Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021
Clinical Manifestations of the anti-IgLON5 Disease
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Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
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Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
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Progressive Supranuclear Palsy: A Current Review
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GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
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Wilson Disease
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Extrapyramidal Involvement in Rett's Syndrome
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A 6-Year-Old Girl with Progressive Toe Walking
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A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
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Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021
Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
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Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
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Functional Gait Disorders
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Orofacial Dyskinesia in a Young Man
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IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
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A Demure Teenager and Her Dystonic Foot
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A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
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Huntington Disease: Clinical Features and Diagnosis
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A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014
Degenerative Diseases of the Nervous System, Parkinson Disease
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The Limbic-Girdle Muscular Dystrophies
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Criteria for the Diagnosis of Corticobasal Degeneration
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Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
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Rapidly Progressive Corticobasal Degeneration Syndrome
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A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
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Dopamine-Responsive Dystonia
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
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Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998
Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998
Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997
Neurologic Aspects of Inflammatory Bowel Disease
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Clinicopath Conf
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Wilson's Disease:The Problem of Delayed Diagnosis
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Angelman Syndrome: Clinical Profile
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Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
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Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
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Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
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Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
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Neurotoxicity of Commonly Used Antineoplastic Agents
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Corticodentatonigral Degeneration with Neuronal Achromasia
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