Search Results - "Weinsheimer, S M"

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  1. 1

    Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasia by Thompson, K P, Nelson, J, Kim, H, Weinsheimer, S M, Marchuk, D A, Lawton, M T, Krings, T, Faughnan, M E

    Published in Orphanet journal of rare diseases (19-09-2021)
    “…Approximately 10% of hereditary hemorrhagic telangiectasia (HHT) patients harbour brain vascular malformations (VMs). Intracranial hemorrhage (ICH) from brain…”
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    Journal Article
  2. 2

    Clinical segmentation in 22q11.2 deletion syndrome: Cognitive impairments and additional genetic load by Schmock, H., Stevenson, Matt P., Hanebaum, S., Vangkilde, A., Rosengren, A., Weinsheimer, S.M., Skovby, F., Olesen, C., Ullum, H., Baaré, W.F.C., Siebner, H.R., Didriksen, M., Werge, T., Olsen, L., Jepsen, J.R.M.

    Published in Journal of psychiatric research (01-09-2024)
    “…The 22q11.2 deletion syndrome (22q11.2DS) is associated with high psychiatric morbidity. However, large phenotypic heterogeneity hampers early detection of…”
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    Journal Article