Results 121 to 130 of about 3,762 (157)

Profiling of Anti-Signal-Recognition Particle Antibodies and Clinical Characteristics in South Korean Patients With Immune-Mediated Necrotizing Myopathy. [PDF]

open access: yesJ Clin Neurol
Kim SH   +18 more
europepmc   +1 more source

Diffuse Large B-cell Lymphoma Complicated with Anti-3-hydroxy-3-methylglutaryl-Coenzyme A Reductase Immune-mediated Necrotizing Myopathy. [PDF]

open access: yesIntern Med
Tokunaga Y   +10 more
europepmc   +1 more source

Granulomatous myopathy co-existent immune-mediated necrotizing myopathy: A case report

Clinical Neurology and Neurosurgery, 2023
Granulomatous myopathy (GM) is a rare disease characterized by non-caseating inflammation of the skeletal muscle, with sarcoidosis as a common cause. Here, we report a case of GM co-existent immune-mediated necrotizing myopathy (IMNM) in which an anti-signal recognition particle (SRP) antibody was positive and a muscle biopsy showed a non-caseating ...
Danfeng Zheng
exaly   +3 more sources

Immune-mediated necrotizing myopathy (IMNM): A myopathological challenge

Autoimmunity Reviews, 2022
This review is focused on the myopathological spectrum of immune mediated necrotizing myopathies (IMNMs) and its differentiation with other, potentially mimicking, inflammatory and non-inflammatory myopathies. IMNMs are a subgroup of idiopathic inflammatory myopathies (IIMs) characterized by severe clinical presentation with rapidly progressive ...
Merlonghi G., Antonini G., Garibaldi M.
openaire   +2 more sources

Immune-mediated necrotizing myopathy

Zeitschrift für Rheumatologie, 2016
Immune-mediated necrotizing myopathy (IMNM) is a newly identified subgroup of idiopathic inflammatory myopathies. It is defined as a rare and severe disease, with symmetrical and proximal muscle weakness and a characteristic histology. An autoimmune aspect of IMNM is suggested by its association with autoantibodies directed against signal recognition ...
C, Bergua   +6 more
openaire   +2 more sources

Immune-Mediated Necrotizing Myopathy

Journal of Clinical Images
A 70-year-old male with a two-year history of weakness and dysphagia was diagnosed with immune-mediated necrotizing myopathy (IMNM) (Figure 1) confirmed by biopsy and SRP autoantibody positivity.
Wafa Elgeadi Saleh   +1 more
  +5 more sources

Immune‐mediated necrotizing myopathy associated with statins

Muscle & Nerve, 2009
Abstract We report patients from two neuromuscular centers who were evaluated between the years 2000 and 2008 and met the following criteria: (1) proximal muscle weakness occurring during or after treatment with statins; (2) elevated serum creatine kinase (CK); (3) persistence of weakness and elevated CK despite discontinuation of the
Phyllis, Grable-Esposito   +5 more
openaire   +2 more sources

Spectrum of immune-mediated necrotizing myopathies and their treatments

Current Opinion in Rheumatology, 2016
Purpose of reviewThis review aims to describe the spectrum of clinical, histological, and serological features in patients with immune-mediated necrotizing myopathies (IMNMs).Recent findingsAutoantibodies recognizing the signal recognition particle (SRP) or 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) define two unique subtypes of necrotizing ...
Iago, Pinal-Fernandez, Andrew L, Mammen
openaire   +2 more sources

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