Ongerboer

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Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1) von KEMP, E. A. M. J. S, HENSELS, G. W, SIE, O. G, DE DIE-SMULDERS, C. E. M, HOOGENDIJK, J. E, DE VISSER, M, BOLHUIS, P. A

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Estimates of the Rate and Distribution of Fitness Effects of Spontaneous Mutation in Saccharomyces cerevisiae von Zeyl, C, Arjan, J, DeVisser, G M

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Genetic localization of Bethlem myopathy von JÖBSIS, G. J, BOLHUIS, P. A, BOERS, J. M, BAAS, F, WOLTERMAN, R. A, HENSELS, G. W, DE VISSER, M

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