Criteria for the Diagnosis of Corticobasal Degeneration
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A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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A Middle-Aged Man with Progressive Gait Abnormalities
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An 82-year-old man with Worsening Gait
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
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Bilateral Basal Ganglia Lesions in Patients with End-Stage Diabetic Nephropathy
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Clinicopath Conf, Multiple-System Atrophy
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003
Progression of Parkinsonian Signs in Alzheimer's Disease
Neurol 54:1284-1289, Wilson,R.S.,et al, 2000
Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991
Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990
Neurological Findings in Alzheimer's Disease and Normal Aging
Arch Neurol 47:625-627, Glasko,D.,et al, 1990
Idiopathic Hypoparathyroidism with Extensive Brain Calcification & Persistent Neurologic Dysfunction
Neurol 37:307-309, Friedman,J.H.,et al, 1987
Clin. Path. Conference
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Neurologic Manifestations in Sarcoidosis
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Corticodentatonigral Degeneration with Neuronal Achromasia
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Huntington's Chorea
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