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- 2024
-
Mark
Efficacy assessment of an active tau immunotherapy in Alzheimer's disease patients with amyloid and tau pathology : a post hoc analysis of the “ADAMANT” randomised, placebo-controlled, double-blind, multi-centre, phase 2 clinical trial
(
- Contribution to journal › Article
-
Mark
European stroke organisation (ESO) guideline on cerebral small vessel disease, part 2, lacunar ischaemic stroke
2024) In European Stroke Journal(
- Contribution to journal › Article
- 2021
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Mark
Excessive White Matter Hyperintensity Increases Susceptibility to Poor Functional Outcomes After Acute Ischemic Stroke
(
- Contribution to journal › Article
- 2020
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Mark
White matter hyperintensity burden in acute stroke patients differs by ischemic stroke subtype
(
- Contribution to journal › Article
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Mark
Brain Volume : An Important Determinant of Functional Outcome After Acute Ischemic Stroke
(
- Contribution to journal › Article
- 2019
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Mark
Genome-wide association study of cerebral small vessel disease reveals established and novel loci
(
- Contribution to journal › Article
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Mark
White matter hyperintensity quantification in large-scale clinical acute ischemic stroke cohorts – The MRI-GENIE study
(
- Contribution to journal › Article
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Mark
Big Data Approaches to Phenotyping Acute Ischemic Stroke Using Automated Lesion Segmentation of Multi-Center Magnetic Resonance Imaging Data
(
- Contribution to journal › Article
- 2017
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Mark
Dolichoectasia and Small Vessel Disease in Young Patients with Transient Ischemic Attack and Stroke
(
- Contribution to journal › Article
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Mark
Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke
(
- Contribution to journal › Article
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Mark
Design and rationale for examining neuroimaging genetics in ischemic stroke : The MRI-GENIE study
(
- Contribution to journal › Article
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Mark
Genetic variation at 16q24.2 is associated with small vessel stroke
(
- Contribution to journal › Article
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Mark
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
(
- Contribution to journal › Article
- 2016
-
Mark
Reproducibility and variability of quantitative magnetic resonance imaging markers in cerebral small vessel disease
(
- Contribution to journal › Scientific review
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Mark
METACOHORTS for the study of vascular disease and its contribution to cognitive decline and neurodegeneration : An initiative of the Joint Programme for Neurodegenerative Disease Research
(
- Contribution to journal › Article
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Mark
Genetic variants in CETP increase risk of intracerebral hemorrhage
(
- Contribution to journal › Article
- 2015
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Mark
Clinically Relevant Depressive Symptoms in Young Stroke Patients - Results of the sifap1 Study
(
- Contribution to journal › Article
-
Mark
Family History in Young Patients With Stroke.
(
- Contribution to journal › Article
-
Mark
Brain Magnetic Resonance Imaging Findings Fail to Suspect Fabry Disease in Young Patients With an Acute Cerebrovascular Event.
(
- Contribution to journal › Article
-
Mark
Recommendations from the international stroke genetics consortium, part 1: standardized phenotypic data collection.
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease
(
- Contribution to journal › Article
- 2014
-
Mark
Clinical signs in young patients with stroke related to FAST: results of the sifap1 study.
(
- Contribution to journal › Article
-
Mark
Pathogenic Ischemic Stroke Phenotypes in the NINDS-Stroke Genetics Network.
(
- Contribution to journal › Article
-
Mark
Meta-Analysis of Genome-Wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage.
(
- Contribution to journal › Article
- 2013
-
Mark
MRI in acute cerebral ischemia of the young: The Stroke in Young Fabry Patients (sifap1) Study.
(
- Contribution to journal › Article
-
Mark
Novel Insights Into the Genetics of Intracerebral Hemorrhage
(
- Contribution to journal › Article
-
Mark
Acute Cerebrovascular Disease in the Young The Stroke in Young Fabry Patients Study
(
- Contribution to journal › Article
-
Mark
Common Variants Within Oxidative Phosphorylation Genes Influence Risk of Ischemic Stroke and Intracerebral Hemorrhage
(
- Contribution to journal › Article
-
Mark
Heritability Estimates Identify a Substantial Genetic Contribution to Risk and Outcome of Intracerebral Hemorrhage
(
- Contribution to journal › Article
-
Mark
Stroke Genetics Network (SiGN) Study: Design and Rationale for a Genome-Wide Association Study of Ischemic Stroke Subtypes.
(
- Contribution to journal › Article
- 2012
-
Mark
Kidney Function and White Matter Disease in Young Stroke Patients Analysis of the Stroke in Young Fabry Patients Study Population
(
- Contribution to journal › Article
-
Mark
Burden of Risk Alleles for Hypertension Increases Risk of Intracerebral Hemorrhage
(
- Contribution to journal › Article
-
Mark
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
(
- Contribution to journal › Article
- 2011
-
Mark
Protocol and Methodology of the Stroke in Young Fabry Patients (sifap1) Study: A Prospective Multicenter European Study of 5,024 Young Stroke Patients Aged 18-55 Years
(
- Contribution to journal › Article
-
Mark
APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
(
- Contribution to journal › Article
- 2010
-
Mark
Variants at APOE Influence Risk of Deep and Lobar Intracerebral Hemorrhage
(
- Contribution to journal › Article
- 2009
-
Mark
International Validation of a Computerized Algorithm for Etiologic Classification of Ischemic Stroke: The Causative Classification of Stroke System
2009) International Stroke Conference 2009 In Stroke: a journal of cerebral circulation 40(4). p.203-203(
- Contribution to journal › Published meeting abstract
- 2008
-
Mark
The EUROclass trial: defining subgroups in common variable immunodeficiency.
(
- Contribution to journal › Article