Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
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Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
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Progressive Binasal Hemianopia
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Clinicopath Conf
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Orbital and Optic Pathway Sarcoidosis:MR Findings
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Multiple Sclerosis-Like Illness Occurring with Human Immunodeficiency Virus Infection
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Progressive Pontobulbar Palsy With Deafness
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Herpes Simplex & the Human Nervous System
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Failure of Vision in Childhood
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Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Neurosyphilis
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Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
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Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
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Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
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A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Mucolipidosis Type IV; Characteristic MRI Findings
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Neuro-Ophthalmic Manifestations of Lyme Disease
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Long-term Prognosis in Cerebral Venous Thrombosis:Follow-up of 77 Patients
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Neuro-Ophthalmologic Manifestations of Lyme Disease
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Acquired Ocular Visual Impairment in Children, 1960-1989
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Leber's Hereditary Optic Neuropathy, New Genetic Considerations
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Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992
Sarcoidosis of the Nervous System, A Clinical Approach
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
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Friedreich Ataxia
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MR Imaging of a Group I Case of Hallervorden-Spatz Disease
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Retinitis Pigmentosa
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Paraneoplastic Syndromes Involving the Eyes
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Neurosyphilis
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Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
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Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
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Familial Multisystem Atrophy with Possible Thalamic Dementia
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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Juvenile Metachromatic Leukodystrophy
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A Family with Hereditary Ataxia:HLA Typing
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Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
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Leber's Optic Neuropathy
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