Progressive supranuclear palsy: a clinicopathological study of 21 cases

[1]  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.

[2]  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.

[3]  A Albanese,et al.  Some specific clinical features differentiate multiple system atrophy (striatonigral variety) from Parkinson's disease. , 1995, Archives of neurology.

[4]  D. Maraganore,et al.  Progressive supranuclear palsy: neuropathologically based diagnostic clinical criteria. , 1995, Journal of neurology, neurosurgery, and psychiatry.

[5]  N P Quinn,et al.  Clinicopathological study of 35 cases of multiple system atrophy. , 1995, Journal of neurology, neurosurgery, and psychiatry.

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

[7]  I. Ferrier,et al.  An evaluation of the predictive validity and inter‐rater reliability of clinical diagnostic criteria for senile dementia of Lewy body type , 1994, Neurology.

[8]  A. Lees,et al.  Subcortical neurofibrillary degeneration presenting as steele‐richardson‐olszewski and other related syndromes: A review of 90 pathologically verified cases , 1994, Movement disorders : official journal of the Movement Disorder Society.

[9]  C. Duyckaerts,et al.  Cortical tangles in progressive supranuclear palsy. , 1994, Journal of neural transmission. Supplementum.

[10]  E. Tolosa,et al.  Clinical diagnosis and diagnostic criteria of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome). , 1994, Journal of neural transmission. Supplementum.

[11]  J. Brown,et al.  Familial progressive supranuclear palsy. , 1993, Journal of neurology, neurosurgery, and psychiatry.

[12]  H. Morita,et al.  Progressive supranuclear palsy‐like syndrome in two siblings of a consanguineous marriage , 1992, Neurology.

[13]  J. Hughes,et al.  Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. , 1992, Journal of neurology, neurosurgery, and psychiatry.

[14]  P. Lantos.  Neuropathology of unusual dementias: an overview. , 1992, Bailliere's clinical neurology.

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

[16]  C. Duyckaerts,et al.  Constant neurofibrillary changes in the neocortex in progressive supranuclear palsy. Basic differences with Alzheimer's disease and aging , 1990, Neuroscience Letters.

[17]  Y Agid,et al.  Positron emission tomography study in progressive supranuclear palsy. Brain hypometabolic pattern and clinicometabolic correlations. , 1990, Archives of neurology.

[18]  Y. Agid,et al.  Progressive supranuclear palsy: anatomoclinical and biochemical considerations. , 1987, Advances in neurology.

[19]  A. Young,et al.  New form of familial Parkinson‐dementia syndrome , 1983, Neurology.

[20]  K. Jellinger,et al.  Progressive supranuclear palsy: clinico-pathological and biochemical studies. , 1980, Journal of neural transmission. Supplementum.

[21]  J. L. Smith,et al.  Further observations in progressive supranuclear palsy , 1968, Neurology.