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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Adverse Outcomes of Bacterial meningitis in School-Age Survivors
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Neurologic Aspects of Cobalamin Deficiency
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Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
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Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
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Demyelinating Diseases
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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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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Ears of the Lynx Magnetic Resonance Imaging Sign
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Degenerative Cervical Myelopathy
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Young Adult with Dysphagia and Severe Weight Loss
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
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Clinicopath Conf, Infantile Krabbe Disease
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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The Hereditary Spastic Paraplegias
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Subacute Combined Degeneration of the Spinal Cord
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Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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A Middle-aged Woman with Severe Scoliosis and Encephalopathy
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Leg Weakness and Stiffness at the Emergency Room
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Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
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Huntington Disease: Clinical Features and Diagnosis
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DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
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3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
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Intrathecal Baclofen Withdrawal Mimicking Sepsis
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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X-Linked Pure Familial Spastic Paraparesis
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Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
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Arginase Deficiency Presenting as Cerebral Palsy
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Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
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Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
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Bilateral Infarction of the Medullary Pyramids in Humans
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Intrathecal Baclofen for Severe Spinal Spasticity
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Treatment of Spastic Paresis
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987
Neurological Manifestations in Xeroderma Pigmentosum
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The Thyroid Gland:Its Relationship to Neurology
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Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
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