Search Results - "Lindstöm, M."

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    Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1 by Thornell, L.-E., Lindstöm, M., Renault, V., Klein, A., Mouly, V., Ansved, T., Butler-Browne, G., Furling, D.

    Published in Neuropathology and applied neurobiology (01-11-2009)
    “…Aims: Myotonic dystrophy type 1 (DM1), one of the most common forms of inherited neuromuscular disorders in the adult, is characterized by progressive muscle…”
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    Journal Article
  2. 2

    5-HTTLPR and COMTval158met genotype gate amygdala reactivity and habituation by Lonsdorf, Tina B., Golkar, Armita, Lindstöm, Kara M., Fransson, Peter, Schalling, Martin, Öhman, Arne, Ingvar, Martin

    Published in Biological psychology (01-04-2011)
    “…► Right amygdala reactivity 5-HTTLPR s-carrier > l/l. ► Left amygdala reactivity COMT met/met > val-carrier. ► 5-HTTLPR s-carrier show no amygdala habituation…”
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