CareLit · DOI-Nachweis · Klinische Neurophysiologie
Cerebral white matter affection in myotonic dystrophy type 1 and 2– A Diffusion-Tensor-Imaging Study at3T
DOI 10.1055/s-0030-1250929
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Nachweis in CareLit
Autor:innenM Minnerop, JC Schöne-Bake, S Mirbach, S Röske, C Schneider-Gold, RC Betz, C Helmstaedter, M Tittgemeyer, T Klockgether, C Kornblum
ZeitschriftKlinische Neurophysiologie
Ausgabe03/2010
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Myotonic dystrophy type 1 (DM1) and 2 (DM2) are autosomal dominantly inherited neuromuscular disorders with multisystemic involvement. Although cognitive impairment and white matter changes are more common in DM1 patients, brain volume loss and white matter changes have been described in DM2 patients as well. Using voxel-based morphometry (VBM) we previously found grey and white matter loss along cerebral midline st…
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Zitierempfehlung
M Minnerop, JC Schöne-Bake, S Mirbach, S Röske, C Schneider-Gold, RC Betz, C Helmstaedter, M Tittgemeyer, T Klockgether, C Kornblum (2010) Cerebral white matter affection in myotonic dystrophy type 1 and 2– A Diffusion-Tensor-Imaging Study at3T. Klinische Neurophysiologie (03). https://doi.org/10.1055/s-0030-1250929
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