Literature DB >> 1376881

Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia.

G Wightman1, V E Anderson, J Martin, M Swash, B H Anderton, D Neary, D Mann, P Luthert, P N Leigh.   

Abstract

Amyotrophic lateral sclerosis (ALS) patients with dementia were found to have ubiquitin-immunoreactive (IR) inclusions in the dentate granule cells of the hippocampus. These inclusions were also present in some patients with minor cognitive changes but otherwise typical ALS. Ubiquitin-IR inclusions were also found in neurons of superficial layers of the frontal and temporal cortex and in the entorhinal cortex in patients with ALS and dementia. These ubiquitin-IR inclusions were non-argyrophilic, and were not labelled by antibodies which identify Alzheimer's neurofibrillary tangles and Pick bodies, nor were they typical of cortical Lewy bodies. Our findings indicate that ubiquitin-IR inclusions in small neurons of the hippocampus, entorhinal area and neocortex are a characteristic feature of degeneration of non-motor cortex in ALS, and are particularly associated with cognitive impairment and dementia of frontal lobe type.

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Year:  1992        PMID: 1376881     DOI: 10.1016/0304-3940(92)90569-s

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  40 in total

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Journal:  J Neuropathol Exp Neurol       Date:  2010-09       Impact factor: 3.685

Review 2.  Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants.

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3.  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.

Authors:  Lionel M Igaz; Linda K Kwong; Yan Xu; Adam C Truax; Kunihiro Uryu; Manuela Neumann; Christopher M Clark; Lauren B Elman; Bruce L Miller; Murray Grossman; Leo F McCluskey; John Q Trojanowski; Virginia M-Y Lee
Journal:  Am J Pathol       Date:  2008-06-05       Impact factor: 4.307

4.  Structural hallmarks of amyotrophic lateral sclerosis progression revealed by probabilistic fiber tractography.

Authors:  Robert Steinbach; Kristian Loewe; Joern Kaufmann; Judith Machts; Katja Kollewe; Susanne Petri; Reinhard Dengler; Hans-Jochen Heinze; Stefan Vielhaber; Mircea Ariel Schoenfeld; Christian Michael Stoppel
Journal:  J Neurol       Date:  2015-07-10       Impact factor: 4.849

Review 5.  Update on recent molecular and genetic advances in frontotemporal lobar degeneration.

Authors:  Eileen H Bigio
Journal:  J Neuropathol Exp Neurol       Date:  2008-07       Impact factor: 3.685

6.  Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer disease.

Authors:  William T Hu; Keith A Josephs; David S Knopman; Bradley F Boeve; Dennis W Dickson; Ronald C Petersen; Joseph E Parisi
Journal:  Acta Neuropathol       Date:  2008-07-01       Impact factor: 17.088

7.  Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis. A longitudinal study in 52 patients.

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Journal:  J Neurol       Date:  2005-03-08       Impact factor: 4.849

8.  Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration.

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Journal:  Acta Neuropathol       Date:  2007-06-20       Impact factor: 17.088

Review 9.  Amyotrophic lateral sclerosis--a model of corticofugal axonal spread.

Authors:  Heiko Braak; Johannes Brettschneider; Albert C Ludolph; Virginia M Lee; John Q Trojanowski; Kelly Del Tredici
Journal:  Nat Rev Neurol       Date:  2013-11-12       Impact factor: 42.937

Review 10.  The role of transactive response DNA-binding protein-43 in amyotrophic lateral sclerosis and frontotemporal dementia.

Authors:  Ian R A Mackenzie; Rosa Rademakers
Journal:  Curr Opin Neurol       Date:  2008-12       Impact factor: 5.710

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