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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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Red Papules on the Tongue of a Patient with Hemiparesis
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Hereditary Hemorrhagic Telangiectasia
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Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
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Cerebral Haemorrhagic Infarction in Young Patients with Hereditary Protein C Deficiency
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Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
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Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
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Neurological Management of Von Hippel-Lindau Disease
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Decoding Cryptogenic Cardioembolism
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Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
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Hypertrophic Cardiomyopathy A Systematic Review
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
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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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Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
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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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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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Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
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A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
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Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
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Hematologic Disorders and Ischemic Stroke
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Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
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Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
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Brain Abscess:Association with Pulmonary Arteriovenous Fistula and Hereditary Hemorrhagic Telangiectasia:3 Cases
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Renal Cell Carcinoma in von Hippel-Lindau Syndrome
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Familial Cavernous Malformations of the Central Nervous System & Retina
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Mendelian Etiologies of Stroke
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Livedo Reticularis & Cerebrovascular Lesions (Sneddon's Syndrome) , Clin, Radiolog & Path Features in Eight Cases
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Familial Stroke Syndrome Associated with Mitral Valve Prolapse
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Clinical pathological conference
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Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
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