Drug Resistant Epilepsy in a 61-Year-Old Man with Abnormal MRI Brain Findings and Management with Vagal Nerve Stimulator
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Updates on Sturge-Weber Syndrome
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Sturge-Weber Syndrome
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Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
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Sturge-Weber Syndrome
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Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
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Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
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Sturge-Weber Syndrome Presenting in a 58-Year-Old Woman With Seizures
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Outcomes of 32 Hemispherectomies for Sturge-Weber Worldwide
Neurol 59:1735-1738, Kossoff,E.H.,et al, 2002
Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
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Pulmonary Arteriovenous Malformations
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Sturge-Weber Syndrome
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Hereditary Hemorrhagic Telangiectasia
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Location of Port-Wine Stains and the Likelihood of Ophthalmic and/or CNS Complications
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Encephalotrigeminal Angiomatosis
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Epilepsy with Bilateral Occipital Calcifications:A Benign Onset with Progressive Severity
Neurol 38:913-920, Gobbi,G.,et al, 1988
Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987
Sturge-Weber-Dimitri Disease without Facial Nevus
Neurol 37:1063-1064, Taly,A.B.,et al, 1987
Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
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Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
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