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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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Pediatric Leigh Syndrome
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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The Autosomal Recessive Cerebellar Ataxias
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Detection of Human Herpesvirus-6 in Cerebrospinal Fluid of Patients with Encephalitis
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Neurofibromatosis Type 2
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Hereditary Hemorrhagic Telangiectasia
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Muscular Dystrophies
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Zika Virus Associated with Microcephaly
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Clinicopathologic Conference, Oligdendroglioma II/IV with IDH1 R132H mutation and codelation of 1p and 19q
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Spinal Muscular Atrophy A Timely Review
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A 23-Year-Old Man With Seizures and Visual Deficit
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CSF Evaluation in Primary CNS Lymphoma Patients by PCR of the CDR III IgH Genes
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Alzheimer Disease
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Hereditary Recurrent Focal Neuropathies, Clinical and Molecular Features
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Molecular Basis of the Neurodegenerative Disorders
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PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
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Trinucleotide Repeat Expansion in Neurological Disease
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Leber's Hereditary Optic Neuropathy, New Genetic Considerations
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Molecular Genetics in Neurology
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