Inflammatory features in sporadic late‐onset nemaline myopathy are independent from monoclonal gammo...
Inflammatory features in sporadic late‐onset nemaline myopathy are independent from monoclonal gammopathy
About this item
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Author / Creator
Publisher
Switzerland: John Wiley & Sons, Inc
Journal title
Language
English
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Publication information
Publisher
Switzerland: John Wiley & Sons, Inc
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More information
Scope and Contents
Contents
ABSTRACT
Sporadic late‐onset nemaline myopathy (SLONM) is a rare adult‐onset non‐hereditary disease with subacute proximal muscle and often axial muscle weakness, characterized by the presence of nemaline bodies in skeletal muscle biopsies. Considering its association with concurrent monoclonal gammopathy of undetermined significance (MGUS), the...
Alternative Titles
Full title
Inflammatory features in sporadic late‐onset nemaline myopathy are independent from monoclonal gammopathy
Authors, Artists and Contributors
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8412091
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8412091
Other Identifiers
ISSN
1015-6305
E-ISSN
1750-3639
DOI
10.1111/bpa.12962
