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Lack of association of very low density lipoprotein receptor gene polymorphism with Caucasian Alzheimer's disease. [electronic resource] by
- Okuizumi, K
- Onodera, O
- Seki, K
- Tanaka, H
- Namba, Y
- Ikeda, K
- Saunders, A M
- Pericak-Vance, M A
- Roses, A D
- Tsuji, S
Producer: 19961016
In:
Annals of neurology vol. 40
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Utility of the apolipoprotein E genotype in the diagnosis of Alzheimer's disease. Alzheimer's Disease Centers Consortium on Apolipoprotein E and Alzheimer's Disease. [electronic resource] by
- Mayeux, R
- Saunders, A M
- Shea, S
- Mirra, S
- Evans, D
- Roses, A D
- Hyman, B T
- Crain, B
- Tang, M X
- Phelps, C H
Producer: 19980219
In:
The New England journal of medicine vol. 338
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Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases. [electronic resource] by
- Saunders, A M
- Schmader, K
- Breitner, J C
- Benson, M D
- Brown, W T
- Goldfarb, L
- Goldgaber, D
- Manwaring, M G
- Szymanski, M H
- McCown, N
Producer: 19931008
In:
Lancet (London, England) vol. 342
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115.
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Cis-acting human ApoE tissue expression element is associated with human pattern of intraneuronal ApoE in transgenic mice. [electronic resource] by
- Roses, A D
- Gilbert, J
- Xu, P T
- Sullivan, P
- Popko, B
- Burkhart, D S
- Christian-Rothrock, T
- Saunders, A M
- Maeda, N
- Schmechel, D E
Producer: 19980612
In:
Neurobiology of aging vol. 19
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116.
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Rosiglitazone does not improve cognition or global function when used as adjunctive therapy to AChE inhibitors in mild-to-moderate Alzheimer's disease: two phase 3 studies. [electronic resource] by
- Harrington, C
- Sawchak, S
- Chiang, C
- Davies, J
- Donovan, C
- Saunders, A M
- Irizarry, M
- Jeter, B
- Zvartau-Hind, M
- van Dyck, C H
- Gold, M
Producer: 20111205
In:
Current Alzheimer research vol. 8
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119.
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Hypothesis: microtubule instability and paired helical filament formation in the Alzheimer disease brain are related to apolipoprotein E genotype. [electronic resource] by
- Strittmatter, W J
- Weisgraber, K H
- Goedert, M
- Saunders, A M
- Huang, D
- Corder, E H
- Dong, L M
- Jakes, R
- Alberts, M J
- Gilbert, J R
Producer: 19940323
In:
Experimental neurology vol. 125
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120.
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Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms. [electronic resource] by
- Mastaglia, F L
- Rojana-udomsart, A
- James, I
- Needham, M
- Day, T J
- Kiers, L
- Corbett, J A
- Saunders, A M
- Lutz, M W
- Roses, A D
Producer: 20140724
In:
Neuromuscular disorders : NMD vol. 23
Availability: No items available.
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