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Neurocase
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April 5, 2005
Knight's move thinking? Mild cognitive impairment in a chess player
H A Archer, J M Schott, J Barnes, et al.
Neurology
|
April 24, 2002
Neuropathologic variation in frontotemporal dementia due to the intronic tau 10(+16) mutation
P L Lantos, N J Cairns, M N Khan, et al.
Neurology
|
March 15, 2006
MRS shows abnormalities before symptoms in familial Alzheimer disease
A K Godbolt, A D Waldman, D G MacManus, et al.
Neuroscience Letters
|
December 31, 2002
Cerebrospinal fluid S100B correlates with brain atrophy in Alzheimer's disease
A Petzold, R Jenkins, H C Watt, et al.
Brain : a Journal of Neurology
|
June 1, 1992
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features
J Collinge, J Brown, J Hardy, et al.
International Journal of Geriatric Psychiatry
|
September 16, 2006
Do symptoms of memory impairment correspond to cognitive impairment: a cross sectional study of a clinical cohort
H A Archer, F Macfarlane, S Price, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 18, 2003
Transient ischaemic attacks are associated with increased rates of global cerebral atrophy
R J L Walters, N C Fox, J M Schott, et al.
Neuropathology and Applied Neurobiology
|
August 8, 2001
Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic beta-amyloid pathology known as 'cotton wool' plaques
D M Mann, A Takeuchi, S Sato, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1989
Recommended minimum data to be collected in research studies on Alzheimer's disease. The MRC (UK) Alzheimer's Disease Workshop Steering Committee
G K Wilcock, R A Hope, D N Brooks, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 18, 2005
Mapping the onset and progression of atrophy in familial frontotemporal lobar degeneration
J C Janssen, J M Schott, L Cipolotti, et al.
Page
of 22
Search research articles
Search
Showing results (161-170 of 216) with videos related to
Sort By:
Page
of 22
Neurocase
|
April 5, 2005
Knight's move thinking? Mild cognitive impairment in a chess player
H A Archer, J M Schott, J Barnes, et al.
Neurology
|
April 24, 2002
Neuropathologic variation in frontotemporal dementia due to the intronic tau 10(+16) mutation
P L Lantos, N J Cairns, M N Khan, et al.
Neurology
|
March 15, 2006
MRS shows abnormalities before symptoms in familial Alzheimer disease
A K Godbolt, A D Waldman, D G MacManus, et al.
Neuroscience Letters
|
December 31, 2002
Cerebrospinal fluid S100B correlates with brain atrophy in Alzheimer's disease
A Petzold, R Jenkins, H C Watt, et al.
Brain : a Journal of Neurology
|
June 1, 1992
Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features
J Collinge, J Brown, J Hardy, et al.
International Journal of Geriatric Psychiatry
|
September 16, 2006
Do symptoms of memory impairment correspond to cognitive impairment: a cross sectional study of a clinical cohort
H A Archer, F Macfarlane, S Price, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 18, 2003
Transient ischaemic attacks are associated with increased rates of global cerebral atrophy
R J L Walters, N C Fox, J M Schott, et al.
Neuropathology and Applied Neurobiology
|
August 8, 2001
Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic beta-amyloid pathology known as 'cotton wool' plaques
D M Mann, A Takeuchi, S Sato, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 1, 1989
Recommended minimum data to be collected in research studies on Alzheimer's disease. The MRC (UK) Alzheimer's Disease Workshop Steering Committee
G K Wilcock, R A Hope, D N Brooks, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 18, 2005
Mapping the onset and progression of atrophy in familial frontotemporal lobar degeneration
J C Janssen, J M Schott, L Cipolotti, et al.
Page
of 22