Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
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Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
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Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
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Atypical Parkinsonian Syndromes: A General Neurologists Perspective
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
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A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015
Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Parkinsonism and Midbrain Syndromes with Hydrocephalus and Shunting
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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Degenerative Diseases of the Nervous System, Olivopontocerebellar Atrophy
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Parkin Disease
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The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
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Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
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Parkinsonism in HIV-Infected Patients on Highly Active Antiretroviral Therapy
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Progressive Supranuclear Palsy: A Current Review
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A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
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Practice Parameter: Diagnosis and Prognosis of New Onset Parkinson Disease (An Evidence-Based Review)
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Vascular Parkinsonism and Dementia in a CADASIL Case with Intact Nigrostriatal Dopaminergic System
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Dopamine-Responsive Dystonia
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The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
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Effect of Levodopa Treatment for Parkinsonism in Welders
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Clinicopath Conf, Multiple-System Atrophy
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Awakenings From Persistent Vegetative State: Report of Three Cases With Parkinsonism and Brain Stem Lesions on MRI
JNNP 74:1571-1573, Matsuda,W.,et al, 2003
HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
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Parkinsonism as the Presenting Manifestation of HIV Infection: Improvement on HAART
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Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
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Clinical Correlates of Vascular Parkinsonism
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Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
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Natural History & Survival of 14 Pts with Corticobasal Degeneration Confirmed as Postmortem Exam
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Early Dopaminergic Drug-Induced Hallucinations in Parkinsonian Patients
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Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
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Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
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Increased Incidence of Levodopa Therapy Following Metoclopramide Use
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Levodopa Failure in Chronic Manganism
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Extrapyramidal side Effects of Antiemetics Presenting as Psychiatric Illness
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Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
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Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989
Diffuse Lewy Body Disease:Clinical Features in 15 Cases
JNNP 52:709-717, Byrne,E.J., 1989
Chronic Manganese Intoxication
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Neuroleptic-Induced Parkinson's Syndrome:Clinical Features and Results of Treatment with Levodopa
JNNP 51:850-854, Hardie,R.J.&Lees,A.J., 1988
Movement Disorders & AIDS
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Classification of Parkinsonism
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Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
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Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
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Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
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