Ubiquitin immunostaining and inclusion body myositis: Study of 30 patients with inclusion body myositis
- 1 August 1997
- journal article
- Published by Elsevier in Human Pathology
- Vol. 28 (8) , 887-892
- https://doi.org/10.1016/s0046-8177(97)90002-2
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Apolipoprotein E ϵ4 in inclusion body myositisAnnals of Neurology, 1995
- Inclusion body myositis and myopathiesAnnals of Neurology, 1995
- Ragged Red Fibers in Normal Aging and Inflammatory MyopathyAnnals of Neurology, 1995
- Rimmed basophilic vacuoles and filamentous inclusions in neuromuscular disordersNeuromuscular Disorders, 1995
- β‐Amyloid precursor epitopes in muscle fibers of inclusion body myositisAnnals of Neurology, 1993
- β-amyloid protein immunoreactivity in muscle of patients with inclusion-body myositisThe Lancet, 1992
- Ubiquitin, cell stress and diseases of the nervous systemNeuropathology and Applied Neurobiology, 1990
- Ubiquitin is a common factor in intermediate filament inclusion bodies of diverse type in man, including those of Parkinson's disease, Pick's disease, and Alzheimer's disease, as well as Rosenthal fibres in cerebellar astrocytomas, cytoplasmic bodies in muscle, and mallory bodies in alcoholic liver diseaseThe Journal of Pathology, 1988
- Rimmed vacuolesActa Neuropathologica, 1980
- Myxovirus-Like Structures in a Case of Human Chronic PolymyositisScience, 1967