Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M N Rossor

Showing results (121-130 of 216) with videos related to

Pageof 22
Sort By:
European Journal of Neurology|June 28, 2007
A novel presenilin 1 deletion (p.L166del) associated with early onset familial Alzheimer's diseaseW D Knight, J Kennedy, S Mead, et al.
Neurology|November 28, 2001
Rates of global and regional cerebral atrophy in AD and frontotemporal dementiaD Chan, N C Fox, R Jenkins, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2005
The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion diseaseR J Cordery, K Alner, L Cipolotti, et al.
Neurology|September 1, 1995
Frontal lobe or 'nonspecific' dementias are genetically heterogeneousA Ashworth, J Brown, S Gydesen, et al.
Archives of General Psychiatry|May 1, 1987
Age and histopathologic heterogeneity in Alzheimer's disease. Evidence for subtypesW Bondareff, C Q Mountjoy, M Roth, et al.
Neuroradiology|April 7, 2006
Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopyA D Waldman, R J Cordery, D G MacManus, et al.
Neurology|May 12, 2004
EEG abnormalities in frontotemporal lobar degenerationD Chan, R J Walters, E L Sampson, et al.
Neurology|July 13, 2005
Measuring atrophy in Alzheimer disease: a serial MRI study over 6 and 12 monthsJ M Schott, S L Price, C Frost, et al.
Neurology|March 1, 2006
A second family with familial AD and the V717L APP mutation has a later age at onsetA K Godbolt, J A Beck, J C Collinge, et al.
Neuropsychologia|April 9, 2008
Neuropsychological correlates of whole brain atrophy in Alzheimer's diseaseJ M Schott, S J Crutch, C Frost, et al.
Pageof 22

Showing results (121-130 of 216) with videos related to

Sort By:
Pageof 22
European Journal of Neurology|June 28, 2007
A novel presenilin 1 deletion (p.L166del) associated with early onset familial Alzheimer's diseaseW D Knight, J Kennedy, S Mead, et al.
Neurology|November 28, 2001
Rates of global and regional cerebral atrophy in AD and frontotemporal dementiaD Chan, N C Fox, R Jenkins, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2005
The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion diseaseR J Cordery, K Alner, L Cipolotti, et al.
Neurology|September 1, 1995
Frontal lobe or 'nonspecific' dementias are genetically heterogeneousA Ashworth, J Brown, S Gydesen, et al.
Archives of General Psychiatry|May 1, 1987
Age and histopathologic heterogeneity in Alzheimer's disease. Evidence for subtypesW Bondareff, C Q Mountjoy, M Roth, et al.
Neuroradiology|April 7, 2006
Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopyA D Waldman, R J Cordery, D G MacManus, et al.
Neurology|May 12, 2004
EEG abnormalities in frontotemporal lobar degenerationD Chan, R J Walters, E L Sampson, et al.
Neurology|July 13, 2005
Measuring atrophy in Alzheimer disease: a serial MRI study over 6 and 12 monthsJ M Schott, S L Price, C Frost, et al.
Neurology|March 1, 2006
A second family with familial AD and the V717L APP mutation has a later age at onsetA K Godbolt, J A Beck, J C Collinge, et al.
Neuropsychologia|April 9, 2008
Neuropsychological correlates of whole brain atrophy in Alzheimer's diseaseJ M Schott, S J Crutch, C Frost, et al.
Pageof 22