All Stories

  1. Eating Disorders and Parkinson’s Disease - 1: Comorbidities, Neurobiology and Family History
  2. Eating Disorders and Parkinson’s Disease - 2: Population Burden, Genetic Epidemiology and Shared Genomics
  3. CSF α-Synuclein Seed Amplification Assays and Alzheimer Disease Biomarkers in Dementia With Lewy Bodies
  4. Characteristics and mechanisms of cognitive impairment in Parkinson disease
  5. An Alternative Approach to the Finger‐Tapping Test in Parkinsonian Patients: Finger to Crease Instead of Finger to Tip
  6. Acute Pharmacodynamic Effects of Oral Levodopa on Blood Pressure in Parkinson's Disease
  7. Progressive Supranuclear Palsy—A Global Review
  8. Early Subtypes and Progressions of Progressive Supranuclear Palsy: A Data-Driven Brain Bank Study
  9. Differential memory enrichment of cytotoxic CD4 T cells in Parkinson’s disease patients reactive to α-synuclein
  10. T cell responses towards PINK1 and α-synuclein are elevated in prodromal Parkinson’s disease
  11. Association of CSF α-Synuclein Seeding Amplification Assay Results With Clinical Features of Possible and Probable Dementia With Lewy Bodies
  12. Why Crafting a Compelling Abstract Is Important to Summarize Research Findings
  13. Biosensor Strip for Rapid On‐site Assessment of Levodopa Pharmacokinetics along with Motor Performance in Parkinson's Disease
  14. Biosensor Strip for Rapid On‐site Assessment of Levodopa Pharmacokinetics along with Motor Performance in Parkinson's Disease
  15. PINK1 is a target of T cell responses in Parkinson’s disease
  16. Nicked tRNAs are stable reservoirs of tRNA halves in cells and biofluids
  17. CBD diagnostic criteria: exclusions as important as inclusions
  18. Digital Histological Study of Neocortical Grey and White Matter Tau Burden Across Tauopathies
  19. Author Correction: Safety and efficacy of anti-tau monoclonal antibody gosuranemab in progressive supranuclear palsy: a phase 2, randomized, placebo-controlled trial
  20. Nicked tRNAs are stable reservoirs of tRNA halves in cells and biofluids
  21. Sex Differences for Clinical Correlates of Alzheimer's Pathology in People with Lewy Body Pathology
  22. A Modified Progressive Supranuclear Palsy Rating Scale for Virtual Assessments
  23. Physician‐Assisted Dying: Access and Utilization in Patients with Movement Disorders
  24. Safety and efficacy of anti-tau monoclonal antibody gosuranemab in progressive supranuclear palsy: a phase 2, randomized, placebo-controlled trial
  25. The TOPAZ study: a home-based trial of zoledronic acid to prevent fractures in neurodegenerative parkinsonism
  26. Orthostatic hypotension preceding dementia with Lewy bodies by over 15 years: a clinicopathologic case report
  27. Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes?
  28. Hypertension and progressive supranuclear palsy
  29. Progression of two Progressive Supranuclear Palsy phenotypes with comparable initial disability
  30. End of life planning in parkinsonian diseases
  31. The virtual reality of Parkinson's disease freezing of gait: A systematic review
  32. Progress in the treatment of Parkinson-Plus syndromes
  33. Fall Prediction and Prevention Systems: Recent Trends, Challenges, and Future Research Directions
  34. Therapeutic options for Progressive Supranuclear Palsy including investigational drugs
  35. The Role of Stress as a Risk Factor for Progressive Supranuclear Palsy
  36. Which ante mortem clinical features predict progressive supranuclear palsy pathology?
  37. Radiological biomarkers for diagnosis in PSP: Where are we and where do we need to be?
  38. Psychometric Properties and Characteristics of the North-East Visual Hallucinations Interview in Parkinson's Disease
  39. Neuropsychiatric Predictors of Cognitive Decline in Parkinson Disease: A Longitudinal Study
  40. Understanding falls in progressive supranuclear palsy
  41. Progression of brain atrophy in PSP and CBS over 6 months and 1 year
  42. Minimal clinically important worsening on the progressive supranuclear Palsy Rating Scale
  43. Abolishing the 1-year rule: How much evidence will be enough?
  44. Environmental Exposures and Parkinson’s Disease
  45. Cognitive functioning in individuals with Parkinson’s disease and traumatic brain injury: A longitudinal study
  46. Clinical correlates of longitudinal brain atrophy in progressive supranuclear palsy
  47. Predicting disease progression in progressive supranuclear palsy in multicenter clinical trials
  48. Progression of Microstructural Degeneration in Progressive Supranuclear Palsy and Corticobasal Syndrome: A Longitudinal Diffusion Tensor Imaging Study
  49. Mild cognitive impairment in Parkinson's disease versus Alzheimer's disease
  50. α-synuclein genetic variability: A biomarker for dementia in Parkinson disease
  51. The new definition and diagnostic criteria of Parkinson's disease
  52. Technology in Parkinson's disease: Challenges and opportunities
  53. Power calculations and placebo effect for future clinical trials in progressive supranuclear palsy
  54. Relationship between uric acid levels and progressive supranuclear palsy
  55. Environmental and occupational risk factors for progressive supranuclear palsy: Case-control study
  56. Neuropsychiatric symptoms and their impact on quality of life in multiple system atrophy
  57. Progressive supranuclear palsy: progression and survival
  58. The first NINDS/NIBIB consensus meeting to define neuropathological criteria for the diagnosis of chronic traumatic encephalopathy
  59. Structural MRI Correlates of Episodic Memory Processes in Parkinson’s Disease Without Mild Cognitive Impairment
  60. Swallowing disturbances in the corticobasal syndrome
  61. Clinimetric Analysis of the Motor Section of the Progressive Supranuclear Palsy Rating Scale: Reliability and Factor Analysis
  62. Head injury exposure in PSP: a case-control study
  63. MDS clinical diagnostic criteria for Parkinson's disease
  64. MDS research criteria for prodromal Parkinson's disease
  65. The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease
  66. Development and validation of a carers quality-of-life questionnaire for parkinsonism (PQoL Carers)
  67. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy
  68. Scales to Assess Clinical Features of Progressive Supranuclear Palsy: MDS Task Force Report
  69. Cognitive performance and neuropsychiatric symptoms in early, untreated Parkinson's disease
  70. NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
  71. Pathophysiology, genetics, clinical features, diagnosis and therapeutic trials in progressive supranuclear palsy
  72. The Wearable Multimodal Monitoring System: A Platform to Study Falls and Near-Falls in the Real-World
  73. Correcting for Demographic Variables on the Modified Telephone Interview for Cognitive Status
  74. A disposable electrochemical biosensor for l-DOPA determination in undiluted human serum
  75. Serotonin Toxicity Association with Concomitant Antidepressants and Rasagiline Treatment: Retrospective Study (STACCATO)
  76. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
  77. Faculty Opinions recommendation of Low clinical diagnostic accuracy of early vs advanced Parkinson disease: clinicopathologic study.
  78. P3‐165: MILD COGNITIVE IMPAIRMENT AMONG PARKINSON'S DISEASE SUBJECTS IN THE UNIFORM DATA SET
  79. Davunetide in patients with progressive supranuclear palsy: a randomised, double-blind, placebo-controlled phase 2/3 trial
  80. Corticobasal Degeneration
  81. The utility of the Mattis Dementia Rating Scale in Parkinson's disease mild cognitive impairment
  82. Clinical and pathologic presentation in Parkinson's disease by apolipoprotein e4 allele status
  83. A Randomized Clinical Trial of High-Dosage Coenzyme Q10 in Early Parkinson Disease
  84. Cognition in movement disorders: Where can we hope to be in ten years?
  85. Time to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease
  86. Instrumental activities of daily living are impaired in Parkinson’s disease patients with mild cognitive impairment.
  87. Rate of decline in progressive supranuclear palsy
  88. A phase 2 trial of the GSK-3 inhibitor tideglusib in progressive supranuclear palsy
  89. Dissociation of Neural Mechanisms for Intersensory Timing Deficits in Parkinson’s Disease
  90. Pan-American Consortium of Multiple System Atrophy (PANMSA). A Pan-American multicentre cohort study of Multiple System Atrophy
  91. Parkinson's Disease Mild Cognitive Impairment: Application and Validation of the Criteria
  92. Behavioral abnormalities in progressive supranuclear palsy
  93. Faculty Opinions recommendation of Imaging of tau pathology in a tauopathy mouse model and in Alzheimer patients compared to normal controls.
  94. Primary Health Care Providers' Knowledge Gaps on Parkinson's Disease
  95. Predictors of performance-based measures of instrumental activities of daily living in nondemented patients with Parkinson’s disease
  96. Parkinsonian Syndromes
  97. Volumetric correlates of cognitive functioning in nondemented patients with Parkinson's disease
  98. Neuropsychiatric and cognitive disorders in other parkinsonian disorders
  99. Faculty Opinions recommendation of The natural history of multiple system atrophy: a prospective European cohort study.
  100. P4–096: APOE‐ɛ4 and clinical progression in Parkinson's disease
  101. The meaning of a “hippo” response on the Montreal Cognitive Assessment in Parkinson's disease
  102. Measuring mild cognitive impairment in patients with Parkinson's disease
  103. Criteria for the diagnosis of corticobasal degeneration
  104. Functional impairment in progressive supranuclear palsy
  105. White-Matter Changes Correlate with Cognitive Functioning in Parkinson’s Disease
  106. Long-duration Parkinson's disease: Role of lateralization of motor features
  107. Impact of Mild Cognitive Impairment on Health-Related Quality of Life in Parkinson's Disease
  108. The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer’s disease
  109. Toward magnetic resonance imaging biomarkers for progressive supranuclear palsy and multisystem atrophy
  110. Faculty Opinions recommendation of Pareidolias: complex visual illusions in dementia with Lewy bodies.
  111. Faculty Opinions recommendation of Parkinson subtypes progress differently in clinical course and imaging pattern.
  112. Executive Dysfunction Is the Primary Cognitive Impairment in Progressive Supranuclear Palsy
  113. Reply: Mild cognitive impairment in de novo Parkinson's disease according to Movement Disorder guidelines
  114. The pill questionnaire in a nondemented Parkinson's disease population
  115. Faculty Opinions recommendation of Clinical features of Parkinson disease when onset of diabetes came first: A case-control study.
  116. Pan-American Consortium of Multiple System Atrophy. Preliminary Report (P06.079)
  117. Polymorphic genes of detoxification and mitochondrial enzymes and risk for progressive supranuclear palsy: a case control study
  118. Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2
  119. Phosphorylated  -Synuclein in Parkinson's Disease
  120. Diagnostic criteria for mild cognitive impairment in Parkinson's disease: Movement Disorder Society Task Force guidelines
  121. Annonacin in Asimina triloba fruit: Implication for neurotoxicity
  122. Roles of Education and IQ in Cognitive Reserve in Parkinson’s Disease-Mild Cognitive Impairment
  123. Faculty Opinions recommendation of Quantitative EEG as a predictive biomarker for Parkinson disease dementia.
  124. Cytokine expression and microglial activation in progressive supranuclear palsy
  125. Faculty Opinions recommendation of α-Syn suppression reverses synaptic and memory defects in a mouse model of dementia with Lewy bodies.
  126. Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome
  127. Parkinsonism and Frontotemporal Dementia: The Clinical Overlap
  128. Progressive Supranuclear Palsy and Corticobasal Degeneration
  129. Brain-Lung-Thyroid Disease
  130. Copy Number Variation in Familial Parkinson Disease
  131. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
  132. MDS task force on mild cognitive impairment in Parkinson's disease: Critical review of PD‐MCI
  133. Faculty Opinions recommendation of Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
  134. Milestones in atypical and secondary Parkinsonisms
  135. Assessment of cognition in early dementia
  136. Woman with gait impairment and difficulty reading
  137. Faculty Opinions recommendation of Pramipexole for the treatment of depressive symptoms in patients with Parkinson's disease: a randomised, double-blind, placebo-controlled trial.
  138. A recommended scale for cognitive screening in clinical trials of Parkinson's disease
  139. Cognitive and neuropsychiatric effects of subthalamotomy for Parkinson’s disease
  140. Faculty Opinions recommendation of Levodopa, methylmalonic acid, and neuropathy in idiopathic Parkinson disease.
  141. A long-term study of istradefylline in subjects with fluctuating Parkinson's disease
  142. Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease
  143. A comparison of depression, anxiety, and health status in patients with progressive supranuclear palsy and multiple system atrophy
  144. Faculty Opinions recommendation of Lentiviral overexpression of GRK6 alleviates L-dopa-induced dyskinesia in experimental Parkinson's disease.
  145. H1/H1 genotype influences symptom severity in corticobasal syndrome
  146. Faculty Opinions recommendation of Increased melanoma risk in Parkinson disease: a prospective clinicopathological study.
  147. Bradykinesia
  148. Tauopathies
  149. Initial clinical manifestations of Parkinson's disease: features and pathophysiological mechanisms
  150. Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria
  151. Incidence of and risk factors for cognitive impairment in an early Parkinson disease clinical trial cohort
  152. Genomewide association study for onset age in Parkinson disease
  153. Faculty Opinions recommendation of Neural transplants in patients with Huntington's disease undergo disease-like neuronal degeneration.
  154. Faculty Opinions recommendation of Cerebellar involvement in progressive supranuclear palsy: A clinicopathological study.
  155. Faculty Opinions recommendation of A controlled trial of antidepressants in patients with Parkinson disease and depression.
  156. Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options
  157. Review article Progressive supranuclear palsy revisited
  158. Reply: Corticobasal syndrome with Alzheimer's disease pathology
  159. Parkinson’s Disease: An Overview of Pathogenesis
  160. Is it PD, PSP, CBD, DLB, or MSA?
  161. Faculty Opinions recommendation of Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy.
  162. Genomewide association study for susceptibility genes contributing to familial Parkinson disease
  163. The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study
  164. Faculty Opinions recommendation of Cerebral cortex and the clinical expression of Huntington's disease: complexity and heterogeneity.
  165. Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: The GenePD study
  166. Replication of association between ELAVL4 and Parkinson disease: the GenePD study
  167. Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study
  168. Faculty Opinions recommendation of Vestibular, saccadic and fixation abnormalities in genetically confirmed Friedreich ataxia.
  169. Progressive supranuclear palsy and corticobasal degeneration: similarities and differences
  170. Adenosine A2Areceptor antagonist istradefylline (KW-6002) reduces “off” time in Parkinson's disease: A double-blind, randomized, multicenter clinical trial (6002-US-005)
  171. Preface
  172. Current and future therapeutic approaches in progressive supranuclear palsy
  173. Biology and Neuropathology of Dementia in Syphilis and Lyme Disease
  174. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
  175. Clinical and Therapeutic Aspects of Dementia in Syphilis and Lyme Disease
  176. Clinical aspects and biology of normal pressure hydrocephalus
  177. Clinical aspects of Parkinson dementia
  178. Clinical symptoms in Alzheimer's disease
  179. History of Dementia
  180. Mild cognitive impairment
  181. Neuropathology and genetics of corticobasal degeneration
  182. Neuropathology of Pick body disease
  183. Neuropathology of Hereditary Forms of Frontotemporal Dementia and Parkinsonism
  184. Perspectives of Alzheimer's disease treatments
  185. Quality of Life in Dementias
  186. The Epidemiology of vascular dementia
  187. The Neuropathology of Vascular and Mixed Dementia and Vascular Cognitive Impairment
  188. Diagnostic procedures for Parkinson's disease dementia: Recommendations from the movement disorder society task force
  189. Update of atypical parkinsonian disorders
  190. Clinical diagnostic criteria for dementia associated with Parkinson's disease
  191. The Etiopathogenesis of Parkinson Disease and Suggestions for Future Research. Part II
  192. The Etiopathogenesis of Parkinson Disease and Suggestions for Future Research. Part I
  193. Identification of a Novel Risk Locus for Progressive Supranuclear Palsy by a Pooled Genomewide Scan of 500,288 Single-Nucleotide Polymorphisms
  194. Faculty Opinions recommendation of Neurosurgery at an earlier stage of Parkinson disease: a randomized, controlled trial.
  195. Faculty Opinions recommendation of Randomized, blind, controlled trial of transdermal rotigotine in early Parkinson disease.
  196. Neurobiology of Progressive Supranuclear Palsy
  197. Unraveling progressive supranuclear palsy: from the bedsideback to the bench
  198. Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: The GenePD Study
  199. Alzheimer's disease presenting as corticobasal syndrome
  200. Measuring quality of life in PSP
  201. Faculty Opinions recommendation of Compulsive drug use linked to sensitized ventral striatal dopamine transmission.
  202. Atypical Parkinsonian Disorders--Clinical and Research Aspects * Edited by Irene Litvan * Human Press, 2005. ISBN 1-588-29-331-9. $175.00
  203. Influence of Heterozygosity for Parkin Mutation on Onset Age in Familial Parkinson Disease
  204. Current and future treatments in progressive supranuclear palsy
  205. Penguins and hummingbirds: Midbrain atrophy in progressive supranuclear palsy
  206. Faculty Opinions recommendation of Substantia nigra tangles are related to gait impairment in older persons.
  207. Faculty Opinions recommendation of A randomized, double-blind, futility clinical trial of creatine and minocycline in early Parkinson disease.
  208. Book Review Drug Induced Movement Disorders Second edition. Edited by Stewart A. Factor, Anthony E. Lang, and William J. Weiner. 466 pp. Malden, Mass., Blackwell Futura, 2005. $120. 1-4051-2619-1
  209. Lrrk2 and Lewy body disease
  210. Midbrain atrophy in progressive supranuclear palsy: comparison of two dimensional planimetric- with three dimensional volumetric measurements
  211. BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study
  212. Diagnosis and management of dementia with Lewy bodies: Third report of the DLB consortium
  213. High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy
  214. Cognitive and behavioral aspects of PSP since Steele, Richardson and Olszewski’s description of PSP 40 years ago and Albert’s delineation of the subcortical dementia 30 years ago
  215. “Applause sign” helps to discriminate PSP from FTD and PD
  216. Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome
  217. Bilateral subthalamotomy in Parkinson's disease: initial and long-term response
  218. Atypical Parkinsonian Disorders
  219. What is an Atypical Parkinsonian Disorder?
  220. Progressive Supranuclear Palsy
  221. Progressive Supranuclear Palsy and Corticobasal Degeneration
  222. Update on progressive supranuclear palsy
  223. ATYPICAL PARKINSONIAN DISORDERS
  224. Diagnostic issues in non-AD dementias
  225. Magnetic resonance imaging-based volumetry differentiates progressive supranuclear palsy from corticobasal degeneration
  226. Verifying Clinical Criteria for Parkinsonian Disorders with CART Decision Trees
  227. Correlation of dopamine transporter imaging with parkinsonian motor handicap: How close is it?
  228. Update on epidemiological aspects of progressive supranuclear palsy
  229. Performance on the dementia rating scale in Parkinson's disease with dementia and dementia with Lewy bodies: comparison with progressive supranuclear palsy and Alzheimer's disease
  230. SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders
  231. Progression of gait, speech and swallowing deficits in progressive supranuclear palsy
  232. Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia
  233. Yes/no reversals as neurobehavioral sequela: a disorder of language, praxis, or inhibitory control?
  234. Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration
  235. Freezing of gait in postmortem‐confirmed atypical parkinsonism
  236. Mitochondrial Dysfunction in Cybrid Lines Expressing Mitochondrial Genes from Patients with Progressive Supranuclear Palsy
  237. Corticobasal Degeneration and Related Disorders
  238. Effects of closed traumatic brain injury and genetic factors on the development of Alzheimer's disease
  239. Neuropsychiatric assessment of Gilles de la Tourette patients: Comparative study with other hyperkinetic and hypokinetic movement disorders
  240. Randomized placebo-controlled trial of donepezil in patients with progressive supranuclear palsy
  241. Traumatic brain injury as a risk factor for Alzheimer disease. Comparison of two retrospective autopsy cohorts with evaluation of ApoE genotype
  242. Tau genotype: No effect on onset, symptom severity, or survival in progressive supranuclear palsy
  243. Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
  244. Therapy and management of frontal lobe dementia patients
  245. Comparison of apraxia in corticobasal degeneration and progressive supranuclear palsy
  246. An open letter to the Committee on The Nobel Prize in Medicine
  247. Impairment of eyeblink classical conditioning in progressive supranuclear palsy
  248. Progression of Dysarthria and Dysphagia in Postmortem-Confirmed Parkinsonian Disorders
  249. Neuropsychiatric Symptoms of Patients With Progressive Supranuclear Palsy and Parkinson's Disease
  250. Neuropsychiatric Symptoms of Patients With Progressive Supranuclear Palsy and Parkinson's Disease
  251. Diagnosis and Management of Progressive Supranuclear Palsy
  252. The FAB
  253. Progression of Hoehn and Yahr stages in parkinsonian disorders: A clinicopathologic study
  254. Research goals in progressive supranuclear palsy
  255. Scientific position paper of the Movement Disorder Society evaluation of surgery for Parkinson's disease
  256. Longitudinal ocular motor study in corticobasal degeneration and progressive supranuclear palsy
  257. Language disturbances in corticobasal degeneration
  258. Pupillary diameter assessment: Need for a graded scale
  259. Frontal Assessment Battery
  260. Importance of deficits in executive functions
  261. Evaluation of surgery for Parkinson’s disease
  262. Progression of falls in postmortem-confirmed Parkinsonian disorders
  263. Time course of symptomatic orthostatic hypotension and urinary incontinence in patients with postmortem confirmed parkinsonian syndromes: a clinicopathological study
  264. Atypical parkinsonism in the French West Indies
  265. Accuracy of four clinical diagnostic criteria for the diagnosis of neurodegenerative dementias
  266. Recent advances in atypical parkinsonian disorders
  267. Effects of Physostigmine on Swallowing and Oral Motor Functions in Patients with Progressive Supranuclear Palsy: A Pilot Study
  268. Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear Palsy
  269. Clinicopathologic Case Report
  270. Consensus statement on the diagnosis of multiple system atrophy
  271. Ideomotor apraxia in progressive supranuclear palsy: A case study
  272. Ideomotor apraxia in progressive supranuclear palsy: A case study
  273. A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration
  274. Consensus statement on the diagnosis of multiple system atrophy
  275. Parkinsonian Features
  276. Caregiving in progressive supranuclear palsy
  277. Neuropsychiatric features of corticobasal degeneration
  278. Neuropsychiatric Assessment of Patients With Hyperkinetic and Hypokinetic Movement Disorders
  279. Accuracy of the clinical diagnosis of postencephalitic parkinsonism: a clinicopathologic study
  280. Reliability of the NINDS Myotatic Reflex Scale
  281. Pharmacological Therapy in Progressive Supranuclear Palsy
  282. Is EEG useful in the differential diagnosis of parkinsonism?
  283. Apathy Is Not Depression
  284. Dysfunction of Ib (Autogenic) spinal inhibition in patients with progressive supranuclear palsy
  285. Clinical and Genetic Aspects of Progressive Supranuclear Palsy
  286. Accuracy of the Clinical Diagnoses of Lewy Body Disease, Parkinson Disease, and Dementia With Lewy Bodies
  287. Progressive supranuclear palsy
  288. Retrospective application of a set of clinical diagnostic criteria for the diagnosis of multiple system atrophy
  289. Apolipoprotein Eepsilon4 (Epsilon) Allele Does Not Affect the Onset or Symptom Severity in Progressive Supranuclear Palsy
  290. What are the Obstacles for an Accurate Clinical Diagnosis of Pick's disease?
  291. Methodological and Research Issues in the Evaluation of Biological Diagnostic Markers for Alzheimer’s Disease
  292. Consensus Report of the Working Group on: “Molecular and Biochemical Markers of Alzheimer’s Disease” 11The names of the Working Group Members and the names of the Working Group Advisory Committee Members are listed in the Appendix A(section VI). 22The ...
  293. Natural history and survival of 14 patients with corticobasal degeneration confirmed at postmortem examination
  294. PROGRESSIVE SUPRANUCLEAR PALSY
  295. Limb shaking in multiple system atrophy
  296. Progressive supranuclear gaze palsy is in linkage disequilibrium with theτ and not the α-synuclein gene
  297. Proton magnetic resonance spectroscopic imaging in progressive supranuclear palsy, Parkinson's disease and corticobasal degeneration
  298. What Is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy?
  299. The clinical and pathologic hallmarks of progressive supranuclear palsy
  300. Supranuclear gaze palsy and eyelid apraxia in postencephalitic parkinsonism
  301. What are the obstacles for an accurate clinical diagnosis of Pick's disease? A clinicopathologic study
  302. Characterizing swallowing abnormalities in progressive supranuclear palsy
  303. Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study
  304. Accuracy of the Clinical Diagnosis of Corticobasal Degeneration: A Clinicopathologic Study
  305. REPLY FROM THE AUTHORS
  306. A Reappraisal of Reliability and Validity Studies in Stroke
  307. Neuropsychiatric aspects of progressive supranuclear palsy
  308. Can tropicamide eye drop response differentiate patients with progressive supranuclear palsy and Alzheimer's disease from healthy control subjects?
  309. Reliability of the NINDS Myotatic Reflex Scale
  310. Preserved cognitive processes in cerebellar degeneration
  311. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): Report of the NINDS-SPSP International Workshop
  312. Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study.
  313. Visualizing Cortical Activation during Mental Calculation with Functional MRI
  314. Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome)
  315. Progressive supranuclear palsy: a clinicopathological study of 21 cases
  316. 641 Accuracy of the clinical diagnosis of pick's disease
  317. Validity and Reliability of the Preliminary NINDS Neuropathologic Criteria for Progressive Supranuclear Palsy and Related Disorders
  318. What can artificial neural networks teach us about neurodegenerative disorders with extrapyramidal features?
  319. Neuropsychological Features of Progressive Supranuclear Palsy
  320. What can preservation of autobiographic memory after muscarinic blockade tell us about the scopolamine model of dementia?
  321. Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)
  322. Pharmacological evaluation of the cholinergic system in progressive supranuclear palsy
  323. Cognitive disturbances in progressive supranuclear palsy
  324. Cholinergic approaches to the treatment of progressive supranuclear palsy
  325. Cerebellar cognition
  326. Cognitive planning deficit in patients with cerebellar atrophy
  327. CSF galanin and neuropeptide Y immunoreactivity in progressive supranuclear palsy
  328. Cerebrospinal fluid acetylcholinesterase in progressive supranuclear palsy: reduced activity relative to normal subjects and lack of inhibition by oral physostigmine.
  329. Progressive supranuclear palsy
  330. Differential memory and executive functions in demented patients with Parkinson's and Alzheimer's disease.
  331. Effects of Physostigmine on Spatial Attention in Patients With Progressive Supranuclear Palsy
  332. Selective Deficits in Alzheimer and Parkinsonian Dementia: Visuospatial Function
  333. Selective deficits in cognition and memory in high-functioning parkinsonian patients.
  334. Frontal Lobe Function in Progressive Supranuclear Palsy
  335. Implicit Learning in Patients with Alzheimer's Disease
  336. Physostigmine treatment of progressive supranuclear palsy
  337. Memory Impairment in Patients With Progressive Supranuclear Palsy
  338. Multiple Memory Deficits in Patients With Multiple Sclerosis
  339. Slowed Information Processing in Multiple Sclerosis
  340. Unilateral left cerebral deterioration documented by CT, MRI, and neuropsychological studies: A possible case of pick's disease
  341. Behcet's syndrome masquerading as tumor
  342. Does reversed laterality really exist in dextrals? A case study
  343. Agitation and Apathy in Hyper- and Hypokinetic Movement Disorders
  344. Measuring quality of life in progressive supranuclear palsy
  345. Management of cognitive impairment in Parkinson's disease
  346. Faculty of 1000 evaluation for Associations between Anticholinergic Burden and Adverse Health Outcomes in Parkinson Disease.
  347. Case Studies