Linkage of ischemic stroke to the PDE4D region on 5q in a Swedish population von NILSSON-ARDNOR, Sofie, WIKLUND, Per-Gunnar, LINDGREN, Petter, NILSSON, Anna Karin, JANUNGER, Tomas, ESCHER, Stefan A, HALLBECK, Björn, STEGMAYR, Birgitta, ASPLUND, Kjell, HOLMBERG, Dan

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A novel stroke locus identified in a northern Sweden pedigree: Linkage to chromosome 9q31-33 von JANUNGER, T, NILSSON-ARDNOR, S, WIKLUND, P.-G, LINDGREN, P, ESCHER, S. A, LACKOVIC, K, NILSSON, A. K, STEGMAYR, B, ASPLUND, K, HOLMBERG, D

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Genome-wide linkage scan of common stroke in families from northern Sweden von NILSSON-ARDNOR, Sofie, JANUNGER, Tomas, WIKLUND, Per-Gunnar, LACKOVIC, Kurt, KARIN NILSSON, Anna, LINDGREN, Petter, ESCHER, Stefan A, STEGMAYR, Birgitta, ASPLUND, Kjell, HOLMBERG, Dan

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The genetic contribution to stroke in northern Sweden von Janunger, Tomas

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Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser von Janunger, Tomas, Anan, Intissar, Holmgren, Gösta, Lövheim, Olov, Ohlsson, Per-Ingvar, Suhr, Ole B., Tashima, Kazuhiro

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Ocular Phenotype of Bothnia Dystrophy, an Autosomal Recessive Retinitis Pigmentosa Associated With an R234W Mutation in the RLBP1 Gene von Burstedt, Marie S. I, Forsman-Semb, Kristina, Golovleva, Irina, Janunger, Tomas, Wachtmeister, Lillemor, Sandgren, Ola

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