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Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Outcome in Familial Subarachnoid Hemorrhage
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Hereditary Hemorrhagic Telangiectasia
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Intracranial Neoplasms and Paraneoplastic Disorders, Meningioma
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Clinical Manifestations and Diagnosis of Bicuspid Aortic Valve in Adults
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Screening Patients with a Family History of Subarachnoid Haemorrhage for Intracranial Aneurysms: Screening Uptake, Patient Characteristics and Outcome
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An unusual cause of stroke and hypoxia
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Aicardi-Gouti�res Syndrome
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Familial Cervical Artery Dissections: Clinical, Morphologic, and Genetic Studies
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Heritability of Carotid Artery Atherosclerotic Lesions
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Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
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Familial Leptomeningeal Amyloidosis With a Transthyretin Variant Asp18Gly Representing Repeated Subarachnoid Haemorrhages With Superficial Siderosis
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
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Repeated Screening for Intracranial Aneurysms in Familial Subarachnoid Hemorrhage
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Subarachnoid Hemorrhage
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Advances in the Genetics of Cerebrovascular Disease and Stroke
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Risk of Subarachnoid Haemorrhage in First Degree Relatives of Patients with Subarachnoid Haemorrhage: Follow Up Study Based on National Registries in Denmark
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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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Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
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Should We Screen for Familial Intracranial Aneurysm?
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Familial Subarachnoid Hemorrhage, Outcome Study
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Middle Cerebral Artery Main Stem Thrombosis in Two Siblings with Familial Thrombotic Thrombocytopenic Purpura
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