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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
Stroke 32:877-882, Maher,C.O.,et al, 2001
Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
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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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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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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
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Analysis of Risk Factors for Stroke in a Cohort of Men Born in 1913
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MELAS Syndrome Involving a Mother & Two Children
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Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
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Abnormal Metabolism of y-Trace Alkaline Microprotein
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