Corticobasal degeneration with primary progressive aphasia and accentuated cortical lesion in superior temporal gyrus: case report and review

[1]  Masanori Kato,et al.  Immunohistochemical investigation of tau-positive structures in the cerebral cortex of patients with progressive supranuclear palsy , 1995, Neuroscience Letters.

[2]  D W Dickson,et al.  Widespread cytoskeletal pathology characterizes corticobasal degeneration. , 1995, The American journal of pathology.

[3]  Ikuyo Fujita,et al.  Corticonigral degeneration with neuronal achromasia presenting with primary progressive aphasia: Ultrastructural and immunocytochemical studies , 1994, Journal of the Neurological Sciences.

[4]  C D Marsden,et al.  Corticobasal degeneration: A clinical study of 36 cases , 1994 .

[5]  Kenji Ikeda,et al.  Argyrophilic thread-like structure in corticobasal degeneration and supranuclear palsy , 1994, Neuroscience Letters.

[6]  Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups. , 1994, Journal of neurology, neurosurgery, and psychiatry.

[7]  N. Nukina,et al.  [Widespread tau abnormality in a case of cortico-basal degeneration]. , 1992, Rinsho shinkeigaku = Clinical neurology.

[8]  F. Cardoso,et al.  Cortico-basal ganglionic degeneration. A case report. , 1992, Arquivos de neuro-psiquiatria.

[9]  K. Kosaka,et al.  Striatopallidonigral degeneration in Pick's disease: a clinicopathological study of 41 cases , 1991, Journal of Neurology.

[10]  P. Mcgeer,et al.  Oligodendroglial microtubular masses: An abnormality observed in some human neurodegenerative diseases , 1990, Neuroscience Letters.

[11]  C. Lippa,et al.  Corticonigral degeneration with neuronal achromasia A clinicopathologic study of two cases , 1990, Journal of the Neurological Sciences.

[12]  P. Ashby,et al.  Cortical‐basal ganglionic degeneration , 1990, Neurology.

[13]  R. A. Crowther,et al.  Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease , 1989, Neuron.

[14]  H. Braak,et al.  CORTICAL AND SUBCORTICAL ARGYROPHILIC GRAINS CHARACTERIZE A DISEASE ASSOCIATED WITH ADULT ONSET DEMENTIA , 1989, Neuropathology and applied neurobiology.

[15]  J. Coyle,et al.  Cortical Degeneration with Swollen Chromatolytic Neurons: Its Relationship to Pick's Disease , 1986, Journal of neuropathology and experimental neurology.

[16]  M. Oda,et al.  Corticobasal degeneration: a disease with widespread appearance of abnormal tau and neurofibrillary tangles, and its relation to progressive supranuclear palsy , 2004, Acta Neuropathologica.

[17]  D. Horoupian,et al.  Unusual case of corticobasal degeneration with tau/Gallyas-positive neuronal and glial tangles , 2004, Acta Neuropathologica.

[18]  T. Uchihara,et al.  Abnormal cytoskeletal pathology peculiar to corticobasal degeneration is different from that of Alzheimer's disease or progressive supranuclear palsy , 2004, Acta Neuropathologica.

[19]  H. Akiyama,et al.  [An autopsy case of corticobasal degeneration clinically misdiagnosed as Pick's disease]. , 1995, Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica.

[20]  Sandra Weintraub,et al.  Primary progressive aphasia: longitudinal course, neuropsychological profile, and language features , 1995 .

[21]  E. Richardson,et al.  Corticodentatonigral degeneration with neuronal achromasia. , 1968, Archives of neurology.

[22]  Thea Lüers,et al.  Pick sche Krankheit , 1957 .