All Stories

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