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Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
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Progressive Supranuclear Palsy: A Current Review
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Whipples Disease
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Niemann-Pick Disease Type C: Two Cases and an Update
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Clinicopath Conf
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Creutzfeldt-Jakob Disease in a Young Woman
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Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996
Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996
Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993
Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
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Cortical-Basal Ganglionic Degeneration
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The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
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Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
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Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
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Adult Dystonic Lipidosis, Clin Histo & Biochem Findings of a Neurovisceral Storage Dis
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Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979
Whipple's Disease with Predominating Neuro-ophthalmic Manifestations
Ann Neurol 1:247-252, Finelli,P.F.,et al, 1977
Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Precipitous Deterioration of Motor Function, Cognition, and Behavior
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Criteria for the Diagnosis of Corticobasal Degeneration
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Central Nervous System Involvement in Whipple Disease
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Tau Forms in CSF as a Reliable Biomarker for Progressive Supranuclear Palsy
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Vascular Syndromes of the Thalamus
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002
Posterior Cerebral Artery Syndromes
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Parkinsonism-Recognition and Differential Diagnosis
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Mitochondrial DNA and Disease
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Progressive Supranuclear Palsy:Neuropathologic and Clinical Heterogeneity
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The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
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Fecal Incontinence
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Neurologic Manifestations of Giant Cell Arteritis
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Reversibility of CT and MR Findings in Neuro-Bechet Disease
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MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
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Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
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Subcortical Dementia
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Atypical Presentation of Progressive Supranuclear Palsy
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985
Neurosyphilis
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Mitochondrial Myopathies
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984
Correlation of Computed Tomographic, Angiographic, & Neuropathological Changes in Giant Cerebral Aneurysms
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Subcortical Dementia of Progressive Supranuclear Palsy
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Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974
Progressive Supranuclear Palsy:A Clinical, Pathological & Biochemical Study
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Cerebral Vascular Disease & Behavior
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