Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges

[1]  Jae-Hong Lee,et al.  Functional brain imaging in pure akinesia with gait freezing: [18F] FDG PET and [18F] FP‐CIT PET analyses , 2009, Movement disorders : official journal of the Movement Disorder Society.

[2]  D. Williams,et al.  How do patients with parkinsonism present? A clinicopathological study , 2009, Internal medicine journal.

[3]  K. Jellinger,et al.  Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration , 1999, Journal of Neurology.

[4]  Peter Heutink,et al.  Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia , 2008, The Lancet Neurology.

[5]  P. Kempster,et al.  Clinical outcomes of progressive supranuclear palsy and multiple system atrophy. , 2008, Brain : a journal of neurology.

[6]  K. Jellinger Different Tau Pathology Pattern in Two Clinical Phenotypes of Progressive Supranuclear Palsy , 2008, Neurodegenerative Diseases.

[7]  G. Halliday,et al.  Excessive dopamine neuron loss in progressive supranuclear palsy , 2008, Movement disorders : official journal of the Movement Disorder Society.

[8]  A. Lees,et al.  The auditory startle response in parkinsonism may reveal the extent but not type of pathology , 2008, Journal of Neurology.

[9]  A. Lees,et al.  J. Clifford Richardson and 50 years of progressive supranuclear palsy , 2008, Neurology.

[10]  D. Dickson,et al.  Clinical and neuropathologic features of progressive supranuclear palsy with severe pallido-nigro-luysial degeneration and axonal dystrophy. , 2008, Brain : a journal of neurology.

[11]  A. Lees,et al.  Pure akinesia with gait freezing: A third clinical phenotype of progressive supranuclear palsy , 2007, Movement disorders : official journal of the Movement Disorder Society.

[12]  E. Tolosa,et al.  Long lasting pure freezing of gait preceding progressive supranuclear palsy: A clinicopathological study , 2007, Movement disorders : official journal of the Movement Disorder Society.

[13]  A. Lees,et al.  Using the presence of visual hallucinations to differentiate Parkinson’s disease from atypical parkinsonism , 2007, Journal of Neurology, Neurosurgery, and Psychiatry.

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

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

[16]  A. Lees,et al.  Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome. , 2007, Brain : a journal of neurology.

[17]  T. Révész,et al.  Genetic variation at the tau locus and clinical syndromes associated with progressive supranuclear palsy , 2007, Movement disorders : official journal of the Movement Disorder Society.

[18]  D. Williams,et al.  Tauopathies: classification and clinical update on neurodegenerative diseases associated with microtubule‐associated protein tau , 2006, Internal medicine journal.

[19]  Jennifer L. Whitwell,et al.  Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech. , 2006, Brain : a journal of neurology.

[20]  R. Walker,et al.  The Prevalence of Parkinson’s Disease in an Area of North Tyneside in the North-East of England , 2006, Neuroepidemiology.

[21]  A. Lees,et al.  Predictors of falls and fractures in bradykinetic rigid syndromes: a retrospective study , 2006, Journal of Neurology, Neurosurgery & Psychiatry.

[22]  S. Factor,et al.  Primary progressive freezing gait: A syndrome with many causes , 2006, Neurology.

[23]  Joseph James Duffy,et al.  Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP , 2006, Neurology.

[24]  L. Golbe,et al.  Progressive supranuclear palsy , 2001, Harvard women's health watch.

[25]  M. Hasegawa,et al.  Tau-Positive Fine Granules in the Cerebral White Matter: A Novel Finding Among the Tauopathies Exclusive to Parkinsonism-Dementia Complex of Guam , 2005, Journal of neuropathology and experimental neurology.

[26]  Andrew J Lees,et al.  Atypical unclassifiable parkinsonism on Guadeloupe: An environmental toxic hypothesis , 2005, Movement disorders : official journal of the Movement Disorder Society.

[27]  B. Boeve,et al.  Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome , 2005, Movement disorders : official journal of the Movement Disorder Society.

[28]  Joseph James Duffy,et al.  Atypical progressive supranuclear palsy underlying progressive apraxia of speech and nonfluent aphasia , 2005, Neurocase.

[29]  A. Bronstein,et al.  Clinical grand round: A rapidly progressive pyramidal and extrapyramidal syndrome with a supranuclear gaze palsy , 2005, Movement disorders : official journal of the Movement Disorder Society.

[30]  Beatriz Rico,et al.  The Primate Thalamus Is a Key Target for Brain Dopamine , 2005, The Journal of Neuroscience.

[31]  N. Quinn,et al.  Progressive supranuclear palsy‐like phenotype associated with bilateral hypoxic–ischemic striopallidal lesions , 2005, Movement disorders : official journal of the Movement Disorder Society.

[32]  Nicola Pavese,et al.  Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1 , 2005, Annals of neurology.

[33]  U Nath,et al.  Population based mortality and quality of death certification in progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) , 2005, Journal of Neurology, Neurosurgery & Psychiatry.

[34]  A J Lees,et al.  Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration , 2005, Journal of Medical Genetics.

[35]  Y. Takanashi,et al.  Discrepancy between clinical and pathological diagnoses of CBD and PSP , 2005, Journal of Neurology.

[36]  T. Robbins,et al.  Heterogeneity of Parkinson’s disease in the early clinical stages using a data driven approach , 2005, Journal of Neurology, Neurosurgery & Psychiatry.

[37]  D. Paviour,et al.  Commentary on: Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism, by , 2005 .

[38]  Thomas Meitinger,et al.  Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology , 2004, Neuron.

[39]  A. Godbolt,et al.  Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: broadening the clinical picture to include progressive supranuclear palsy. , 2004, Brain : a journal of neurology.

[40]  J. Hodges,et al.  Clinicopathological correlates in frontotemporal dementia , 2004, Annals of neurology.

[41]  J. Matsumoto,et al.  Syndrome resembling PSP after surgical repair of ascending aorta dissection or aneurysm , 2004, Neurology.

[42]  Hitoshi Takahashi,et al.  Pathological heterogeneity in progressive supranuclear palsy and corticobasal degeneration , 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.

[43]  Y. Mizuno,et al.  Glial localization of four‐repeat tau in atypical progressive supranuclear palsy , 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.

[44]  E. Cochran,et al.  Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders , 2004 .

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

[46]  Michel Goedert,et al.  Tau protein and neurodegeneration. , 2004, Seminars in cell & developmental biology.

[47]  D. Dickson,et al.  Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders: Dickson/Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders , 2011 .

[48]  J. Ahlskog,et al.  Progressive supranuclear palsy phenotype secondary to CADASIL. , 2003, Parkinsonism & related disorders.

[49]  N. Quinn,et al.  Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP , 2003, Neurology.

[50]  J. Holton,et al.  Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule‐binding repeat domains as demonstrated by new specific monoclonal antibodies , 2003, Neuropathology and applied neurobiology.

[51]  Y Ben-Shlomo,et al.  Clinical features and natural history of progressive supranuclear palsy , 2003, Neurology.

[52]  S. Leurgans,et al.  Progression of gait, speech and swallowing deficits in progressive supranuclear palsy , 2003, Neurology.

[53]  M. Husain,et al.  Cerebral amyloid angiopathy and motor neurone disease presenting with a progressive supranuclear palsy‐like syndrome , 2003, Movement disorders : official journal of the Movement Disorder Society.

[54]  D. Zamir,et al.  Primary antiphospholipid antibody syndrome masquerading as progressive supranuclear palsy , 2003, Lupus.

[55]  P. Lantos,et al.  Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration , 2002, Journal of neuropathology and experimental neurology.

[56]  C. Robinson,et al.  Progressive supranuclear palsy diagnosis and confounding features: Report on 16 autopsied cases , 2002, Movement disorders : official journal of the Movement Disorder Society.

[57]  John Q Trojanowski,et al.  An R5L τ mutation in a subject with a progressive supranuclear palsy phenotype , 2002, Annals of neurology.

[58]  D. Dickson,et al.  A clinicopathological study of vascular progressive supranuclear palsy: a multi-infarct disorder presenting as progressive supranuclear palsy. , 2002, Archives of neurology.

[59]  F. Lepore Procerus sign in progressive supranuclear palsy , 2002, Neurology.

[60]  T Lashley,et al.  Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy. , 2002, Brain : a journal of neurology.

[61]  Yoav Ben-Shlomo,et al.  The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. , 2002, Brain : a journal of neurology.

[62]  Charles Duyckaerts,et al.  Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy. , 2002, Brain : a journal of neurology.

[63]  M. Rossor,et al.  Sequence analysis of tau in familial and sporadic progressive supranuclear palsy , 2002, Journal of neurology, neurosurgery, and psychiatry.

[64]  Hitoshi Takahashi,et al.  Progressive supranuclear palsy on Guam , 2001, Acta Neuropathologica.

[65]  M. Fulham,et al.  Corticobasal syndrome with tau pathology , 2001, Movement disorders : official journal of the Movement Disorder Society.

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

[67]  K. Ikeda,et al.  Substantia Nigra in Progressive Supranuclear Palsy, Corticobasal Degeneration, and Parkinsonism‐Dementia Complex of Guam: Specific Pathological Features , 2001, Journal of neuropathology and experimental neurology.

[68]  E. Tolosa,et al.  Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene , 2001, Annals of neurology.

[69]  M. Tabaton,et al.  Neurosyphilis presenting as progressive supranuclear palsy , 2000, Movement disorders : official journal of the Movement Disorder Society.

[70]  P. Schofield,et al.  Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene , 2000 .

[71]  M. Vidailhet,et al.  Longitudinal ocular motor study in corticobasal degeneration and progressive supranuclear palsy , 2000, Neurology.

[72]  D. Perl,et al.  Parkinsonism, dementia and vertical gaze palsy in a Guamanian with atypical neuroglial degeneration , 2000, Acta Neuropathologica.

[73]  P. Schofield,et al.  Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations. , 2000, Brain : a journal of neurology.

[74]  Y Ben-Shlomo,et al.  Prevalence of progressive supranuclear palsy and multiple system atrophy: a cross-sectional study , 1999, The Lancet.

[75]  S. McDonnell,et al.  Autopsy patterns for Parkinson’s disease and related disorders in Olmsted County, Minnesota , 1999, Neurology.

[76]  R. Petersen,et al.  Highly active antiretroviral therapy reverses brain metabolite abnormalities in mild HIV dementia , 1999, Neurology.

[77]  R. Leigh,et al.  Whipple’s disease mimicking progressive supranuclear palsy: the diagnostic value of eye movement recording , 1999, Journal of neurology, neurosurgery, and psychiatry.

[78]  M. Freedman,et al.  Frontotemporal lobar degeneration , 1998, Neurology.

[79]  I Litvan,et al.  Progressive supranuclear palsy , 1998, Neurology.

[80]  D. Maraganore,et al.  Incidence of progressive supranuclear palsy and multiple system atrophy in Olmsted County, Minnesota, 1976 to 1990 , 1997, Neurology.

[81]  I Litvan,et al.  Progressive supranuclear palsy and corticobasal degeneration. , 2011 .

[82]  T. Chase,et al.  Distinct Pathological Features of the Gallyas‐ and Tau‐positive Glia in the Parkinsonism‐Dementia Complex and Amyotrophic Lateral Sclerosis of Guam , 1997, Journal of neuropathology and experimental neurology.

[83]  M. Hallett,et al.  Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) , 1996, Neurology.

[84]  I Litvan,et al.  Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) , 1996, Neurology.

[85]  R. Leigh,et al.  Dynamic properties of horizontal and vertical eye movements in parkinsonian syndromes , 1996, Annals of neurology.

[86]  I Litvan,et al.  Validity and Reliability of the Preliminary NINDS Neuropathologic Criteria for Progressive Supranuclear Palsy and Related Disorders , 1996, Journal of neuropathology and experimental neurology.

[87]  A. Lees,et al.  A case of progressive subcortical gliosis associated with deposition of abnormal prion protein (PrP) , 1995, Journal of neurology, neurosurgery, and psychiatry.

[88]  V. Bruin,et al.  The clinical and pathological spectrum of Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy): a reappraisal. , 1995, Brain : a journal of neurology.

[89]  I Litvan,et al.  Preliminary NINDS neuropathologic criteria for Steele‐Richardson‐Olszewski syndrome (progressive supranuclear palsy) , 1994, Neurology.

[90]  R. Leigh,et al.  The syndrome of 'pure akinesia' and its relationship to progressive supranuclear palsy , 1994, Neurology.

[91]  M. Al‐Hakim,et al.  Parkinson's Disease and Movement Disorders, 2nd Ed. , 1994, Neurology.

[92]  R. Garruto,et al.  Rare neuropil threads in amyotrophic lateral sclerosis and parkinsonism-dementia on Guam and in the Kii Peninsula of Japan. , 1993, Dementia.

[93]  I. Kanazawa,et al.  Progressive supranuclear palsy presenting with pure akinesia. , 1993, Advances in neurology.

[94]  Richard S. J. Frackowiak,et al.  Diffuse Lewy body disease presenting with a supranuclear gaze palsy. , 1991, Journal of neurology, neurosurgery, and psychiatry.

[95]  L Lavine,et al.  Supranuclear disturbances of ocular motility in Lytico‐Bodig , 1988, Neurology.

[96]  J. Haxby,et al.  NIH conference. Alzheimer disease: clinical and biological heterogeneity. , 1988, Annals of internal medicine.

[97]  T. H. Burnstine,et al.  Movement Disorders 2 , 1988, Neurology.

[98]  J. Jankovic,et al.  Parkinson's Disease and Movement Disorders , 1988 .

[99]  A. Yasuhara,et al.  Blink reflex elicited by auditory stimulation in the rabbit , 1986, Journal of the Neurological Sciences.

[100]  A. Lees,et al.  The clinical features and natural history of the Steele‐Richardson‐Olszewski syndrome (progressive supranuclear palsy) , 1986, Neurology.

[101]  R. Leigh,et al.  The neurology of eye movements , 1984 .

[102]  B. Neville,et al.  A neurovisceral storage disease with vertical supranuclear ophthalmoplegia, and its relationship to Niemann-Pick disease. A report of nine patients. , 1973, Brain : a journal of neurology.

[103]  M. Parma,et al.  [The Steele-Richardson-Olszewski syndrome (or "progressive supranuclear palsy")]. , 1968, Minerva medica.

[104]  E. Richardson,et al.  Corticodentatonigral degeneration with neuronal achromasia: a progressive disorder of late adult life. , 1967, Transactions of the American Neurological Association.

[105]  J. Olszewski,et al.  Progressive Supranuclear Palsy: A Heterogeneous Degeneration Involving the Brain Stem, Basal Ganglia and Cerebellum With Vertical Gaze and Pseudobulbar Palsy, Nuchal Dystonia and Dementia , 1964 .

[106]  J. Olszewski,et al.  SUPRANUCLEAR OPHTHALMOPLEGIA, PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA. A CLINICAL REPORT ON EIGHT CASES OF "HETEROGENOUS SYSTEM DEGENERATION". , 1963, Transactions of the American Neurological Association.