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High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations
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Hereditary Hemorrhagic Telangiectasia
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Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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Familial Cavernous Malformations of the Central Nervous System & Retina
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Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
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Recurrent Cerebral Ischemia During Pregnancies
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Red Papules on the Tongue of a Patient with Hemiparesis
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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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Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
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Cavernous Maliformations of the Central Nervous System
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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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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Familial Versus Sporadic Cavernous Malformations: Differences in Developmental Venous Anomaly Association and Lesion Phenotype
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Familial Leptomeningeal Amyloidosis With a Transthyretin Variant Asp18Gly Representing Repeated Subarachnoid Haemorrhages With Superficial Siderosis
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Prospective Follow-up of 33 Asymptomatic Patients with Familial Cerebral Cavernous Malformations
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Familial Form of Intracranial Cavernous Angioma:MR Imaging Findings in 51 Families
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
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Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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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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Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
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Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
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Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
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Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
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Protein S Deficiency in Middle-Aged Women with Stroke
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Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
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Magnetic Resonance Imaging in a Family with Hereditary Cerebral Arteriovenous Malformations
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Cerebral Cavernous Malformations:Incidence and Familial Occurrence
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Familial Arteriovenous Malformation of the Brain
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Familial Arteriovenous Malformation
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