CR was not associated with hippocampal GM MD and hippocampal GM volume. 5 key findings →
Participants: 38 Evidence: low
Full summary, score breakdown and related studies → Original source
27,380 Alzheimer's and dementia studies in plain English, each scored out of 100.
CR was not associated with hippocampal GM MD and hippocampal GM volume. 5 key findings →
Participants: 38 Evidence: low
Full summary, score breakdown and related studies → Original source
Compared to ADSAA-, ADSAA+ showed putamen SRP hypermetabolism and middle occipital gyrus (MOG) SUVR hypometabolism. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
An MCI-like hypometabolic pattern was documented in 5 patients (7%) by SVA and 7 patients (10%) by SPM analysis; however, only 2 of these patients were selected by both methods. 4 key findings →
Participants: 71 Evidence: low
Full summary, score breakdown and related studies → Original source
Biological aging is the correlated decline of multi-organ system integrity central to the etiology of many age-related diseases. 3 key findings →
Evidence: moderate
Full summary, score breakdown and related studies → Original source
As our brains age, we tend to experience cognitive decline and are at greater risk of neurodegenerative disease and dementia. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Activity of the glymphatic system may be evaluated with diffusion images. 2 key findings →
Participants: 31 Evidence: low
Full summary, score breakdown and related studies → Original source
Alzheimer's disease(AD) is being the burden of society and family. 2 key findings →
Evidence: moderate
Full summary, score breakdown and related studies → Original source
DTI revealed significant differences in white matter diffusivity between CCD and cognitively healthy aged dogs. 5 key findings →
Participants: 20 Evidence: low
Full summary, score breakdown and related studies → Original source
Preserved executive functioning (EF) is crucial for daily functioning in the elderly and it appears to predict dementia development. 1 key finding →
Evidence: low
Full summary, score breakdown and related studies → Original source
Higher educational attainment is observationally associated with lower risk of Alzheimer's disease. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Studies of neurodegenerative disease risk in gout are contradictory. 1 key finding →
Evidence: low
Full summary, score breakdown and related studies → Original source
Cognitive reserve (CR) explains interindividual differences in the ability to maintain cognitive function in the presence of neuropathology. 2 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
The amygdala is composed of multiple nuclei with unique functions and connections in the limbic system and to the rest of the brain. 1 key finding →
Evidence: low
Full summary, score breakdown and related studies → Original source
White matter changes in patients with Alzheimer's disease are likely to be secondary to wallerian degeneration of fibre tracts due to neuronal loss in cortical associative areas. 3 key findings →
Participants: 16 Evidence: low
Full summary, score breakdown and related studies → Original source
Diffusion tensor imaging (DTI) can detect, in vivo, the directionality of molecular diffusion and estimate the microstructural integrity of white matter (WM) tracts. 1 key finding →
Participants: 14 Evidence: low
Full summary, score breakdown and related studies → Original source
Alzheimer's disease (AD) is characterized by a heterogeneous distribution of pathological changes throughout the brain. 2 key findings →
Participants: 36 Evidence: low
Full summary, score breakdown and related studies → Original source
Distinct patterns of brain atrophy exist in CBDS and PSP that can be used to differentiate the 2 diseases. 4 key findings →
Participants: 15 Evidence: low
Full summary, score breakdown and related studies → Original source
Our results indicated that higher global Aβ-SUVR was associated with higher mean diffusivity (MD) in the entire CN group (p = 0.023), and with both higher MD (p = 0.015) and lower fractional anisotropy (FA) (p = 0.026) in APOEɛ4 carriers. 4 key findings →
Evidence: moderate
Full summary, score breakdown and related studies → Original source
In the course of AD, the volume of the medial group nuclei, especially the mediodorsal medial magnocellular (MDm) nucleus, decreases. 4 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
There is increasing evidence showing that brain atrophy varies between patients with Alzheimer's disease (AD), suggesting that different anatomical patterns might exist within the same disorder. 4 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Early diagnosis of mild cognitive impairment (MCI) fascinates screening high-risk Alzheimer's disease (AD). 2 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
The volumes of the presubiculum and subiculum presented the most remarkable reduction in the patient's groups. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
Apathy severity was significantly associated with cortical thinning of the lateral parts of the right sided frontal, temporal and parietal lobes. 4 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
The contribution of cerebellar pathology to cognitive and behavioural manifestations is increasingly recognised, but the cerebellar profiles of FTD phenotypes are relatively poorly characterised. 4 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
3D MRE of the brain can be performed reproducibly and demonstrates significantly reduced brain tissue stiffness in patients with AD. 5 key findings →
Evidence: low
Full summary, score breakdown and related studies → Original source
9 of the 171 studies in this tag, picked by a fixed rule (a hash of each study's address), not by score or date; each page of this list shows a different 9. The same 9 appear here every time.
Free full text links and the Full text may need a subscription label come from Unpaywall, Europe PMC and OpenAlex records of free copies, checked 10 Oct 2026. A study with neither is unknown, not paywalled. Show only studies that are free to read
This is alzhub's own score. It is not an official metric, not an impact factor, and no journal, publisher or ranking body endorses it. We built it so that a reader who is not a scientist can tell a landmark trial from a conference abstract without having to already know the difference. Every point comes from one of 20 components, all of them printed on the study itself, so you can disagree with our arithmetic rather than having to trust the total.
Journals are placed in ordered tiers, never given a numeric impact factor — we could not verify current impact factors from a source we control, and an invented one would be worse than none. Tier 1 is the top-tier general journals (NEJM, The Lancet, JAMA, Nature, Science, Nature Medicine); tier 2 is the leading specialty journals; tier 3 is every other peer-reviewed journal. A separate part scores how much the journal's own papers are cited, which tells the tier-3 journals apart.
Two rules we don't bend. First, we never fill in a missing value: if a record does not state a sample size or a design, that component scores zero, and if we simply have no data for a part, such as a citation count, that part is left out and the study is scored on the parts we could check. The study card says which. Second, anything that is not a peer-reviewed article is capped at 16/100 and carries a warning chip — so a conference abstract or a company press release can never outrank a peer-reviewed paper, no matter how good it looks.
We rank a rigorous null result — a good trial showing that something does not work — above an early positive finding. Someone deciding whether to buy a supplement is served by that, and the rigour is already counted by the design and journal components.
The score is computed from the published data alone and is reproducible: the same file always yields the same numbers.
See the whole rubric drawn out → — four charts covering all 27,380 studies: how the scores are spread and where the cap bites, which of the 20 components the library is strong and weak on, which subjects rest on stronger evidence, and what kinds of study each subject is actually built from.
This is a large sample of the Alzheimer's literature, not an exhaustive index of it. It holds 27,380 records, built mostly from automated pulls of Europe PMC (60.6% of the library) and OpenAlex (18.6%), plus smaller pulls from PubMed, Crossref and medRxiv. If a study, a drug, or a finding isn't here, that is not evidence it doesn't exist in the literature — it may simply not have been pulled in yet.
1,032 records (3.8% of the library) are not peer-reviewed — 962 of those are preprints posted before any journal review, and the rest are conference abstracts, regulatory notices and reports. Every study card on this page states its status plainly, and the score above is capped for anything that isn't a peer-reviewed article.
See the full, machine-readable breakdown of this library's coverage →