Found: 20
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Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites.
- Published in:
- Molecular Psychiatry, 2012, v. 17, n. 2, p. 223, doi. 10.1038/mp.2011.24
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- Publication type:
- Article
The association between human blood clot analogue computed tomography imaging, composition, contraction, and mechanical characteristics.
- Published in:
- PLoS ONE, 2023, v. 18, n. 11, p. 1, doi. 10.1371/journal.pone.0293456
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- Publication type:
- Article
Variable expression of presenilin 1 is not a major determinant of risk for late-onset Alzheimer's Disease.
- Published in:
- Journal of Neurology, 2001, v. 248, n. 11, p. 935, doi. 10.1007/s004150170044
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- Publication type:
- Article
Contribution of Red Blood Cells and Platelets to Blood Clot Computed Tomography Imaging and Compressive Mechanical Characteristics.
- Published in:
- Annals of Biomedical Engineering, 2024, v. 52, n. 8, p. 2151, doi. 10.1007/s10439-024-03515-y
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- Publication type:
- Article
Cholesterol and triglycerides moderate the effect of apolipoprotein E on memory functioning in older adults.
- Published in:
- 2007
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- Publication type:
- Journal Article
Reduced functional brain activity response in cognitively intact apolipoprotein E epsilon4 carriers.
- Published in:
- 2006
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- Publication type:
- Journal Article
Familial clustering and genetic risk for dementia in a genetically isolated Dutch population.
- Published in:
- Brain: A Journal of Neurology, 2004, v. 127, n. 7, p. 1641, doi. 10.1093/brain/awh179
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- Publication type:
- Article
Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation.
- Published in:
- 2001
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- Publication type:
- journal article
Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation.
- Published in:
- 2000
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- Publication type:
- journal article
Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692).
- Published in:
- 2000
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- Publication type:
- journal article
A novel presenilin 1 mutation associated with Pick's disease but not ß-amyloid plaques.
- Published in:
- 2004
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- Publication type:
- Journal Article
PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease.
- Published in:
- 2003
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- Publication type:
- Journal Article
Granulin mutations associated with frontotemporal lobar degeneration and related disorders: An update.
- Published in:
- 2008
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- Publication type:
- Other
Progranulin locus deletion in frontotemporal dementia.
- Published in:
- Human Mutation, 2008, v. 29, n. 1, p. 53, doi. 10.1002/humu.20651
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- Publication type:
- Article
Alzheimer dementia caused by a novel mutation located in the APP C-terminal intracytosolic fragment.
- Published in:
- Human Mutation, 2006, v. 27, n. 9, p. 888, doi. 10.1002/humu.20402
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- Publication type:
- Article
The role of tau ( MAPT) in frontotemporal dementia and related tauopathies.
- Published in:
- Human Mutation, 2004, v. 24, n. 4, p. 277, doi. 10.1002/humu.20086
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- Publication type:
- Article
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.
- Published in:
- Molecular Psychiatry, 2002, v. 7, n. 10, p. 1064, doi. 10.1038/sj.mp.4001198
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- Publication type:
- Article
Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family.
- Published in:
- 2004
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- Publication type:
- Letter
Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe(Communicated by Richard G.H. Cotton).
- Published in:
- Human Mutation, 2003, v. 22, n. 5, p. 409, doi. 10.1002/humu.10269
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- Publication type:
- Article
Dinucleotide repeat polymorphism at the D21S258 locus.
- Published in:
- Human Molecular Genetics, 1992, v. 1, n. 6, p. 449
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- Publication type:
- Article