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Journal of the Neurological Sciences
Volume 298, Issue 1
, Pages 70-77
, 15 November 2010
Clinicopathological characteristics of FTLD-TDP showing corticospinal tract degeneration but lacking lower motor neuron loss
References
- . Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes. Acta Neuropathol. 2009;118:349–358
- . Frontotemporal lobar degeneration: clinical and pathological relationships. Acta Neuropathol. 2007;114:31–38
- Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration. Acta Neuropathol. 2007;114:5–22
- Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Am J Pathol. 2008;173:182–194
- Survival profiles of patients with frontotemporal dementia and motor neuron disease. Arch Neurol. 2009;66:1359–1364
- . Is motor neuron disease-inclusion dementia a forme fruste of amyotrophic lateral sclerosis with dementia? An autopsy case further supporting the disease concept. Neuropathology. 2005;25:214–219
- . Neuropathological similarities and differences between frontotemporal lobar degeneration with ubiquitin inclusions and amyotrophic lateral sclerosis with dementia (in Japanese). Brain Nerve. 2009;61:1319–1327
- . Clinical entity of frontotemporal dementia with motor neuron disease. Neuropathology. 2009;29:649–654
- TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. Am J Pathol. 2007;171:227–240
- Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Ann Neurol. 2008;64:60–70
- Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype. Acta Neuropathol. 2006;112:539–549
- Clinical and pathological continuum of multisystem TDP-43 proteinopathies. Arch Neurol. 2009;66:180–189
- . Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions visualized with ubiquitin-binding protein p62 immunohistochemistry. J Neuropathol Exp Neurol. 2008;67:280–298
- TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusions. Arch Neurol. 2007;64:1449–1454
- . In: Gray's Anatomy: The Anatomical Basis of Clinical Practice, Thirty-Ninth edition. United Kingdom: Churchill Livingstone; 2004;p. 397
- . Frontotemporal lobar degeneration with upper motor neuron disease/primary lateral sclerosis. Neurology. 2007;69:1800–1801
- Clinicopathological characterization of Pick's disease versus frontotemporal lobar degeneration with ubiquitin/TDP-43-positive inclusions. Acta Neuropathol. 2009;117:429–444
- . Morphometrical reappraisal of motor neuron system of Pick's disease and amyotrophic lateral sclerosis with dementia. Acta Neuropathol. 2002;104:21–28
- . Reappraisal of Pick's disease. Where should cases of lober atrophy without Pick bodies be placed? (in Japanese). Shinkei Kenkyu no Shinpo. 2001;25:329–341
- . On pyramidal tract lesions in Pick's disease (in Japanese). Seishin Igaku. 1985;27:1171–1178
- Constant involvement of the Betz cells and pyramidal tract in amyotrophic lateral sclerosis with dementia: a clinicopathological study of eight autopsy cases. Acta Neuropathol. 2002;104:249–259
- . Bunina body in frontal lobe dementia without clinical manifestations of motor neuron disease. Acta Neuropathol. 2001;101:281–284
- Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathol. 2009;117:15–18
- . Epidemiology of frontotemporal lobar degeneration. Dement Geriatr Cogn Disord. 2004;17:265–268
- . Neuropathological discrepancy between Japanese Pick's disease without Pick bodies and frontal lobe degeneration type of frontotemporal dementia proposed by Lund and Manchester Group. Neuropathology. 2000;20:76–82
- Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium. Neurology. 2005;65:1863–1872
- . Clinically undetected motor neuron disease in pathologically proven frontotemporal lobar degeneration with motor neuron disease. Arch Neurol. 2006;63:506–512
- . Frontotemporal dementia with ubiquitinated neuronal inclusions presenting with primary lateral sclerosis and parkinsonism: clinicopathological report of an autopsy case. Acta Neuropathol. 2004;107:377–380
- Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases. Acta Neuropathol. 2005;109:353–366
- Pathological heterogeneity of the precentral gyrus in Pick's disease: a study of 16 autopsy cases. Acta Neuropathol. 2006;112:29–42
- . Frontotemporal dementia with cerebral intraneuronal ubiquitin-positive inclusions but lacking lower motor neuron involvement. Acta Neuropathol. 2003;105:81–85
- Atypical progressive supranuclear palsy with corticospinal tract degeneration. J Neuropathol Exp Neurol. 2006;65:396–405
- . Neuropathology. In: Brown RJ, Meininger V, Swash M editor. Amyotrophic lateral sclerosis. 2000;p. 83–112London
- . Amyotrophic lateral sclerosis models and human neuropathology: similarities and differences. Acta Neuropathol. 2008;115:97–114
PII: S0022-510X(10)00362-X
doi: 10.1016/j.jns.2010.08.013
© 2010 Elsevier B.V. All rights reserved.
« Previous
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Journal of the Neurological Sciences
Volume 298, Issue 1
, Pages 70-77
, 15 November 2010
