Familial Amyloidotic Polyneuropathy in Sweden: Geographical Distribution, Age of Onset, and Prevalence von Sousa, Aida, Andersson, Rune, Drugge, Ulf, Holmgren, Gösta, Sandgren, Ola

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Familial amyloidotic polyneuropathy in Sweden: a pedigree analysis von Drugge, U, Andersson, R, Chizari, F, Danielsson, M, Holmgren, G, Sandgren, O, Sousa, A

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Alcohol-responsive myoclonic dystonia in a large family: Dominant inheritance and phenotypic variation von Kyllerman, M., Forsgren, L., Sanner, G., Holmgren, G., Wahlström, J., Drugge, U.

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Familial clustering of multiple sclerosis in a northern Swedish rural district von Binzer, M, Forsgren, L, Holmgren, G, Drugge, U, Fredrikson, S

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Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia von SCHUBACK, D, KRAMER, P, BRIN, M, DE LEON, D, BRESSMANS, MOSKOWITZ, C. B, BURKE, R. E, SANNER, G, DRUGGE, U, GUSELLA, J. F, FAHN, S, BREAKEFIELD, X. O, OZELIUS, L, HOLMGREN, G, FORSGREN, G, FORSGREN, L, KYLLERMAN, M, WAHLSTROMJ, CRAFT, C. M, NYGARD, T

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Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study von Drugge, U, Holmberg, M, Holmgren, G, Almay, B G, Linderholm, H

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Succinate dehydrogenase and aconitase deficiency in northern Sweden: A genealogical study von Drugge, U, Holmberg, M, Holmgren, G, Almay, BGL, Linderholm, H

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4-48-08 Familial amyloid neuropathy (FAP-type I) in Portugal and Sweden: A more variable disease than the one first described von Sousa, A., Barros, J., Coelho, T., Lobato, L., Drugge, U., Sandgren, O., Wikström, L., Andersson, R., Holmgren, G., Costa, P.P., Monteiro, L.S., Sequeiros, J.

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Study of individuals possibly affected with the fragile X syndrome in a large swedish family in the 18th to 20th centuries von Drugge, Ulf, Holmgren, GöSta, Blomquist, Hans Kison, Dahl, Niklas, Gustavson, Karl-Henrik, Malmgren, Helena

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Fragile X families in a Northern Swedish County: A genealogical study of possibly affected individuals in the nineteenth century von Drugge, Ulf, Blomquist, Hans K:son, Gustavson, Karl-Henrik, Holmgren, Gösta

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Fragile X families in a Northern Swedish county - a genealogical study demonstrating apparent paternal transmission from the 18th century von Holmgren, Gösta, Son Blomquist, Hans K., Drugge, Ulf, Gustavson, Karl-Henrik

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Geographical distribution of haplotypes in Swedish families with Huntington's disease von ALMQVIST, E, ANDREW, S, ANVRET, M, THEILMANN, J, GOLDBERG, P, ZEISLER, J, DRUGGE, U, GRANDELL, U, TAPPER-PERSSON, M, WINBLAD, B, HAYDEN, M

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The First Case of Familial Amyloidotic Polyneuropathy (FAP Met30) in the Finnish Population von Drugge, Ulf, Holmgren, Gösta, Udd, Bjarne

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Familial clustering of multiple sclerosis ina northern Swedish rural district von BINZER, M, FORSGREN, L, HOLMGREN, G, DRUGGE, U, FREDRIKSON, S

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POSITIVE END-EXPIRATORY PRESSURE VENTILATION AFTER OPEN-HEART SURGERY von DRUGGE, U., NORLANDER, O., OLSSON, P., RADEGRAN, K.

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Study of individuals possibly affected with the fragile X syndrome in a large Swedish family in the 18th to 20th centuries: X-linked mental retardation 5 von DRUGGE, U, HOLMGREN, G, DAHL, N, SON BLOMQUIST, H. K, GUSTAVSON, K.-H, MALMGREN, H

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Método para operação de um dispositivo sem fio von BERGSTRÖM MATTIAS, WIEMANN HENNING, YANG YU, DRUGGE OSKAR, KOORAPATY HAVISH, SAHLIN HENRIK, CHENG JUNG-FU

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Analysis of Globule Types in Malignant Melanoma von Xu, Jin, Gupta, Kapil, Stoecker, William V, Krishnamurthy, Yamini, Rabinovitz, Harold S, Bangert, Austin, Calcara, David, Oliviero, Margaret, Malters, Joseph M, Drugge, Rhett, Stanley, R. Joe, Moss, Randy H, Celebi, M. Emre

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A study on users' preference on interruption when using wearable computers and head mounted displays von Nilsson, Marcus, Drugge, Mikael, Liljedahl, Urban, Synnes, Kåre, Parnes, Peter

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UPLINK MAC PROTOCOL ASPECTS von YANG YU, HENRIK SAHLIN, HAVISH KOORAPATY, HENNING WIEMANN, MATTIAS BERGSTROEM, OSKAR DRUGGE, CHENG JUNG-FU

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