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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Young Adult with Dysphagia and Severe Weight Loss
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
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A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
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Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
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Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
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Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
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Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
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A Middle-Aged Man with Progressive Gait Abnormalities
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"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
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Leg Weakness and Stiffness at the Emergency Room
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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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DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
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Cyclical Konzo Epidemics and Climate Variability
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Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
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The Hereditary Spastic Paraplegias
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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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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996
Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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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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Isolation of HTLV-II from Pt with Chronic, Prog Neurol Dis Clin Indistinguish from HAM/Tropical Spastic Paraparesis
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Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
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MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
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Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
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Chronic Neurodegenerative Disease Associated with HTLV-II Infection
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Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
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Intrathecal Baclofen for Severe Spinal Spasticity
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Treatment of Spastic Paresis
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Demyelinating Diseases
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Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988
Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987
Familial Multisystem Atrophy with Possible Thalamic Dementia
Neurol 34:1213-1217, Katz,D.A.,et al, 1984
Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980
Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy
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Jamaica Ginger Paralysis
Arch Neurol 35:530, Morgan,J.P.,et al, 1978
The Cervical Myelopathy Associated with Rheumatoid Arthritis:Analysis of 32 Patients, with Two Post-mortem Cases
Ann Neurol 3:144, Nakano,K.K.,et al, 1978
Adrenomyeloneuropathy:A Probable Variant of Adrenoleukodystrophy
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