Apolipoprotein E alleles in sporadic inclusion‐body myositis and hereditary inclusion‐body myopathy
- 1 August 1996
- journal article
- letter
- Published by Wiley in Annals of Neurology
- Vol. 40 (2), 264
- https://doi.org/10.1002/ana.410400223
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathiesCurrent Opinion in Rheumatology, 1995
- On the metabolism of apolipoprotein E and the Alzheimer diseasesExperimental Neurology, 1995
- Apolipoprotein E type ϵ4 allele frequency is not increased in patients with sporadic inclusion-body myositisNeuroscience Letters, 1995
- Apolipoprotein E immunoreactive deposits in inclusion-body muscle diseasesThe Lancet, 1994
- Association of apolipoprotein E allele ϵ4 with late‐onset familial and sporadic Alzheimer's diseaseNeurology, 1993
- Apolipoprotein E immunoreactivity in cerebral amyloid deposits and neurofibrillary tangles in Alzheimer's disease and kuru plaque amyloid in Creutzfeldt-Jakob diseaseBrain Research, 1991