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Ehlers-Danlos Syndromes
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The Tuberous Sclerosis Complex
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Sensorineural Hearing Loss in Children
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Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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Clinical and Genetic Aspects of Distal Myopathies
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
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Genetics of Cluster Headache Takes a Leap
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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
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Recurrent Cerebral Ischemia During Pregnancies
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Neuroradiologic Patterns and Novel Imaging Findings in Aicardi-Goutieres Syndrome
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Neurological Management of Von Hippel-Lindau Disease
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