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The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
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Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
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Conventional MRI and NOTCH3 Gene Screening in Sporadic CADASIL
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Migraine and Cerebral White Matter Lesions
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CADASIL: Cerebral Autosomal Subcortical Infarcts and Leukoecephalopathy
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Advances in the Genetics of Cerebrovascular Disease and Stroke
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
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CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
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The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
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Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Clinical Spectrum of CADASIL:A Study of 7 Families
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
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A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
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Cavernous Maliformations of the Central Nervous System
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Vascular Malformations of the Central Nervous System
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Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
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Complex Ataxia
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Recurrent Cerebral Ischemia During Pregnancies
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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A Teenager with Persistent Headache
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Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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Cranial Cavernous Malformations
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
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Neuromyelitis Optica Spectrum Disorders
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Red Papules on the Tongue of a Patient with Hemiparesis
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
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Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
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Degenerative Diseases of the Nervous System, Cerebellar Degeneration
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