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Neurofibromatosis Type 2
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Gliomatosis Cerebri: Molecular Pathology and Clinical Course
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Mitochondrial DNA and Disease
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Pediatric Leigh Syndrome
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Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing
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The Autosomal Recessive Cerebellar Ataxias
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Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008
CSF Evaluation in Primary CNS Lymphoma Patients by PCR of the CDR III IgH Genes
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Hereditary Hemorrhagic Telangiectasia
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Molecular Genetics in Neurology
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Muscular Dystrophies
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Clinicopathologic Conference, Oligdendroglioma II/IV with IDH1 R132H mutation and codelation of 1p and 19q
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Intracranial Neoplasms and Paraneoplastic Disorders
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Spinal Muscular Atrophy A Timely Review
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Detection of Human Herpesvirus-6 in Cerebrospinal Fluid of Patients with Encephalitis
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Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007
The Tuberous Sclerosis Complex
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Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
Lancet 361:1552-1554, Reynolds,R.M., et al, 2003
von Hippel-Lindau Disease
Lancet 361:2059-2067, Lonser,R.R.,et al, 2003
Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
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Molecular Basis of the Neurodegenerative Disorders
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von Hippel-Lindau Disease
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Investigation of Muscle Disease
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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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Trinucleotide Repeat Expansion in Neurological Disease
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Gene Therapy for Neurologic Disease
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