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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
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A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Neonatal Seizures
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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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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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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Decoding Cryptogenic Cardioembolism
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Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
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Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
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Metabolic Disease and Stroke: MELAS
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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New Players in the Genetics of Stroke
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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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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Impact of the Human Genome Projects and Identification of a Stroke Gene
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Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Stroke in Williams Syndrome
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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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Hereditary Hemorrhagic Telangiectasia
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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 Study of Twins and Stroke
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