Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
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Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
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Epilepsy with Bilateral Occipital Calcifications:A Benign Onset with Progressive Severity
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Sturge-Weber-Dimitri Disease without Facial Nevus
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Medical Implications of Computed Tomography ("Cat scanning")
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