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swedish
5 studies tagged swedish, dated 1995-12-01 to 2022-10-19. Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Synaptogenic effect of APP-Swedish mutation in familial Alzheimer's disease 2022-10-19
- Dementia Diagnosis Is Associated with Changes in Antidiabetic Drug Prescription: An Open-Cohort Study of ∼130,000 Swedish Subjects over 14 Years 2020-01-01
- Vitamin D deficiency was common among nursing home residents and associated with dementia: a cross sectional study of 545 Swedish nursing home residents 2017-10-10
Studies
5 studies carry this tag.
Date range
1995 to 2022
Top journals
- BMC geriatrics 1
- European journal of human genetics : EJHG 1
- Journal of Alzheimer's disease : JAD 1
- Nature medicine 1
- Science translational medicine 1
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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Mutations in β-amyloid (Aβ) precursor protein ( APP ) cause familial Alzheimer's disease (AD) probably by enhancing Aβ peptides production from APP.
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Dementia patients had lower probability of receiving newer antidiabetic drugs, with simultaneous higher insulin dispensation compared to dementia-free subjects.
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Vitamin D deficiency was common among nursing home residents and strongly associated with dementia.
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Early-onset dominantly inherited forms of Alzheimer's disease (AD) are rare, but studies of such cases have revealed important information about the disease mechanisms.
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Several missense mutations causing early-onset Alzheimer's disease (AD) have been described in the gene coding for the beta-amyloid precursor protein (beta APP).