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P Cras

Showing results (101-110 of 119) with videos related to

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Nature Genetics|June 1, 1992
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein geneL Hendriks, C M van Duijn, P Cras, et al.
Neurology|October 8, 2008
Progranulin variability has no major role in Parkinson disease genetic etiologyK Nuytemans, P Pals, K Sleegers, et al.
Acta Neuropathologica|October 1, 1998
Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala-->Gly mutationP Cras, F van Harskamp, L Hendriks, et al.
Annals of Neurology|November 15, 2001
Endocytic disturbances distinguish among subtypes of Alzheimer's disease and related disordersA Cataldo, G W Rebeck, B Ghetri, et al.
Brain : a Journal of Neurology|November 10, 2001
Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutationB Dermaut, S Kumar-Singh, C De Jonghe, et al.
Neurobiology of Disease|February 15, 2000
Behavioral disturbances without amyloid deposits in mice overexpressing human amyloid precursor protein with Flemish (A692G) or Dutch (E693Q) mutationS Kumar-Singh, I Dewachter, D Moechars, et al.
Neurology|May 20, 1999
Improved discrimination of AD patients using beta-amyloid(1-42) and tau levels in CSFF Hulstaert, K Blennow, A Ivanoiu, et al.
AJNR. American Journal of Neuroradiology|December 24, 1997
Cerebral complications of murine monoclonal CD3 antibody (OKT3): CT and MR findingsP M Parizel, H W Snoeck, L van den Hauwe, et al.
Acta Neurologica Belgica|February 3, 2010
Organisation of inhospital acute stroke care and minimum criteria for stroke care units. Recommendations of the Belgian Stroke Council, V Thijs, A Peeters, et al.
American Journal of Medical Genetics|February 27, 2001
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examinationS A Irwin, B Patel, M Idupulapati, et al.
Pageof 12

Showing results (101-110 of 119) with videos related to

Sort By:
Pageof 12
Nature Genetics|June 1, 1992
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the beta-amyloid precursor protein geneL Hendriks, C M van Duijn, P Cras, et al.
Neurology|October 8, 2008
Progranulin variability has no major role in Parkinson disease genetic etiologyK Nuytemans, P Pals, K Sleegers, et al.
Acta Neuropathologica|October 1, 1998
Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala-->Gly mutationP Cras, F van Harskamp, L Hendriks, et al.
Annals of Neurology|November 15, 2001
Endocytic disturbances distinguish among subtypes of Alzheimer's disease and related disordersA Cataldo, G W Rebeck, B Ghetri, et al.
Brain : a Journal of Neurology|November 10, 2001
Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutationB Dermaut, S Kumar-Singh, C De Jonghe, et al.
Neurobiology of Disease|February 15, 2000
Behavioral disturbances without amyloid deposits in mice overexpressing human amyloid precursor protein with Flemish (A692G) or Dutch (E693Q) mutationS Kumar-Singh, I Dewachter, D Moechars, et al.
Neurology|May 20, 1999
Improved discrimination of AD patients using beta-amyloid(1-42) and tau levels in CSFF Hulstaert, K Blennow, A Ivanoiu, et al.
AJNR. American Journal of Neuroradiology|December 24, 1997
Cerebral complications of murine monoclonal CD3 antibody (OKT3): CT and MR findingsP M Parizel, H W Snoeck, L van den Hauwe, et al.
Acta Neurologica Belgica|February 3, 2010
Organisation of inhospital acute stroke care and minimum criteria for stroke care units. Recommendations of the Belgian Stroke Council, V Thijs, A Peeters, et al.
American Journal of Medical Genetics|February 27, 2001
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examinationS A Irwin, B Patel, M Idupulapati, et al.
Pageof 12