Search Results - "van den Boom, Rivka"

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  1. 1

    Descriptive Analysis of the Boston Criteria Applied to a Dutch-Type Cerebral Amyloid Angiopathy Population by VAN ROODEN, Sanneke, VAN DER GROND, Jeroen, VAN DEN BOOM, Rivka, HAAN, Joost, LINN, Jennifer, GREENBERG, Steven M, VAN BUCHEM, Mark A

    Published in Stroke (1970) (01-09-2009)
    “…Validation of the Boston criteria for the in vivo diagnosis of cerebral amyloid angiopathy (CAA) is challenging, because noninvasive diagnostic tests do not…”
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  2. 2

    Lacunar infarcts are the main correlate with cognitive dysfunction in cadasil by LIEM, Michael K, VAN DER GROND, Jeroen, HAAN, Joost, BOOM, Rivka Van Den, FERRARI, Michel D, KNAAP, Yvette M, BREUNING, Martijn H, VAN BUCHEM, Mark A, MIDDELKOOP, Huub A. M, OBERSTEIN, Saskia A. J. Lesnik

    Published in Stroke (1970) (01-03-2007)
    “…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy is caused by mutations in the NOTCH3 gene and is clinically…”
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  3. 3

    Cerebral Hemodynamics and White Matter Hyperintensities in CADASIL by van den Boom, Rivka, Oberstein, Saskia A. Lesnik, Spilt, Aart, Behloul, Faiza, Ferrari, Michel D., Haan, Joost, Westendorp, Rudi G., van Buchem, Mark A.

    “…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary small-vessel disease caused by mutations…”
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  4. 4
  5. 5

    Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: MR imaging findings at different ages--3rd-6th decades by van den Boom, Rivka, Lesnik Oberstein, Saskia A J, Ferrari, Michel D, Haan, Joost, van Buchem, Mark A

    Published in Radiology (01-12-2003)
    “…To depict various brain lesions that have been described in patients who have cerebral autosomal dominant arteriopathy with subcortical infarcts and…”
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  8. 8

    Subcortical lacunar lesions: an MR imaging finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy by van Den Boom, Rivka, Lesnik Oberstein, Saskia A J, van Duinen, Sjoerd G, Bornebroek, Marjolijn, Ferrari, Michel D, Haan, Joost, van Buchem, Mark A

    Published in Radiology (01-09-2002)
    “…To assess the prevalence and distribution of subcortical lacunar lesions (SLLs) in patients with cerebral autosomal dominant arteriopathy with subcortical…”
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  9. 9

    Evaluation of diagnostic NOTCH3 immunostaining in CADASIL by OBERSTEIN, Saskia A. J. Lesnik, VAN DUINEN, Sjoerd G, VAN DEN BOOM, Rivka, MAAT-SCHIEMAN, Marion L. C, VAN BUCHEM, Mark A, VAN HOUWELINGEN, Hans C, HEGEMAN-KLEINN, Ingrid M, FERRARI, Michel D, BREUNING, Martijn H, HAAN, Joost

    Published in Acta neuropathologica (01-08-2003)
    “…CADASIL is caused by mutations in the NOTCH3 gene. Although increasingly recognized as a disease entity, the diagnostic confirmation can be lengthy or…”
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  10. 10

    No Influence of Melatonin on Cerebral Blood Flow in Humans by van der Helm-van Mil, Annette H. M., van Someren, Eus J. W., van den Boom, Rivka, van Buchem, Mark A., de Craen, Anton J. M., Blauw, Gerard J.

    “…Melatonin has been attributed a role in a number of physiological processes. Changes in distal skin temperature and blood pressure after intake of melatonin…”
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  11. 11

    MR assessment of cerebral vascular response: A comparison of two methods by Spilt, Aart, Van den Boom, Rivka, Kamper, Adriaan M., Blauw, Gerard J., Bollen, Edward L.E.M., van Buchem, Mark A.

    Published in Journal of magnetic resonance imaging (01-11-2002)
    “…Purpose To compare the results and reproducibility of two MR‐based methods of measuring the cerebrovascular response (CVR). Materials and Methods In eight…”
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  12. 12

    Incipient CADASIL by Lesnik Oberstein, Saskia A J, van den Boom, Rivka, Middelkoop, Huub A M, Ferrari, Michel D, Knaap, Yvette M, van Houwelingen, Hans C, Breuning, Martijn H, van Buchem, Mark A, Haan, Joost

    Published in Archives of neurology (Chicago) (01-05-2003)
    “…Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the NOTCH3 gene. Knowledge of…”
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