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Cranial Cavernous Malformations
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Degenerative Diseases of the Nervous System, Olivopontocerebellar Atrophy
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Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
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Familial Dopa-Responsive Cervical Dystonia
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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Familial Dementia With Lewy Bodies
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Psychiatric Disturbances in Metachromatic Leukodystrophy
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Central Nervous System Lesions in von Hippel-Lindau Syndrome
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Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
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Cerebral Cavernous Malformations:Incidence and Familial Occurrence
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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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Familial Vascular Malformation or Chance Occurrence
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