Literature DB >> 7807140

New pathological findings in amyotrophic lateral sclerosis.

J Lowe1.   

Abstract

There have been recent developments in the pathology of sporadic ALS. A new filamentous neuronal inclusion body in ALS detected by immunohistochemical localisation of the protein ubiquitin has been characterised at the light microscopic and ultrastructural level and appears specific for the disease. The molecular composition of underlying filaments remains unresolved but the quest for this is a major aim in ALS research. Despite being a progressive degenerative process which primarily affects motor systems, ALS is now recognised to involve several non-motor systems and in long survivors affects many subcortical structures. There is also accumulating evidence that the neurodegenerative process underlying ALS may present as a non-motor clinical syndrome, particularly as a frontal lobe dementia with characteristic inclusions present in the non-motor cortex. Considering ALS as a multisystem disease rather than simply a disease of motor neurones has major implications for research into pathogenesis.

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Year:  1994        PMID: 7807140     DOI: 10.1016/0022-510x(94)90175-9

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  21 in total

1.  Amyotrophic Lateral Sclerosis.

Authors: 
Journal:  Curr Treat Options Neurol       Date:  2000-01       Impact factor: 3.598

Review 2.  Disease Mechanisms of C9ORF72 Repeat Expansions.

Authors:  Tania F Gendron; Leonard Petrucelli
Journal:  Cold Spring Harb Perspect Med       Date:  2018-04-02       Impact factor: 6.915

Review 3.  Amyotrophic lateral sclerosis: human challenge for neuroscience.

Authors:  L P Rowland
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-28       Impact factor: 11.205

Review 4.  The relationship between amyotrophic lateral sclerosis and frontotemporal dementia.

Authors:  George M Ringholz; Scott R Greene
Journal:  Curr Neurol Neurosci Rep       Date:  2006-09       Impact factor: 5.081

5.  Potential effect of S-nitrosylated protein disulfide isomerase on mutant SOD1 aggregation and neuronal cell death in amyotrophic lateral sclerosis.

Authors:  Gye Sun Jeon; Tomohiro Nakamura; Jeong-Seon Lee; Won-Jun Choi; Suk-Won Ahn; Kwang-Woo Lee; Jung-Joon Sung; Stuart A Lipton
Journal:  Mol Neurobiol       Date:  2013-10-04       Impact factor: 5.590

Review 6.  Parkinsonism in motor neuron disease: case report and literature review.

Authors:  T L Williams; P J Shaw; J Lowe; D Bates; P G Ince
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

7.  Motor neuron disease with neurofibrillary tangles in a non-Guamanian patient.

Authors:  D A Hilton; S Love; I Ferguson; P Newman
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

8.  Magnetic resonance microscopy and immunohistochemistry of the CNS of the mutant SOD murine model of ALS reveals widespread neural deficits.

Authors:  M S Petrik; J M B Wilson; S C Grant; S J Blackband; R C Tabata; X Shan; C Krieger; C A Shaw
Journal:  Neuromolecular Med       Date:  2007       Impact factor: 3.843

Review 9.  Flightless flies: Drosophila models of neuromuscular disease.

Authors:  Thomas E Lloyd; J Paul Taylor
Journal:  Ann N Y Acad Sci       Date:  2010-01       Impact factor: 5.691

10.  TDP-43 skeins show properties of amyloid in a subset of ALS cases.

Authors:  John L Robinson; Felix Geser; Anna Stieber; Mfon Umoh; Linda K Kwong; Vivianna M Van Deerlin; Virginia M-Y Lee; John Q Trojanowski
Journal:  Acta Neuropathol       Date:  2012-11-03       Impact factor: 17.088

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