An autopsied case of corticobasal degeneration presenting with frontotemporal dementia followed by myoclonus
Author:
Affiliation:
1. Department of Neuropathology, Institute for Medical Science of Aging; Aichi Medical University; Nagakute Japan
2. Department of Neurology; Oyamada Memorial Spa Hospital; Yokkaichi Japan
Publisher
Wiley
Subject
Neurology (clinical),General Medicine,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12398/fullpdf
Reference14 articles.
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2. Office of Rare Diseases of the National Institutes of Health. Office of Rare Diseases neuropathologic criteria for corticobasal degeneration;Dickson;J Neuropathol Exp Neurol,2002
3. Distinct isoforms of tau aggregated in neurons and glial cells in brains of patients with Pick's disease, corticobasal degeneration and progressive supranuclear palsy;Arai;Acta Neuropathol,2001
4. An autopsied case of unclassifiable sporadic four-repeat tauopathy presenting with parkinsonism and speech disturbances;Iwasaki;Neuropathology,2016
5. Relation between clinical findings and progression of cerebral cortical pathology in MM1-type sporadic Creutzfeldt-Jakob disease: proposed staging of cerebral cortical pathology;Iwasaki;J Neurol Sci,2014
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