Genetic aspects of cerebrovascular disease

Secondary preventive medication persistence and adherence 1 year after stroke.

Neurology·2011

Worse blood pressure control in patients with cerebrovascular or peripheral arterial disease compared with coronary artery disease.

Journal of internal medicine·2010

Isolation of a cytochrome oxidase gene overexpressed in Alzheimer's disease brain.

Molecular and cellular neurosciences·2009

High cardiovascular event rates in patients with asymptomatic carotid stenosis: the REACH Registry.

European journal of neurology·2009

Current strategies for ischemic stroke prevention: role of multimodal combination therapies.

Journal of neurology·2007

Treatment of acute ischemic stroke.

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association·2007

Colchicine for Secondary Prevention After Stroke According to the Presence of Atherosclerosis.

Stroke·2026

Projection of Stroke Incidence and Costs in China: 2022 to 2050.

Stroke·2026

Thrombus Perviousness Is Associated With Differential Treatment Outcomes Following IVT and EVT in MeVO Stroke.

Stroke·2026

Intraarterial Thrombolysis: Past, Present, Future.

Stroke·2026

Colchicine for the Prevention of Vascular Events After an Acute Intracerebral Hemorrhage: A Placebo-Controlled Trial.

Stroke·2026

Standard Antiplatelet Therapy Versus Thrombolysis in Acute Spontaneous Spinal Cord Infarction: A Propensity Score-Matched Analysis.

Stroke·2026

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

American journal of medical genetics. Part A·2026

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Human mutation·2026

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

iScience·2026

Whole-genome and pan-genome analyses reveal genomic differences among nontypeable Haemophilus influenzae isolates from bronchiectasis, community-acquired pneumonia, and chronic obstructive pulmonary disease.

Frontiers in cellular and infection microbiology·2026

Characterisation of a Novel HLA-DQA1 Allele by Next Generation Sequencing: HLA-DQA1*01:03:13.

HLA·2026

CLUAP1 variants cause non-syndromic retinitis pigmentosa.

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie·2026

Related Experiment Videos

Genetic aspects of cerebrovascular disease

Related Concept Videos

Secondary preventive medication persistence and adherence 1 year after stroke.

Worse blood pressure control in patients with cerebrovascular or peripheral arterial disease compared with coronary artery disease.

Isolation of a cytochrome oxidase gene overexpressed in Alzheimer's disease brain.

High cardiovascular event rates in patients with asymptomatic carotid stenosis: the REACH Registry.

Current strategies for ischemic stroke prevention: role of multimodal combination therapies.

Treatment of acute ischemic stroke.

Colchicine for Secondary Prevention After Stroke According to the Presence of Atherosclerosis.

Projection of Stroke Incidence and Costs in China: 2022 to 2050.

Thrombus Perviousness Is Associated With Differential Treatment Outcomes Following IVT and EVT in MeVO Stroke.

Intraarterial Thrombolysis: Past, Present, Future.

Colchicine for the Prevention of Vascular Events After an Acute Intracerebral Hemorrhage: A Placebo-Controlled Trial.

Standard Antiplatelet Therapy Versus Thrombolysis in Acute Spontaneous Spinal Cord Infarction: A Propensity Score-Matched Analysis.

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

Whole-genome and pan-genome analyses reveal genomic differences among nontypeable Haemophilus influenzae isolates from bronchiectasis, community-acquired pneumonia, and chronic obstructive pulmonary disease.

Characterisation of a Novel HLA-DQA1 Allele by Next Generation Sequencing: HLA-DQA1*01:03:13.

CLUAP1 variants cause non-syndromic retinitis pigmentosa.

Related Experiment Videos

Genetic aspects of cerebrovascular disease

Related Concept Videos

Related Articles