A harmonized classification system for FTLD-TDP pathology
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J. Trojanowski | V. Lee | D. Mann | I. Mackenzie | E. Jaros | R. Perry | M. Neumann | A. Baborie | Deepak M. Sampathu | D. Plessis
[1] D. Dickson,et al. Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes , 2009, Acta Neuropathologica.
[2] John L. Robinson,et al. Clinical and pathological continuum of multisystem TDP-43 proteinopathies. , 2009, Archives of neurology.
[3] D. Dickson. TDP-43 immunoreactivity in neurodegenerative disorders: disease versus mechanism specificity , 2007, Acta Neuropathologica.
[4] J. Morris,et al. TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. , 2007, The American journal of pathology.
[5] N. Cairns,et al. TDP‐43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations , 2007, Journal of neuropathology and experimental neurology.
[6] D. Neary,et al. Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43 , 2007, Acta Neuropathologica.
[7] Bruce L. Miller,et al. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis , 2006, Science.
[8] J. Trojanowski,et al. Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies. , 2006, The American journal of pathology.
[9] Julie S. Snowden,et al. Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype , 2006, Acta Neuropathologica.
[10] Charles D. Smith,et al. Novel Ubiquitin Neuropathology in Frontotemporal Dementia With Valosin-Containing Protein Gene Mutations , 2006, Journal of neuropathology and experimental neurology.
[11] J. Trojanowski,et al. Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations , 2008, Acta Neuropathologica.