Found: 14
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A novel human pain insensitivity disorder caused by a point mutation in ZFHX2.
- Published in:
- 2018
- By:
- Publication type:
- journal article
P4‐240: STOP‐GAIN VARIANT IN MICROGLIA‐EXPRESSED GENE GMIP IS ASSOCIATED WITH EARLY‐ONSET ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1534, doi. 10.1016/j.jalz.2018.07.061
- By:
- Publication type:
- Article
P3‐077: ALZHEIMER'S DISEASE (AD) POLYGENIC RISK SCORE (PRS) AS A PREDICTOR OF CONVERSION FROM MILD COGNITIVE IMPAIRMENT (MCI).
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1094, doi. 10.1016/j.jalz.2018.06.1433
- By:
- Publication type:
- Article
P1‐168: LINKING POLYGENIC RISK SCORES TO ALZHEIMER'S DISEASE GENES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P342, doi. 10.1016/j.jalz.2018.06.172
- By:
- Publication type:
- Article
MULTI-INFARCT DEMENTIA OF SWEDISH TYPE IS CAUSED BY 3’UTR COL4A1 MUTATION.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P973, doi. 10.1016/j.jalz.2017.06.1312
- By:
- Publication type:
- Article
NOVEL CANDIDATE GENES FOR DEMENTIA WITH LEWY BODIES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P977, doi. 10.1016/j.jalz.2017.06.1322
- By:
- Publication type:
- Article
INVESTIGATING GENETIC VARIATION IN ALZHEIMER’S DISEASE USING WHOLE-EXOME SEQUENCING.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P977, doi. 10.1016/j.jalz.2017.06.1323
- By:
- Publication type:
- Article
GENETICS OF DLB AND RELEVANCE FOR MECHANISMS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1444, doi. 10.1016/j.jalz.2017.07.478
- By:
- Publication type:
- Article
GENETIC CHARACTERIZATION OF A TURKISH DEMENTIA COHORT: FOCUS ON TYROBP.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1490, doi. 10.1016/j.jalz.2017.07.576
- By:
- Publication type:
- Article
CALCULATING POLYGENIC RISK FOR INDIVIDUALS WITH SPORADIC EARLY ONSET ALZHEIMER’S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P976, doi. 10.1016/j.jalz.2017.06.1321
- By:
- Publication type:
- Article
LINKAGE AND WHOLE GENOME SEQUENCE ANALYSIS OF ALZHEIMER'S DISEASE RESILIENCE AND RISK.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P675, doi. 10.1016/j.jalz.2016.06.1325
- By:
- Publication type:
- Article
INVESTIGATING SARM1 VARIANTS IN ALZHEIMER’S DISEASE COHORTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P855, doi. 10.1016/j.jalz.2016.06.1750
- By:
- Publication type:
- Article
An Aged Canid with Behavioral Deficits Exhibits Blood and Cerebrospinal Fluid Amyloid Beta Oligomers.
- Published in:
- Frontiers in Aging Neuroscience, 2018, p. 1, doi. 10.3389/fnagi.2018.00007
- By:
- Publication type:
- Article
CLN8 disease caused by large genomic deletions.
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 1, p. 85, doi. 10.1002/mgg3.263
- By:
- Publication type:
- Article