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Inflammatory myopathies after allogeneic stem cell transplantation
Discussion: Among recipients of allo ‐SCT, weakness is common, and the incidence of IM is increased. Histopathological diagnoses are varied, and we report findings of necrotizing myopathy and anti‐MDA5‐associated DM.Muscle Nerve, 2018
Source: Muscle and Nerve - November 20, 2018 Category: Internal Medicine Authors: Julia New ‐Tolley, Caroline Smith, Barbara Koszyca, Sophia Otto, Adam Maundrell, Peter Bardy, Devendra Hiwase, Agnes S. M. Yong, Ian Lewis, Vidya Limaye Tags: Clinical Research Source Type: research

Ischemic myopathy revealing systemic calciphylaxis
This article is protected by copyright. All rights reserved.
Source: Muscle and Nerve - December 8, 2016 Category: Internal Medicine Authors: Jessie Aouizerate, Laurence Valleyrie ‐Allanore, Nicolas Limal, S. Samar Ayache, Romain K. Gherardi, Vincent Audard, François Jérôme Authier Tags: Research Article Source Type: research

Sporadic late‐onset nemaline myopathy as a rare cause of slowly progressive muscle weakness with young adult onset
Conclusions: Considering the recent reports of successful treatment of SLONM, early and correct diagnosis of SLONM associated with monoclonal gammopathy is important. SLONM should be added to the list of diseases to consider in the differential diagnosis of progressive muscle weakness with young adult onset. © 2014 Wiley Periodicals, Inc.
Source: Muscle and Nerve - November 1, 2014 Category: Internal Medicine Authors: Meiko Hashimoto Maeda, Hikari Ohta, Koji Izutsu, Jun Shimizu, Yoshikazu Uesaka Tags: Case of the Month Source Type: research

Sporadic late onset nemaline myopathy and immunoglobulin deposition disease
Discussion: We speculate that deposition of light and heavy chains, rather than nemaline bodies, has myotoxic effects on skeletal muscle. © 2013 Wiley Periodicals, Inc.
Source: Muscle and Nerve - July 19, 2013 Category: Internal Medicine Authors: Kathrin Doppler, Stefan Knop, Hermann Einsele, Claudia Sommer, Carsten Wessig Tags: Case of the Month Source Type: research