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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
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Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
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A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024
A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023
Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
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An Intramedullary Mass
BMJ 374:m1948, Yang, J.S.,et al, 2021
A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021
Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020
"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019
Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019
Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019
Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019
Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018
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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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
Neurol 84:226-230,218, Wolf, N.I.,et al, 2015
Cyclical Konzo Epidemics and Climate Variability
Ann Neurol 77:371-380, Oluwole, O.S.A., 2015
Corticosteroid-Induced Paraplegia - A Diagnostic Clue for Spinal Dural Arterial Venous Fistula
JAMA Neurol 72:833-834, Hocker, S., 2015
A Case of Slowly Progressive Painful Paraparesis
Neurol 82:1476-1479, Corbetto, M.,et al, 2014
Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Tropical Spastic Paraparesis, HTLV-1 Infection
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Degenerative Diseases of the Nervous System, Familial Dementia with Spastic Paraparesis
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Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
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Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
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Longitudinally Extensive Transverse Myelitis in Neuro-Beh�et Disease
Neurol 80:e189-e190, Graham, D.,et al, 2013
Clinical Reasoning: A Case of Treatable Spastic Paraparesis
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Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
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Neurobrucellosis:Clinical and Neuroimaging Correlation
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Hereditary Spastic Paraplegia
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The Hereditary Spastic Paraplegias
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Prevalence and Clinical Features of HTLV Neurologic Disease in the HTLV Outcomes Study
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Recurrent Reversible Paraplegia
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Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
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Hereditary Spastic Paraparesis: A Review of New Developments
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Spastic Paraparesis after Anaesthesia
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Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
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Transdural Spinal Cord Herniation:Imaging and Clinical Spectra
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Granulomatous Compressive Thoracic Myelopathy as the Initial Manifestation of Wegener's Granulomatosis
Neurol 51:1769-1770, Kelly,P.J.,et al, 1998
HTLV-Associated Myelopathy in a Cohort of HTLV-I and HTLV-II Infected Blood Donors
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997
Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997
Progressive Deterioration of Intellect and Motor Function Occurring Several Decades after Cranial Irradiation
ARch Neurol 53:814-818, Duffey,P.,et al, 1996
Human T-Cell Lymphotropic Virus Type 1-Associated Myelopathy, Sjogren Syndrome, and Lymphocytic Pneumonitis
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
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