Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration

Rebeiz, 1967, Corticodentatonigral degeneration with neuronal achromasia: A progressive disorder of late adult life, Trans Am Neurol Assoc, 92, 23

10.1007/BF00688042

10.1007/BF00662643

Wang, 1991, Phosphorylated neurofilament epitopes in the achromasic neurons of corticonigral degeneration, Chinese Med J, 104, 1011

Lippa, 1990, Corticonigral degeneration with neuronal achromasia, A clinicopathologic study of two cases. J Neurol Sci, 98, 301

10.1016/0022-510X(94)90072-8

10.1093/brain/112.5.1171

10.1002/ana.410400611

Bergeron, 1997, Cortical degeneration in progressive supranuclear palsy, A comparison with cortical-basal ganglionic degeneration. J Neuropathol Exp Neurol, 56, 726

Bergeron, 1998, Corticobasal ganglionic degeneration and progressive supranuclear palsy presenting with cognitive decline, Brain Pathol, 8, 355, 10.1111/j.1750-3639.1998.tb00159.x

10.1212/WNL.44.11.2015

10.1097/00005072-199601000-00010

10.1212/WNL.48.4.959

10.1212/WNL.55.9.1368

10.1007/s004010050558

10.1212/WNL.53.9.1969

Litvan, 2000, Phenotypes and prognosis: Clinicopathologic studies of corticobasal degeneration, Adv Neurol, 82, 183

10.1212/WNL.53.4.795

10.1001/archneur.55.5.609

10.1007/s004010050934

Takahashi, 1996, Corticobasal degeneration: Widespread argentophilic threads and glia in addition to neurofibrillary tangles, Similarities of cytoskeletal abnormalities in corticobasal degeneration and progressive supranuclear palsy. J Neurol Sci, 138, 66

Matsumoto, 1996, Subcortical neurofibrillary tangles, neuropil threads, and argentophilic glial inclusions in corticobasal degeneration, Clin Neuropathol, 15, 209

10.1016/0304-3940(94)90010-8

10.1007/s004010050911

10.1007/BF00296499

10.1016/0197-4580(91)90022-C

Feany, 1995, Widespread cytoskeletal pathology characterizes corticobasal degeneration, Am J Pathol, 146, 1388

10.1007/BF00294505

10.1007/BF00294503

10.1007/BF00293314

10.1097/00005072-199605000-00001

10.1002/ana.410400204

10.1016/0304-3940(95)11595-N

10.1097/00005072-198605000-00011

Kato, 1992, Ultrastructural and immunohistochemical studies on ballooned cortical neurons in Creutzfeldt-Jakob disease: Expression of alpha B-crystallin ubiquitin and stress-response protein 27, Acta Neuropathol, 84, 443, 10.1007/BF00227673

10.1111/j.1365-2990.1992.tb00796.x

10.1016/0304-3940(96)12612-4

10.1007/s004010050761

Smith, 1992, Immunocytochemical study of ballooned neurons in cortical degeneration with neuronal achromasia, Clin Neuropathol, 11, 28

10.1111/j.1440-1789.1997.tb00047.x

10.1007/BF00294461

10.1159/000114320

Dickson, 1998, Pick's disease, A modern definition. Brain Pathol, 8, 339, 10.1111/j.1750-3639.1998.tb00158.x

10.1136/jnnp.69.6.835

10.1016/S0304-3940(98)00250-X

10.1097/00005072-199601000-00006

10.1007/BF00318574

10.1007/s00401-002-0520-1

10.1016/0006-8993(89)91396-6

10.1097/00002093-199408040-00001

10.1016/S0304-3940(97)00635-6

10.1016/0304-3940(86)90288-0

10.1007/BF00307689

10.1007/BF00310383

Yamada, 1995, Oligodendroglial microtubular massess: An abnormality observed in some human neurodegenerative diseases, Neurosci Lett, 120, 163, 10.1016/0304-3940(90)90028-8

10.1111/j.1365-2990.1989.tb01146.x

10.1097/00005072-199812000-00001

10.1007/s004010050652

10.1007/BF00318575

10.1007/BF00308809

10.1007/s004010051137

Mirra, 1991, The Consortium to Establish a Registry for Alzheimer's Disease (CERAD) Part II, Standardization of the neuropathologic assessment of Alzheimer's disease. Neurology, 41, 479

10.1016/S0197-4580(97)00057-2

10.1007/s004010051135

Hamilton, 2000, Lewy bodies in Alzheimer's disease: A neuropathological review of 145 cases using alpha-synuclein immunohistochemistry, Brain Pathol, 10, 378, 10.1111/j.1750-3639.2000.tb00269.x

Vinters, 2000, Neuropathologic substrates of ischemic vascular dementia, J Neuropathol Exp Neurol, 59, 931, 10.1093/jnen/59.11.931

10.1007/BF00293396

10.1002/1531-8249(200003)47:3<374::AID-ANA15>3.0.CO;2-8

10.1212/WNL.44.11.2015

Oyanagi, 2001, Substantia nigra in progressive supranuclear palsy, corticobasal degeneration, and parkinsonism-dementia complex of Guam: Specific pathological features, J Neuropathol Exp Neurol, 60, 393, 10.1093/jnen/60.4.393

10.1097/00005072-199806000-00006

10.1093/brain/123.5.880

10.1111/j.1365-2990.1989.tb01146.x

Jellinger, 1998, Dementia with grains (argyrophilic grain disease), Brain Pathol, 8, 377, 10.1111/j.1750-3639.1998.tb00161.x

10.1097/00005072-199702000-00006

Togo, 2002, Argyrophilic grain disease is a sporadic 4-repeat tauopathy, J Neuropathol Exp Neurol, 61, 547, 10.1093/jnen/61.6.547

10.1007/s004010050565

10.1093/jnen/60.12.1123

10.1007/BF00309628

Ksiezak-Reding, 1994, Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration, Am J Pathol, 145, 1496

10.1001/archneur.1973.00490290064007

Spillantini, 1998, Frontotemporal dementia and Parkinsonism linked to chromosome 17: A new group of tauopathies, Brain Pathol, 8, 387, 10.1111/j.1750-3639.1998.tb00162.x

10.1111/j.1750-3639.1999.tb00550.x

10.1136/jnnp.65.4.600

10.1093/hmg/8.4.711

10.1212/WNL.56.12.1702