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Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
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Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
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Sudden Onset of Involuntary Movement Disorders with Arteriovenous Malformations of the Basal Ganglia
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Idiopathic Hyperammonemia Associated with Cerebral arteriovenous Malformation
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Ocular Findings in the Sturge-Weber Syndrome
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Long-Term Outcome of 106 Consecutive Pediatric Ruptured Brain Arteriovenous Malformations After Combined Treatment
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MRI-Identified Pathology in Adults with New-Onset Seizures
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Clinical Reasoning: A Woman with Recurrent Aphasia and Visual Field Defects
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Antithrombotic Therapy and Bleeding Risk in a Prospective Cohort Study of Patients with Cerebral Cavernous Malformations
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Should Asymptomatic Patients with Hereditary Haemorrhagic Telangiectasia (HHT) be Screened for Cerebral Vascular Malformations? Data from 22 061 years of HHT Patient Life
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Risk of Endovascular Treatment of Brain Arteriovenous Malformations
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Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
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Recommendations for the Management of Intracranial Arteriovenous Malformations
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Intracerebral Haemorrhage in Young Adults: The Emerging Importance of Drug Misuse
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Intracerebral Haemorrhage Caused by Drug Abuse
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The Caput Medusae Sign
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Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
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Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
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