Cognitive and behavioral profile of progressive supranuclear palsy and its phenotypes

[1]  R. V. Kogan,et al.  Multicenter Validation of Metabolic Abnormalities Related to PSP According to the MDS‐PSP Criteria , 2020, Movement disorders : official journal of the Movement Disorder Society.

[2]  M. Silvestrini,et al.  Insight in frontotemporal dementia and progressive supranuclear palsy , 2020, Neurological Sciences.

[3]  A. Boxer,et al.  Cognitive decline on the Repeatable Battery for the Assessment of Neuropsychological Status in progressive supranuclear palsy , 2020, The Clinical neuropsychologist.

[4]  J. Klein,et al.  Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome , 2019, JAMA neurology.

[5]  J. Jankovic,et al.  Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes? , 2019, Parkinsonism & related disorders.

[6]  K. Schulpis,et al.  The Progressive Supranuclear Palsy: Past and Present Aspects , 2019, Clinical gerontologist.

[7]  C. Semenza,et al.  Characteristics and progression of cognitive deficits in progressive supranuclear palsy vs. multiple system atrophy and Parkinson’s disease , 2019, Journal of Neural Transmission.

[8]  W. Oertel,et al.  How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy , 2019, Movement disorders : official journal of the Movement Disorder Society.

[9]  M. T. Pellecchia,et al.  Motor, cognitive and behavioral differences in MDS PSP phenotypes , 2019, Journal of Neurology.

[10]  Peter R. Martin,et al.  Sensitivity and Specificity of Diagnostic Criteria for Progressive Supranuclear Palsy , 2019, Movement disorders : official journal of the Movement Disorder Society.

[11]  A. Boxer,et al.  Cognitive deficits in progressive supranuclear palsy on the Repeatable Battery for the Assessment of Neuropsychological Status , 2019, Journal of clinical and experimental neuropsychology.

[12]  M. T. Pellecchia,et al.  Comparative cognitive and neuropsychiatric profiles between Parkinson’s disease, multiple system atrophy and progressive supranuclear palsy , 2018, Journal of Neurology.

[13]  D. Dickson,et al.  Cognitive impairment in progressive supranuclear palsy is associated with tau burden , 2017, Movement disorders : official journal of the Movement Disorder Society.

[14]  B. Borroni,et al.  Mild Cognitive Impairment and Progression to Dementia in Progressive Supranuclear Palsy , 2017, Neurodegenerative Diseases.

[15]  D. Irwin,et al.  Emerging Diagnostic and Therapeutic Strategies for Tauopathies , 2017, Current Neurology and Neuroscience Reports.

[16]  A. Lang,et al.  Advances in progressive supranuclear palsy: new diagnostic criteria, biomarkers, and therapeutic approaches , 2017, The Lancet Neurology.

[17]  Murray Grossman,et al.  Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria , 2017, Movement disorders : official journal of the Movement Disorder Society.

[18]  T. Robbins,et al.  Apathy and impulsivity in frontotemporal lobar degeneration syndromes , 2016, Brain : a journal of neurology.

[19]  J. Rowe,et al.  Managing cognition in progressive supranuclear palsy , 2016, Neurodegenerative disease management.

[20]  M. Filippi,et al.  Cognitive impairment in progressive supranuclear palsy-Richardson's syndrome is related to white matter damage. , 2016, Parkinsonism & related disorders.

[21]  G. Höglinger,et al.  The phenotypic spectrum of progressive supranuclear palsy. , 2016, Parkinsonism & related disorders.

[22]  D. Neary,et al.  Cognitive–behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia , 2015, Journal of Neurology.

[23]  E. Tolosa,et al.  The phenotypic spectrum of progressive supranuclear palsy: A retrospective multicenter study of 100 definite cases , 2014, Movement disorders : official journal of the Movement Disorder Society.

[24]  J. Hodges,et al.  Cognition in corticobasal syndrome and progressive supranuclear palsy: A review , 2014, Movement disorders : official journal of the Movement Disorder Society.

[25]  I. Litvan,et al.  Behavioral abnormalities in progressive supranuclear palsy , 2013, Psychiatry Research.

[26]  P. Barone,et al.  Abnormal eating behaviors in progressive supranuclear palsy , 2013, European journal of neurology.

[27]  Angie A. Kehagia,et al.  Neuropsychological and clinical heterogeneity of cognitive impairment and dementia in patients with Parkinson's disease , 2010, The Lancet Neurology.

[28]  Y. Agid,et al.  Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy. , 2010, Brain : a journal of neurology.

[29]  B. Borroni,et al.  Pattern of behavioral disturbances in corticobasal degeneration syndrome and progressive supranuclear palsy , 2009, International Psychogeriatrics.

[30]  David R Williams,et al.  Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges , 2009, The Lancet Neurology.

[31]  W. Kamphorst,et al.  Frontal presentation in progressive supranuclear palsy , 2007, Neurology.

[32]  L. Golbe,et al.  A clinical rating scale for progressive supranuclear palsy. , 2007, Brain : a journal of neurology.

[33]  M. Bellgrove,et al.  Loss of insight in frontotemporal dementia, corticobasal degeneration and progressive supranuclear palsy. , 2007, Brain : a journal of neurology.

[34]  G. Halliday,et al.  Comparison of motor, cognitive, and behavioral features in progressive supranuclear palsy and Parkinson's disease , 2006, Movement disorders : official journal of the Movement Disorder Society.

[35]  P. Nichelli,et al.  The Frontal Assessment Battery (FAB): normative values in an Italian population sample , 2005, Neurological Sciences.

[36]  Niall Quinn,et al.  Accuracy of clinical diagnosis of progressive supranuclear palsy , 2004, Movement disorders : official journal of the Movement Disorder Society.

[37]  D. Royall,et al.  The FAB: A frontal assessment battery at bedside , 2001, Neurology.

[38]  D. Burn,et al.  The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK. , 2001, Brain : a journal of neurology.

[39]  I Litvan,et al.  The FAB: A frontal assessment battery at bedside , 2000, Neurology.

[40]  M. Albert.  The subcortical dementia' of progressive supranuclear palsy , 1998 .

[41]  Jeffrey L. Cummings,et al.  Neuropsychiatric aspects of progressive supranuclear palsy , 1996, Neurology.

[42]  A. Lees,et al.  A clinicopathologic study of 100 cases of Parkinson's disease. , 1993, Archives of neurology.

[43]  M. Albert,et al.  The `subcortical dementia' of progressive supranuclear palsy , 1974, Journal of neurology, neurosurgery, and psychiatry.