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Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
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The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
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Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
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Neonatal Seizures
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Spinal Muscular Atrophy
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Updates on Sturge-Weber Syndrome
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Congenital Cytomegalovirus Infection
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Telemedicine in Neurology
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Duchenne Muscular Dystrophy
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Accuracy of a Machine Learning Muscle MRI - Based Tool for the Diagnosis of Muscular Dystrophies
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Diagnostic Value of Cerebrospinal Fluid Neurofilament Light Protein in Neurology
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Congenital Myasthenic Syndromes in Adult Neurology Clinic
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Patient with Severe Moyamoya Disease Who Presents with Acute Cortical Blindness
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Clinicopathologic Conference, Paroxysmal Nocturnal Hemoglobinuria
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Clinicopathologic Conference, CAT Scratch Disease (Encephalopathy Associated with Bartonella Henselae)
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Recognizing Guillain-Barr� Syndrome in Preschool Children
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Muscle Histology vs MRI in Duchenne Muscular Dystrophy
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Late onset autism and anti-NMDA-receptor encephalitis
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Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Diagnosis and New Treatments in Muscular Dystrophies
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
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Cerebral Sinovenous Thrombosis in the Neonate
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Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
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The Tuberous Sclerosis Complex
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Mitochondrial DNA Polymerase-y and Human Disease
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Myotonic Dystrophy Type 2
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Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
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The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
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Polymyositis and Dermatomyositis
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A Novel, Blood-Based Diagnostic Assay for Limb Girdle Muscular Dystrophy 2B and Miyoshi Myopathy
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Diagnostic Criteria Used in Studies of Reflex Sympathetic Dystrophy
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New Strategy for Prenatal Diagnosis of X-Linked Disorders
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Practice Parameter: Screening and Diagnosis of Autism
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