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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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Primary Brain Tumours in Adults
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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Intracranial Neoplasms and Paraneoplastic Disorders
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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The Tuberous Sclerosis Complex
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The Autosomal Recessive Cerebellar Ataxias
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Fragile X Premutation With Atypical Symptoms at Onset
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Mitochondrial DNA Polymerase-y and Human Disease
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Unusual Variants of Alexander's Disease
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Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child
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Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency
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Gliomatosis Cerebri: Molecular Pathology and Clinical Course
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Clinical and Genetic Aspects of Distal Myopathies
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New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
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Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
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The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
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The Inherited Ataxias and the New Genetics
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Hereditary Hemorrhagic Telangiectasia
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Clinical Genetics in Neurological Disease
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Myotonic Dystrophy with No Trinucleotide Repeat Expansion
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