Online citations, reference lists, and bibliographies.
← Back to Search

Comparison Of Motor, Cognitive, And Behavioral Features In Progressive Supranuclear Palsy And Parkinson's Disease

N. Cordato, G. Halliday, D. Caine, J. Morris
Published 2006 · Psychology, Medicine

Save to my Library
Download PDF
Analyze on Scholarcy
Share
Major clinical features and global measures were systematically evaluated and compared in progressive supranuclear palsy (PSP) and Parkinson's disease (PD). In addition to gaze palsy and early postural instability in PSP, absence of levodopa‐induced dyskinesia, frontalis muscle overactivity, primitive reflexes, visuospatial impairment, and substantial frontal behavioral disturbances differentiated almost all patients with this disorder from PD. For PSP, behavioral changes related to severity of general disability, thereby challenging previous models of relationships between behavior, motor, and cognitive disturbance for this disorder. © 2005 Movement Disorder Society
This paper references
10.1093/brain/125.4.789
Frontal atrophy correlates with behavioural changes in progressive supranuclear palsy.
N. Cordato (2002)
10.1001/ARCHNEUR.55.3.372
Cognitive dysfunction and impaired organization of complex motility in degenerative parkinsonian syndromes.
D. Monza (1998)
10.1093/BRAIN/114.3.1457
Language functions in progressive supranuclear palsy.
K. Podoll (1991)
10.1007/BF00878659
Neuropsychological performance, disease severity, and depression in progressive supranuclear palsy
T. Esmonde (2004)
10.1212/WNL.53.6.1292
Accuracy of four clinical diagnostic criteria for the diagnosis of neurodegenerative dementias
O. Lopez (1999)
10.1002/MDS.870040402
Eyelid movement abnormalities in progressive supranuclear palsy
Lawrence I. Golbe (1989)
10.1016/0002-9394(72)90740-4
Ocular manifestations in progressive supranuclear palsy.
D. Pfaffenbach (1972)
10.1093/BRAIN/120.1.65
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
I. Litvan (1997)
10.1016/0022-3956(82)90033-4
Development and validation of a geriatric depression screening scale: a preliminary report.
J. Yesavage (1982)
10.1017/cbo9780511763281.013
[The Unified Parkinson's Disease Rating Scale].
A. Bonnet (2000)
10.1212/WNL.44.7.1264
Are explicit memory disorders of progressive supranuclear palsy related to damage to striatofrontal circuits? Comparison with Alzheimer's, Parkinson's, and Huntington's diseases
B. Pillon (1994)
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-RichardsonOlszewski Syndrome): report of the NINDS-SPSP International Workshop
I Litvan (1996)
10.1136/jnnp.64.3.320
Spontaneous and reflex activity of facial muscles in dystonia, Parkinson’s disease, and in normal subjects
G. Deuschl (1998)
10.1212/01.WNL.0000052686.97625.27
Progression of gait, speech and swallowing deficits in progressive supranuclear palsy
C. Götz (2003)
10.1007/s004010050446
Progressive supranuclear palsy: a clinicopathological study of 21 cases
M. Verny (1996)
10.1002/1531-8249(200006)47:6<718::AID-ANA4>3.0.CO;2-J
Regional brain atrophy in progressive supranuclear palsy and Lewy body disease
N. Cordato (2000)
10.1016/0022-3956(75)90026-6
"Mini-mental state". A practical method for grading the cognitive state of patients for the clinician.
M. Folstein (1975)
10.1212/WNL.47.5.1184
Neuropsychiatric aspects of progressive supranuclear palsy
I. Litvan (1996)
Recent Developments in Parkinson's Disease
S. Fahn (1986)
10.1002/MDS.870120310
Comparison of swallowing function in Parkinson's disease and progressive supranuclear palsy
B. Johnston (1997)
Which clinical features differentiate progressive supranuclear palsy (Steele- RichardsonOlszewski syndrome) from related disorders? A clinicopathological study. Brain 1997;120:65–74
I Litvan (1997)
10.1212/WNL.47.1.1
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome)
I. Litvan (1996)
10.1136/jnnp.46.2.162
Comparison of three primitive reflexes in neurological patients and in normal individuals.
J. P. Jensen (1983)
Neuropsychological assessment, 3rd ed.
M. Lezak (1995)
10.1017/S0317167100021053
Frontal behavioral inventory: diagnostic criteria for frontal lobe dementia.
A. Kertesz (1997)
10.1136/jnnp.58.2.167
Progressive supranuclear palsy: neuropathologically based diagnostic clinical criteria.
S. Collins (1995)
Dementia: the estimation of pre-morbid intelligence levels using the New Adult Reading Test. Cortex 1978;14:234–244
HE Nelson (1978)
10.1006/BRCG.1995.1260
Neuropsychological Features of Progressive Supranuclear Palsy
J. Grafman (1995)
10.1212/WNL.34.5.677
Blink rates and disorders of movement
C. Karson (1984)
10.1097/00001756-199510010-00032
Micrographia in Parkinson's disease.
J. L. Contreras-Vidal (1995)
10.1136/jnnp.69.3.313
Neuropsychological follow up in patients with Parkinson's disease, striatonigral degeneration-type multisystem atrophy, and progressive supranuclear palsy
P. Soliveri (2000)
10.1002/mds.10234
Freezing of gait in postmortem‐confirmed atypical parkinsonism
J. Müller (2002)
10.1159/000113224
Innervation of propatagial musculature in a flying squirrel, Glaucomys volans (Rodentia, Sciuridae).
Chickering Jg (1996)
Members of the UPDRS Development Committee. Unified Parkinson's Disease Rating Scale
S. Fahn (1987)
10.1016/S0010-9452(78)80049-5
Dementia: The Estimation of Premorbid Intelligence Levels Using the New Adult Reading Test
H. Nelson (1978)
10.1001/ARCHNEUR.58.2.259
Progression of dysarthria and dysphagia in postmortem-confirmed parkinsonian disorders.
J. Müller (2001)
10.1136/jnnp.60.6.615
Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study.
I. Litvan (1996)
10.1007/s00415-007-2004-7
Neuropsychological assessment
W. Sturm (2007)



This paper is referenced by
Dysphagia and Dysarthria: The Relationship of Sensorimotor- Speech and Swallowing
D. Trahan (2016)
10.1002/9781444344110.CH13
13. Executive Functioning
R. Stern (2011)
10.1007/978-1-4614-3106-0_22
Movement Disorders with Dementia in Older Adults
A. Tröster (2013)
10.1111/jnp.12053
Frontal deficits differentiate progressive supranuclear palsy from Parkinson's disease.
Y. Lee (2016)
10.1016/j.jns.2013.01.034
The interrelationship between non-motor symptoms in Atypical Parkinsonism
Chan-Nyoung Lee (2013)
10.1002/acn3.195
The cognitive profile of prion disease: a prospective clinical and imaging study
D. Caine (2015)
10.1201/B11703-19
Aging and Handwriting
Michael P. Caligiuri (2012)
10.1176/appi.neuropsych.17010012
Use of the Neuropsychiatric Inventory to Characterize the Course of Neuropsychiatric Symptoms in Progressive Supranuclear Palsy.
M. Jecmenica-Lukic (2018)
10.1007/978-3-319-09537-0_7
Neuropsychiatric Manifestations in Atypical Parkinsonian Syndromes
Iva Stankovic (2015)
10.1007/s00702-016-1589-3
Montreal Cognitive Assessment (MoCA) and Mini-Mental State Examination (MMSE) performance in progressive supranuclear palsy and multiple system atrophy
E. Fiorenzato (2016)
10.1002/mds.23059
The grasp reflex: A symptom in need of treatment
T. Mestre (2010)
10.1007/s00415-019-09463-1
Language impairment in progressive supranuclear palsy and corticobasal syndrome
Katie A Peterson (2019)
Progressive Supranuclear Palsy: New Diagnostic and Therapeutic Strategies
D G Lichter (2018)
Reports Real-time Visualization of Altered Gastric Motility by Magnetic Resonance Imaging in Patients with Parkinson ’ s Disease
Marcus Michael Unger (2010)
10.1002/mds.22841
Real‐time visualization of altered gastric motility by magnetic resonance imaging in patients with Parkinson's disease
M. Unger (2010)
10.1007/s00415-018-9038-x
Comparative cognitive and neuropsychiatric profiles between Parkinson’s disease, multiple system atrophy and progressive supranuclear palsy
G. Santangelo (2018)
10.1002/mds.23060
Endoscopic characteristics and levodopa responsiveness of swallowing function in progressive supranuclear palsy
T. Warnecke (2010)
Comparison of Cognitive, Affective, and Activities of Daily Living Functions inPatients with Parkinsonâs Disease and Progressive Supranuclear Palsy
Koji Abe (2019)
10.1017/S1041610209008862
Pattern of behavioral disturbances in corticobasal degeneration syndrome and progressive supranuclear palsy.
B. Borroni (2009)
Myasthenia Gravis mimics: An audit of cases identified at Groote Schuur Hospital over 20 years
Saara Ndinelago Neshuku (2019)
10.3233/JAD-170743
Aphasia in Progressive Supranuclear Palsy: As Severe as Progressive Non-Fluent Aphasia.
J. Burrell (2018)
10.1212/01.wnl.0000267643.24870.26
Frontal presentation in progressive supranuclear palsy
L. D. Kaat (2007)
10.1002/mds.25113
Cognitive testing in the diagnosis of parkinsonian disorders: A critical appraisal of the literature
W. Lee (2012)
10.1016/J.ARCHGER.2007.07.005
Cognitive and behavioral assessment in the early stages of neurodegenerative extrapyramidal syndromes.
B. Borroni (2008)
10.1007/978-3-030-14895-9_19
Neuropsychology of Movement Disorders and Motor Neuron Disease: Parkinson’s Disease, Progressive Supranuclear Palsy, Essential Tremor, Huntington’s Disease, and Amyotrophic Lateral Sclerosis
A. Tröster (2019)
10.1007/978-1-4419-1364-7_17
Neuropsychology of Movement Disorders and Motor Neuron Disease
A. Tröster (2010)
10.1016/j.neubiorev.2018.06.014
Executive dysfunction in Parkinson’s disease: A meta-analysis on the Wisconsin Card Sorting Test literature
F. Lange (2018)
10.1002/mds.23023
Clinical and dual‐tasking aspects in frequent and infrequent fallers with progressive supranuclear palsy
U. Lindemann (2010)
10.1016/B978-0-7506-7525-3.50010-8
Behavior and Personality Disturbances
Carissa R. Gehl (2008)
10.1002/mds.22902
Impulsive‐compulsive spectrum behaviors in pathologically confirmed progressive supranuclear palsy
S. O’sullivan (2010)
10.1111/ene.13314
The midbrain‐to‐pons ratio distinguishes progressive supranuclear palsy from non‐fluent primary progressive aphasias
M. Silsby (2017)
10.12740/PP/OnlineFirst/62804
The pattern of verbal, visuospatial and procedural learning in Richardson variant of progressive supranuclear palsy in comparison to Parkinson's disease.
E. Sitek (2017)
See more
Semantic Scholar Logo Some data provided by SemanticScholar