Found: 47
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Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Monomicrobial Nonneutrocytic Bacterascites Due to Burkholderia pickettii.
- Published in:
- 1998
- By:
- Publication type:
- Letter
Using blood transcriptome analysis for Alzheimer's disease diagnosis and patient stratification.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 4, p. 2469, doi. 10.1002/alz.13691
- By:
- Publication type:
- Article
A blood‐based multi‐pathway biomarker assay for early detection and staging of Alzheimer's disease across ethnic groups.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 3, p. 2000, doi. 10.1002/alz.13676
- By:
- Publication type:
- Article
An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE‐ε4 in Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.064428
- By:
- Publication type:
- Article
Large-scale plasma proteomic profiling identifies a high-performance biomarker panel for Alzheimer’s disease screening and staging.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 1, p. 88, doi. 10.1002/alz.12369
- By:
- Publication type:
- Article
A high‐performance biomarker panel for Alzheimer's disease screening and staging identified by large‐scale plasma proteomic profiling.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.056099
- By:
- Publication type:
- Article
Blood transcriptome analysis for Alzheimer' disease in Hong Kong Chinese population.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.056643
- By:
- Publication type:
- Article
Deep learning for polygenic score analysis for Alzheimer's disease risk prediction in the Chinese population.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.056625
- By:
- Publication type:
- Article
Evaluation of genetic risk for Alzheimer's disease in the Hong Kong Chinese population: Genetics/genetic factors of Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.045142
- By:
- Publication type:
- Article
SORL1‐variant carriers in ADES‐ADSP: A higher level of variant pathogenicity associates with earlier age at onset of Alzheimer's disease: Genetics/genetic factors of Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.044492
- By:
- Publication type:
- Article
Exome sequencing identifies three novel AD‐associated genes: Genetics/genetic factors of Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.041592
- By:
- Publication type:
- Article
Reply to "Down Syndrome Cognitive Marker's Significance in Alzheimer's Disease and Dementia Management".
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, n. 9, p. 1238, doi. 10.1016/j.jalz.2019.05.003
- By:
- Publication type:
- Article
Cognitive markers of preclinical and prodromal Alzheimer's disease in Down syndrome.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, n. 2, p. 245, doi. 10.1016/j.jalz.2018.08.009
- By:
- Publication type:
- Article
P3‐104: IDENTIFICATION OF GENETIC RISK FACTORS FOR ALZHEIMER'S DISEASE IN THE CHINESE POPULATION.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1106, doi. 10.1016/j.jalz.2018.06.1461
- By:
- Publication type:
- Article
P2‐119: DEMENTIA AMONG THOSE WITH DOWN SYNDROME: FOCUSED ASSOCIATION STUDY ON TRISOMY 21 SNPS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P714, doi. 10.1016/j.jalz.2018.06.805
- By:
- Publication type:
- Article
O1‐08‐02: SEQUENCE OF COGNITIVE DECLINE IN ADULTS WITH DOWN SYNDROME DURING PROGRESSION FROM PRECLINICAL TO PRODROMAL ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P235, doi. 10.1016/j.jalz.2018.06.2373
- By:
- Publication type:
- Article
Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26280-1
- By:
- Publication type:
- Article
Plasma biomarkers for amyloid, tau, and cytokines in Down syndrome and sporadic Alzheimer's disease.
- Published in:
- Alzheimer's Research & Therapy, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13195-019-0477-0
- By:
- Publication type:
- Article
Neurofilament light as a blood biomarker for neurodegeneration in Down syndrome.
- Published in:
- Alzheimer's Research & Therapy, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13195-018-0367-x
- By:
- Publication type:
- Article
GENETIC DISSECTION OF SEVERITY AND ONSET MODULATORS FOR ALZHEIMER’S PATHOLOGY IN DOWN SYNDROME USING CELLULAR SYSTEMS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P998, doi. 10.1016/j.jalz.2017.06.1380
- By:
- Publication type:
- Article
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: Clinical, neuroanatomical and neuropathological features
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Non-coding variability at the APOE locus contributes to the Alzheimer's risk.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10945-z
- By:
- Publication type:
- Article
Editorial: Genetic and molecular diversity in Parkinson’s disease.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.1094914
- By:
- Publication type:
- Article
Homozygosity analysis in amyotrophic lateral sclerosis.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 12, p. 1429, doi. 10.1038/ejhg.2013.59
- By:
- Publication type:
- Article
Multi‐Omics‐Based Autophagy‐Related Untypical Subtypes in Patients with Cerebral Amyloid Pathology.
- Published in:
- Advanced Science, 2022, v. 9, n. 23, p. 1, doi. 10.1002/advs.202201212
- By:
- Publication type:
- Article
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.
- Published in:
- JAMA Neurology, 2020, v. 77, n. 6, p. 746, doi. 10.1001/jamaneurol.2020.0428
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- Publication type:
- Article
Association of Dementia With Mortality Among Adults With Down Syndrome Older Than 35 Years.
- Published in:
- JAMA Neurology, 2019, v. 72, n. 6, p. 152, doi. 10.1001/jamaneurol.2018.3616
- By:
- Publication type:
- Article
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers.
- Published in:
- Brain: A Journal of Neurology, 2014, v. 137, n. 9, p. 2480, doi. 10.1093/brain/awu179
- By:
- Publication type:
- Article
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 3, p. 736, doi. 10.1093/brain/awr361
- By:
- Publication type:
- Article
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 3, p. 751, doi. 10.1093/brain/awr365
- By:
- Publication type:
- Article
Aging related cognitive changes associated with Alzheimer's disease in Down syndrome.
- Published in:
- Annals of Clinical & Translational Neurology, 2018, v. 5, n. 6, p. 741, doi. 10.1002/acn3.571
- By:
- Publication type:
- Article
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotype.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 24, p. 5483, doi. 10.1093/hmg/ddw348
- By:
- Publication type:
- Article
Hong Kong's Cultural and Creative Industries During the Last Eight Years: Reflections on Their Relevance to the Employment Market.
- Published in:
- Journal of Youth Studies (10297847), 2009, v. 12, n. 2, p. 39
- By:
- Publication type:
- Article
Validation and application of health utilities index in Chinese subjects with down syndrome.
- Published in:
- Health & Quality of Life Outcomes, 2014, v. 12, n. 1, p. 1, doi. 10.1186/s12955-014-0144-x
- By:
- Publication type:
- Article
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions.
- Published in:
- Movement Disorders, 2022, v. 37, n. 8, p. 1593, doi. 10.1002/mds.29126
- By:
- Publication type:
- Article
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 4, p. 717, doi. 10.1007/s00401-019-02119-4
- By:
- Publication type:
- Article
Differential Associations of Apolipoprotein E ε4 Genotype With Attentional Abilities Across the Life Span of Individuals With Down Syndrome.
- Published in:
- JAMA Network Open, 2020, v. 3, n. 10, p. e2018221, doi. 10.1001/jamanetworkopen.2020.18221
- By:
- Publication type:
- Article
A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma.
- Published in:
- 2013
- By:
- Publication type:
- Abstract
Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat.
- Published in:
- Frontiers in Neurology, 2012, v. 3, p. 1, doi. 10.3389/fneur.2012.00136
- By:
- Publication type:
- Article
Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder--implications of a copy number variation involving DPP10.
- Published in:
- Molecular Autism, 2017, v. 8, p. 1, doi. 10.1186/s13229-017-0136-x
- By:
- Publication type:
- Article
Editorial: Genetics and biomarkers of Alzheimer's disease in Asian populations.
- Published in:
- Frontiers in Neuroscience, 2024, p. 1, doi. 10.3389/fnins.2024.1357783
- By:
- Publication type:
- Article
Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.
- Published in:
- Movement Disorders, 2014, v. 29, n. 2, p. 245, doi. 10.1002/mds.25732
- By:
- Publication type:
- Article
Identification of a novel THAP1 mutation at R29 amino-acid residue in sporadic patients with early-onset dystonia.
- Published in:
- Movement Disorders, 2009, v. 24, n. 16, p. 2428, doi. 10.1002/mds.22849
- By:
- Publication type:
- Article
A robust model for read count data in exome sequencing experiments and implications for copy number variant calling.
- Published in:
- Bioinformatics, 2012, v. 28, n. 21, p. 2747, doi. 10.1093/bioinformatics/bts526
- By:
- Publication type:
- Article