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Journal of the Neurological Sciences|May 1, 1990
Cytochrome P450 and Parkinson's disease. Poor parahydroxylation of phenytoinM D Ferrari, E A Peeters, J Haan, et al.Stroke|August 26, 1998
Microvasculopathy is associated with the number of cerebrovascular lesions in hereditary cerebral hemorrhage with amyloidosis, Dutch typeR Natté, H V Vinters, M L Maat-Schieman, et al.Alzheimer Disease and Associated Disorders|January 1, 1996
Hereditary cerebral hemorrhage with amyloidosis-Dutch type: better correlation of cognitive deterioration with advancing age than with number of focal lesions or white matter hyperintensitiesM Bornebroek, M A Van Buchem, J Haan, et al.Nuclear Medicine Communications|November 1, 1996
Potential for imaging cerebral amyloid deposits using 123I-labelled serum amyloid P component and SPETM Bornebroek, J F Verzijlbergen, J Haan, et al.Neuroradiology|January 1, 1990
Hereditary cerebral hemorrhage with amyloidosis--Dutch type. Tc-99m HM-PAO single photon emission computed tomographyJ Haan, M J van Kroonenburgh, P R Algra, et al.Archives of Neurology|January 1, 1996
White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutationM Bornebroek, J Haan, M A van Buchem, et al.Science (New York, N.Y.)|June 1, 1990
Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)C Van Broeckhoven, J Haan, E Bakker, et al.Annals of Neurology|May 1, 1997
Dutch hereditary cerebral amyloid angiopathy: structural lesions and apolipoprotein E genotypeM Bornebroek, J Haan, S G Van Duinen, et al.Annals of Neurology|July 1, 1997
Presenilin-1 polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch typeM Bornebroek, J Haan, H Backhovens, et al.Pageof 33