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المؤلفون: Rainer Malik, Kristiina Rannikmäe, Matthew Traylor, Stéphanie Debette, Cathie Sudlow, Muralidharan Sargurupremraj, Marios K. Georgakis, Hugh S. Markus, Jemma C. Hopewell, Martin Dichgans
المساهمون: Ludwig-Maximilians-Universität München (LMU), University of Edinburgh, Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), University of Cambridge [UK] (CAM), Traylor, Matthew [0000-0001-6624-8621], Apollo - University of Cambridge Repository
المصدر: Annals of Neurology
Annals of Neurology, Wiley, 2018, 84 (6), pp.934-939. ⟨10.1002/ana.25369⟩
Annals of neurology 84(6), 934-939 (2018). doi:10.1002/ana.25369مصطلحات موضوعية: 0301 basic medicine, Collagen Type IV, statistics & numerical data [Databases, Factual], Databases, Factual, Nitric Oxide Synthase Type III, [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, Single-nucleotide polymorphism, Genome-wide association study, genetics [Protein Serine-Threonine Kinases], Biology, Protein Serine-Threonine Kinases, Brief Communication, genetics [Protein-Serine-Threonine Kinases], 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Polymorphism (computer science), Risk Factors, Mendelian randomization, Genetic variation, medicine, genetics [Protein-Tyrosine Kinases], Humans, Genetic Predisposition to Disease, ddc:610, genetics [Collagen Type IV], Allele frequency, Stroke, Genetics, [SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE], Mendelian Randomization Analysis, genetics [Nitric Oxide Synthase Type III], COL4A1 protein, human, Protein-Tyrosine Kinases, medicine.disease, Protein-Serine-Threonine Kinases, Dyrk kinase, Europe, 030104 developmental biology, Neurology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, genetics [Stroke], Neurology (clinical), NOS3 protein, human, Brief Communications, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf
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المؤلفون: Horst Urbach, Sebastian Paus, Marcus Grobe-Einsler
المصدر: Journal of stroke and cerebrovascular diseases 29(12), 105386 (2020). doi:10.1016/j.jstrokecerebrovasdis.2020.105386
مصطلحات موضوعية: Male, genetics [Leukoencephalopathies], Pontine stroke, CADASIL, Leukoencephalopathy, 0302 clinical medicine, Recurrence, therapy [Cerebral Small Vessel Diseases], Medicine, therapy [Brain Stem Infarctions], genetics [Collagen Type IV], Stroke, diagnostic imaging [Brain Stem Infarctions], PADMAL, Rehabilitation, blood supply [Pons], medicine.anatomical_structure, Cardiology, Disease Progression, diagnostic imaging [Leukoencephalopathies], diagnostic imaging [Cerebral Small Vessel Diseases], Cardiology and Cardiovascular Medicine, Vasculitis, Adult, Collagen Type IV, medicine.medical_specialty, COL4A1, Central nervous system, physiopathology [Brain Stem Infarctions], 03 medical and health sciences, Internal medicine, Humans, Genetic Predisposition to Disease, ddc:610, physiopathology [Cerebral Small Vessel Diseases], physiopathology [Leukoencephalopathies], business.industry, Microangiopathy, COL4A1 protein, human, medicine.disease, Pons, Hyperintensity, genetics [Brain Stem Infarctions], therapy [Leukoencephalopathies], Mutation, genetics [Cerebral Small Vessel Diseases], Surgery, Neurology (clinical), Hereditary stroke, business, 030217 neurology & neurosurgery