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Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Cerebral Amyloid Angiopathy, A Critical Review
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Abnormal Metabolism of y-Trace Alkaline Microprotein
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Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
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RNF213 Polymorphisms in Intracranial Artery Dissection
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Alzheimers Disease
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Characyeristic features and progression of abnormalities on MRI for CARASIL
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Degenerative Diseases of the Nervous System, Alzheimer Disease
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
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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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Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
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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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Cerebrovascular Complications of Fabry's Disease
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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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A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
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Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
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Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
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Mendelian Etiologies of Stroke
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Gerstmann-Straussler-Scheinker Disease:Autopsy Study of a Familial Case
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Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
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A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023
Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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