المؤلفون: Jay Chol Choi

المصدر: Journal of Stroke
Journal of Stroke, Vol 17, Iss 1, Pp 7-16 (2015)

مصطلحات موضوعية: lcsh:Diseases of the circulatory (Cardiovascular) system, Candidate gene, Pathology, medicine.medical_specialty, Genome-wide association study, Cerebral small vessel diseases, CADASIL, Bioinformatics, Leukoencephalopathy, Autosomal dominant retinal vasculopathy with cerebral leukodystrophy, medicine, Stroke, Genetic association study, Intracerebral hemorrhage, Fabry disease, business.industry, Small Vessel Disease I, medicine.disease, Hyperintensity, lcsh:RC666-701, Special Review, Neurology (clinical), Cardiology and Cardiovascular Medicine, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::621c9609d4bf82e85db718d4cc915d9b
http://europepmc.org/articles/PMC4325630

المؤلفون: Jay Chol Choi

المصدر: Stroke Revisited: Diagnosis and Treatment of Ischemic Stroke ISBN: 9789811014239

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, business.industry, Genetic counseling, Homocystinuria, Disease, medicine.disease, Fabry disease, Leukoencephalopathy, Autosomal dominant retinal vasculopathy with cerebral leukodystrophy, medicine, cardiovascular diseases, CADASIL, business, Stroke

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9a4c4888aad5a25883dfcc50a9234570
https://doi.org/10.1007/978-981-10-1424-6_22

المؤلفون: Chiara Di Palma, Maria Teresa Dotti, Ilaria Taglia, Silvia Bianchi, Antonio Federico, Ilaria Di Donato

المصدر: Journal of the Neurological Sciences. 322:25-30

مصطلحات موضوعية: CARASIL, Collagen Type IV, Pathology, medicine.medical_specialty, Small vessels, CADASIL, Hereditary stroke, White matter, Leukoencephalopathy, Leukoencephalopathies, Autosomal dominant retinal vasculopathy with cerebral leukodystrophy, medicine, Humans, Vascular dementia, Receptor, Notch3, Stroke, Receptors, Notch, business.industry, Cerebral infarction, Serine Endopeptidases, Leukoencephalopathy, Progressive Multifocal, Alopecia, Cerebral Infarction, High-Temperature Requirement A Serine Peptidase 1, Phosphoproteins, medicine.disease, Magnetic Resonance Imaging, Fabry disease, Exodeoxyribonucleases, medicine.anatomical_structure, Neurology, Cerebral Small Vessel Diseases, Mutation, Fabry Disease, Spinal Diseases, Neurology (clinical), business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46c57ca67bf4a21334395f64630c1413
https://doi.org/10.1016/j.jns.2012.07.041

المؤلفون: Aaron M. Gruver, E. Rene Rodriguez, Lynn Schoenfield, Rula Hajj-Ali, Carmela D. Tan, Joshua F. Coleman

المصدر: Journal of Neuro-Ophthalmology. 31:20-24

مصطلحات موضوعية: Male, medicine.medical_specialty, Pathology, Central nervous system, Chromosome Disorders, Ophthalmic pathology, Frameshift mutation, chemistry.chemical_compound, Fatal Outcome, Autosomal dominant retinal vasculopathy with cerebral leukodystrophy, Ophthalmology, medicine, Humans, Treatment Failure, Genes, Dominant, Retinal Vasculitis, business.industry, Leukodystrophy, Retinal, Leukodystrophy, Metachromatic, Middle Aged, medicine.disease, medicine.anatomical_structure, chemistry, Disease Progression, Basal lamina, Histopathology, Neurology (clinical), business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d91663cb02d0e20cafd73dc3d5917f1
https://doi.org/10.1097/wno.0b013e3181f45dba

المؤلفون: Todd A. Hardy, Anna Richards, M. Kathryn Liszewski, Martin B. Delatycki, Martin Dichgans, Boukje de Vries, Arn M. J. M. van den Maagdenberg, J. A. Oosterhuis, Joost Haan, Mark Gilbert Grand, Hafsa Mamsa, Andreas Gschwendter, Mary J. van Schooneveld, Gisela M. Terwindt, Ruth Schäfer, Michael J. Kane, Kaate R J Vanmolkot, Paulus T. V. M. de Jong, John P. Atkinson, Suzanne Hodgkinson, Dirk Spitzer, Stanley F. Nelson, Anine H. Stam, Maria Louise Barilla-Labarca, Katya E. Kotschet, Rune R. Frants, Paula Bertram, Yumi Kasai, Michel D. Ferrari, Parul H. Kothari, Robert W. Baloh, David J. Kavanagh, Joanna C. Jen, Jijun Wan, Caroline W. Storimans, Michael D. McLellan, Rula A. Hajj-Ali

المساهمون: ANS - Amsterdam Neuroscience, Ophthalmology, Other departments

المصدر: Nature Genetics, 39(9), 1068-1070. Nature Publishing Group
Nature genetics, 39(9), 1068-1070. Nature Publishing Group

مصطلحات موضوعية: Exonuclease, Cytoplasm, NEPHROPATHY, Recombinant Fusion Proteins, Molecular Sequence Data, VASCULAR RETINOPATHY, DNA Exonuclease, HEREDITARY ENDOTHELIOPATHY, Transfection, Cell Line, Frameshift mutation, Degenerative disease, Retinal Diseases, AICARDI-GOUTIERES-SYNDROME, Autosomal dominant retinal vasculopathy with cerebral leukodystrophy, LOCUS, Genetics, medicine, Humans, Genetic Predisposition to Disease, Amino Acid Sequence, Genes, Dominant, Cell Nucleus, Brain Diseases, Microscopy, Confocal, Sequence Homology, Amino Acid, biology, Leukodystrophy, Phosphoproteins, medicine.disease, Molecular biology, Luminescent Proteins, Exodeoxyribonucleases, Mutation, biology.protein, Aicardi–Goutières syndrome, CEREBRORETINAL VASCULOPATHY, Cerebroretinal vasculopathy

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7304e32bdf45a345c07f7ac2dcfc7395
https://doi.org/10.1038/ng2082