Genetics of vascular dementia - review from the ICVD working group. - Test2 - elhamkhani - TriplyDB

Genetics of vascular dementia - review from the ICVD working group.

Genetics of vascular dementia - review from the ICVD working group.

http://www.wikidata.org/entity/Q30235432

about

Potential Therapeutics for Vascular Cognitive Impairment and Dementia.GWAS on family history of Alzheimer's disease.The more critical murderer of atherosclerosis than lipid metabolism: chronic stress.

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Genetics of vascular dementia - review from the ICVD working group.

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2017 nî lūn-bûn

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2017 թուականի Մարտին հրատարակուած գիտական յօդուած

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2017 թվականի մարտին հրատարակված գիտական հոդված

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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Genetics of vascular dementia - review from the ICVD working group.

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Genetics of vascular dementia - review from the ICVD working group.

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Genetics of vascular dementia - review from the ICVD working group.

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Genetics of vascular dementia - review from the ICVD working group.

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Genetics of vascular dementia - review from the ICVD working group.

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Genetics of vascular dementia - review from the ICVD working group.

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Genetics of vascular dementia - review from the ICVD working group.

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Helena Schmidt

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Hieab H H Adams

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Lefkos Middleton

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Raquel Manso-Calderón

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Saima Siddiqi

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Creative Commons Attribution 4.0 International

P2860

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

A TGF-beta 1 polymorphism association with dementia and neuropathologies: the HAAS

Neuroimaging in vascular cognitive impairment: a state-of-the-art review

Shifting the CARASIL paradigm: report of a non-Asian family and literature review

White Matter Lesion Progression: Genome-Wide Search for Genetic Influences

Association of intronic sequence variant in the gene encoding spleen tyrosine kinase with susceptibility to vascular dementia

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.

Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification.

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