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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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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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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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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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Hereditary Hemorrhagic Telangiectasia
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Protein S Deficiency in Middle-Aged Women with Stroke
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Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
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Clinicopath Conf
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations
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Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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Clinical Manifestations and Diagnosis of Bicuspid Aortic Valve in Adults
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Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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An unusual cause of stroke and hypoxia
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Aicardi-Gouti�res Syndrome
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Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
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Heritability of Carotid Artery Atherosclerotic Lesions
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Familial Leptomeningeal Amyloidosis With a Transthyretin Variant Asp18Gly Representing Repeated Subarachnoid Haemorrhages With Superficial Siderosis
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Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
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Recommendations for the Management of Patients with Unruptured Intracranial Aneurysms
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Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
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Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Recurrent Spontaneous Arterial Dissections-Risk in Familial Vs Nonfamilial Disease
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Familial Aorto-Cervicocephalic Arterial Dissections and Congenitally Bicuspid Aortic Valve
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Familial Occurrence of Neurocardiogenic Syncope
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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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A Clinical Study of Noonan Syndrome
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Familial Association of Intracranial Aneurysms and Cervical Artery Dissections
Stroke 22:1426-1430, Schievink,W.I.,et al, 1991
Risk of Brain Infarction in Familial Hypercholesterolemia
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Familial Cavernous Malformations of the Central Nervous System & Retina
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A Surgical Approach To The Treatment Of Fetal Hydrocephalus
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Placement Of Ventriculo-Amniotic Shunt For Hydrocephalus In A Fetus
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