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Case Report - Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): A case report with review of literature, 01/2004
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is an inherited arterial disease, commonly overlooked or... 
ni04025 Autosomal dominant arteriopathy, Subcortical dementia, Notch 3 gene | Neurology
Journal
EMBO Molecular Medicine, ISSN 1757-4676, 06/2015, Volume 7, Issue 6, pp. 848 - 858
Journal Article
中华医学杂志:英文版, ISSN 0366-6999, 2017, Volume 130, Issue 9, pp. 1042 - 1048
Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditar5 small artery disease caused by... 
遗传性 | 视网膜血管 | 磁共振成像 | 光学相干层析成像 | 脑动脉 | 断层扫描 | Retinal vessels | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy | Magnetic resonance imaging | Optical coherence tomography | SMALL VESSEL DISEASE | MICROBLEEDS | HYPERINTENSITIES | ABNORMALITIES | MRI | Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy | Magnetic Resonance Imaging | MEDICINE, GENERAL & INTERNAL | CADASIL | Optical Coherence Tomography | Retinal Vessels | HIGH-RESOLUTION | NOTCH3 MUTATIONS | CHOROIDAL THICKNESS | CHINESE PATIENTS | Leukoencephalopathies - pathology | Retinal Vessels - metabolism | Humans | Middle Aged | Magnetic Resonance Imaging - methods | Male | Tomography, Optical Coherence - methods | Brain - metabolism | Adult | Female | Receptor, Notch3 - genetics | Mutation | Cerebral Infarction - pathology | Gene mutations | Analysis | Diagnostic imaging | Genetic aspects | Research | Leukoencephalopathy | Risk factors | Hypertension | Diabetic retinopathy | Nuclear magnetic resonance--NMR | Medical imaging | Migraine | Cognitive ability | Smooth muscle | Family medical history | Neurology | Hospitals | Diabetes | Age | Veins & arteries | Index Medicus | Original | Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy; Magnetic Resonance Imaging; Optical Coherence Tomography; Retinal Vessels
Journal Article
Stroke, ISSN 0039-2499, 01/2005, Volume 36, Issue 1, pp. 113 - 117
Background and Purpose - CADASIL is an inherited small-vessel disease responsible for lacunar strokes and cognitive impairment. The disease is caused by highly... 
Lacunar infarction | Mice, transgenic | CADASIL | Cognitive disorders | SUBCORTICAL INFARCTS | SIGNALING PATHWAYS | lacunar infarction | MYOGENIC RESPONSE | MICE LACKING | CLINICAL NEUROLOGY | LEUKOENCEPHALOPATHY | SMOOTH-MUSCLE | mice, transgenic | POSITRON-EMISSION-TOMOGRAPHY | CEREBRAL HEMODYNAMICS | PERIPHERAL VASCULAR DISEASE | AUTOSOMAL-DOMINANT ARTERIOPATHY | NOTCH3 MUTATIONS | cognitive disorders | Vasoconstrictor Agents - pharmacology | Vasoconstriction | Stress, Mechanical | CADASIL - physiopathology | Male | Mice, Transgenic | Proto-Oncogene Proteins - genetics | Arteries - drug effects | Pressure | Vasodilation | Mechanotransduction, Cellular | Receptors, Notch | Animals | Phenylephrine - pharmacology | Arteries - physiopathology | Receptor, Notch3 | Mice | CADASIL - etiology | Mutation | In Vitro Techniques | Receptor, Notch4 | Disease Models, Animal | Receptors, Cell Surface - genetics | Index Medicus | Phenylephrine/pharmacology | Proto-Oncogene Proteins/genetics | Life Sciences | Rec | Human health and pathology | Arteries/drug effects/physiopathology | CADASIL/etiology/physiopathology | Cardiology and cardiovascular system | Disease Models | Transgenic | Arteries | Receptors | genetics | Cell Surface | Phenylephrine | pharmacology | Proto-Oncogene Proteins | Notch | drug effects | Stress | etiology | physiopathology | Cellular | Vasoconstrictor Agents | Animal | Mechanical | Mechanotransduction
Journal Article
Frontiers in Neurology, 08/2019, Volume 10
Background and Purpose: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) mainly affects the cerebral small... 
7.0-Tesla magnetic resonance imaging (7.0-T MRI) | basal ganglia | cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) | time-of-flight-magnetic resonance angiography (TOF-MRA) | lenticulostriate arteries
Journal Article
Journal Article
Chinese Journal of Interventional Imaging and Therapy, ISSN 1672-8475, 10/2016, Volume 13, Issue 10, pp. 609 - 613
Journal Article
Annals of Indian Academy of Neurology, ISSN 0972-2327, 04/2016, Volume 19, Issue 2, pp. 272 - 274
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant angiopathy caused by a mutation... 
Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) | magnetic resonance imaging (MRI) | dementia | seizures | migraine | occipital lobe | CADASIL | PATTERNS | CLINICAL NEUROLOGY | Image in Neurology
Journal Article
Cureus, ISSN 2168-8184, 05/2018, Volume 10, Issue 5, p. e2631
The diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in adults can be challenging. Initially,... 
Stroke | Nuclear magnetic resonance--NMR | Medical imaging | Migraine | Cognitive ability | Headaches | Family medical history | Patients | Hospitals | Meningitis | Mutation | Rehabilitation | Dementia | Veins & arteries
Journal Article
International Journal of Clinical and Experimental Pathology, ISSN 1936-2625, 2015, Volume 8, Issue 2, pp. 1321 - 1327
Journal Article
Neurology and Clinical Neuroscience, ISSN 2049-4173, 01/2015, Volume 3, Issue 1, pp. 1 - 6
  Background Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, with an autosomal dominant mode of transmission, is an... 
NOTCH | cerebral small vessel disease | aggregates | cysteine | cerebral autosomal‐dominant arteriopathy with subcortical infarcts and leukoencephalopathy | Smooth muscle | Hypotheses | Mutation
Journal Article
Journal Article
Dementia and neurocognitive disorders, ISSN 1738-1495, 03/2016, Volume 15, Issue 1, pp. 15 - 19
Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most-common single gene disorder of cerebral small... 
phenotype | cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy | NOTCH3 | R544C mutation | Original | genotype
Journal Article
American Journal of Kidney Diseases, ISSN 0272-6386, 2008, Volume 52, Issue 2, pp. 340 - 345
Journal Article
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