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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
- Published in:
- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01121-w
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- Article
A family‐based genetic study identifies mutations in TLR9 impairing receptor activation: A role for innate immunity in AD pathogenesis: Developing topics.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.047212
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- Article
Transcript analysis using long‐read sequencing reveals the complex splicing profile of AD‐associated gene ABCA7: Genetics: Genetics and omics of AD I.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.042815
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- Article
ABCA7 PTC mutation carriers present with Alzheimer's disease pathology and cerebral amyloid angiopathy: Basic science and pathogenesis: Genetics and omics of AD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.041513
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- Article
ABCA7 mutations are major contributors to Alzheimer's disease in Belgian patients: Genetics/genetic factors of Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.040227
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- Article
Recessive missense variants in VWA2 increase risk of developing Alzheimer's disease: Genetics/molecular genetics.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.039791
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- Article
O3‐13‐03: THE ROLE OF ZCWPW1 SUSCEPTIBILITY LOCUS RARE VARIANTS IN ALZHEIMER'S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P920, doi. 10.1016/j.jalz.2019.06.4698
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- Article
Amyloid-β<sub>1–43</sub> cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations.
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- Alzheimer's Research & Therapy, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13195-020-00676-5
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- Article
Genotype‐phenotype of PSEN1 p.CYS263PHE carriers in Flanders‐Belgian Alzheimer's disease patients.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.055244
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- Article
Rare missense mutations and compound heterozygous mutations in ABCA7 contribute to Alzheimer's disease in Belgian patients.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.051341
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- Article