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Neuroscience Letters
|
January 22, 2000
Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease
L Lilius, S Froelich Fabre, H Basun, et al.
Acta Neurologica Scandinavica
|
October 12, 2016
Primary familial brain calcification linked to deletion of 5' noncoding region of SLC20A2
P Pasanen, J Mäkinen, L Myllykangas, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences
|
March 1, 1997
Heritability for Alzheimer's disease: the study of dementia in Swedish twins
M Gatz, N L Pedersen, S Berg, et al.
Neurology
|
September 4, 2009
Follow-up of [11C]PIB uptake and brain volume in patients with Alzheimer disease and controls
N M Scheinin, S Aalto, J Koikkalainen, et al.
Neuroscience Letters
|
March 14, 2000
Interaction between estrogen receptor 1 and the epsilon4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women
K M Mattila, K Axelman, J O Rinne, et al.
Brain : a Journal of Neurology
|
June 28, 2008
PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease
J Koivunen, A Verkkoniemi, S Aalto, et al.
Alzheimer Disease and Associated Disorders
|
October 15, 1998
Long-term tacrine treatment in three mild Alzheimer patients: effects on nicotinic receptors, cerebral blood flow, glucose metabolism, EEG, and cognitive abilities
A Nordberg, K Amberla, M Shigeta, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
June 27, 2013
[11C]PIB, [18F]FDG and MR imaging in patients with mild cognitive impairment
A Brück, J R Virta, J Koivunen, et al.
Forensic Science International
|
December 17, 1998
Alzheimer changes are common in aged drivers killed in single car crashes and at intersections
M Viitanen, K Johansson, N Bogdanovic, et al.
Stroke
|
August 4, 2001
Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation
S Tuominen, V Juvonen, K Amberla, et al.
Page
of 17
Search research articles
Search
Showing results (151-160 of 167) with videos related to
Sort By:
Page
of 17
Neuroscience Letters
|
January 22, 2000
Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease
L Lilius, S Froelich Fabre, H Basun, et al.
Acta Neurologica Scandinavica
|
October 12, 2016
Primary familial brain calcification linked to deletion of 5' noncoding region of SLC20A2
P Pasanen, J Mäkinen, L Myllykangas, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences
|
March 1, 1997
Heritability for Alzheimer's disease: the study of dementia in Swedish twins
M Gatz, N L Pedersen, S Berg, et al.
Neurology
|
September 4, 2009
Follow-up of [11C]PIB uptake and brain volume in patients with Alzheimer disease and controls
N M Scheinin, S Aalto, J Koikkalainen, et al.
Neuroscience Letters
|
March 14, 2000
Interaction between estrogen receptor 1 and the epsilon4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women
K M Mattila, K Axelman, J O Rinne, et al.
Brain : a Journal of Neurology
|
June 28, 2008
PET amyloid ligand [11C]PIB uptake shows predominantly striatal increase in variant Alzheimer's disease
J Koivunen, A Verkkoniemi, S Aalto, et al.
Alzheimer Disease and Associated Disorders
|
October 15, 1998
Long-term tacrine treatment in three mild Alzheimer patients: effects on nicotinic receptors, cerebral blood flow, glucose metabolism, EEG, and cognitive abilities
A Nordberg, K Amberla, M Shigeta, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
June 27, 2013
[11C]PIB, [18F]FDG and MR imaging in patients with mild cognitive impairment
A Brück, J R Virta, J Koivunen, et al.
Forensic Science International
|
December 17, 1998
Alzheimer changes are common in aged drivers killed in single car crashes and at intersections
M Viitanen, K Johansson, N Bogdanovic, et al.
Stroke
|
August 4, 2001
Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation
S Tuominen, V Juvonen, K Amberla, et al.
Page
of 17