Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
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Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Neurofibromatosis Type I in Children
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Spinal Muscular Atrophy
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Pediatric Leigh Syndrome
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Neurodegeneration with Brain Iron Accumulation
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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Neurological Management of Von Hippel-Lindau Disease
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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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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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Somatic Mutations in Cerebral Cortical Malformations
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Sturge-Weber Syndrome
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Inherited Metabolic Diseases of the Nervous System, Galactosemia
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