Results 51 to 60 of about 9,523 (188)

Idiopathic inflammatory myopathies: current insights and future frontiers [PDF]

Idiopathic inflammatory myopathies are a group of autoimmune diseases with a broad spectrum of clinical presentations, primarily characterised by immune-mediated muscle injury.
Gupta, Latika, Fujimoto, Manabu, Paik, Julie J, Machado, Pedro M, Connolly, Caoilfhionn M   +4 more
core   +3 more sources

Imaging assessment of calcinosis in juvenile dermatomyositis: a narrative review

Pediatric Rheumatology Online Journal
Calcinosis is a severe manifestation of juvenile and adult idiopathic inflammatory myopathies, which can lead to pain, limited range of motion, disfigurement, and infection.
Belina Y. Yi, Jessica Perfetto, Evin Rothschild, Kelly Rouster-Stevens, Amanda Robinson, Kathryn Cook, Delaney D. Ding, Andrea Eagle Child, Ovgu Kul Cinar, Barbara Limbach, Charalampia Papadopoulou, Lesley Ann Saketkoo, Adam Schiffenbauer, Heinrike Schmeling, Antonia Valenzuela, Susan Shenoi, Dawn M. Wahezi, for the CARRA JDM Calcinosis workgroup   +17 more
doaj   +1 more source

Sporadic inclusion body myositis in the rheumatology clinic

Indian Journal of Rheumatology, 2020
Sporadic inclusion body myositis (sIBM) is a progressive and insidious skeletal muscle disorder characterized classically by the quadriceps, wrist, and finger flexor weakness.
Fernando Henrique Carlos de Souza, Gustavo Luiz Behrens Pinto, Jean Marcos de Souza, Pablo Arturo Olivo Pallo, Leonardo Santos Hoff, Samuel Katsuyuki Shinjo   +5 more
doaj   +1 more source

Idiopathic Inflammatory Myopathies; Association with Overlap Myositis and Syndromes: Classification, Clinical Characteristics, and Associated Autoantibodies [PDF]

, 2016
Idiopathic inflammatory myopathies (IIM) are traditionally identified as a group of disorders that target skeletal muscle due to autoimmune dysfunction.
Pari Basharat
core  

Atypical presentation of anti-small ubiquitin-like modifier 1 and melanoma differentiation-associated gene 5 antibody positive dermatomyositis presenting with significant inflammatory myopathy on biopsy and normal creatine kinase levels: A case report

SAGE Open Medical Case Reports
Idiopathic inflammatory myopathies are characterized by chronic inflammation of skeletal muscle. The main subtypes of idiopathic inflammatory myopathies include dermatomyositis, polymyositis, and necrotizing autoimmune myopathies.
Srikar Sama, Nidaa Rasheed, Kyle Shen, Negar Khanlou, Karam Han, Alicia Rodriguez-Pla   +5 more
doaj   +1 more source

Miopatías inflamatorias

Revista Médica Clínica Las Condes, 2018
RESUMEN: Las miopatías inflamatorias son un grupo heterogéneo de enfermedades adquiridas del músculo estriado esquelético que comparten la injuria muscular inmunomediada como característica común.
Jorge A. Bevilacqua, MD, PhD, Nicholas Earle, MD   +1 more
doaj   +1 more source

The impact of the COVID-19 pandemic on patients with juvenile idiopathic inflammatory myopathies

Pediatric Rheumatology Online Journal, 2023
Background Throughout the COVID-19 pandemic, there have been concerns regarding the risks of infection in patients with autoimmune disease. In this study, we investigated the impact of the pandemic on patients with juvenile idiopathic inflammatory ...
Dawn M. Wahezi, Dominique Jerome, Evin Rothschild, Belina Yi, Jeffrey Dvergsten, Stacey Tarvin, Susan Kim, Tamar Rubinstein, for the CARRA JDM workgroup   +8 more
doaj   +1 more source

Survival of Patients With Idiopathic Inflammatory Myopathies in Slovenia

Frontiers in Medicine, 2021
Background: Idiopathic inflammatory myopathies (IIMs) are rare systemic diseases associated with significant morbidity and mortality. The aim of our study was to estimate for the first time the survival of IIM patients in Slovenia.Methods: We included ...
Alojzija Hočevar, Alojzija Hočevar, Andrej Viršček, Monika Krošel, Monika Krošel, Suzana Gradišnik, Žiga Rotar, Žiga Rotar, Matija Tomšič, Matija Tomšič, Iztok Holc, Iztok Holc   +11 more
doaj   +1 more source

Immune-Mediated Necrotizing Myopathy: An Often Misdiagnosed Entity

European Journal of Case Reports in Internal Medicine, 2015
Immune-mediated necrotizing myopathies (IMNM) are recognized as a subgroup of idiopathic inflammatory myopathies (IIM). IMNM are defined based on a combination of clinical presentation and laboratory studies, requiring a specific myopathological pattern ...
Joana Almeida Espírito Santo, Rui Garcia, Benilde Barbosa, Olinda Rebelo, José Pereira de Moura   +4 more
doaj   +1 more source

Anti-mitochondrial antibodies are not a hallmark of severity in idiopathic inflammatory myopathies [PDF]

, 2017
International audienceAnti‐mitochondrial antibodies type 2 (AMA2) are the hallmarks of primary biliary cholangitis (PBC) [1]. AMA2 have also been described in 11.3% of idiopathic inflammatory myopathies (IIM) then associatedwith cardiac involvement ...
Mariampillai, Kuberaka, Kuberaka Mariampillai, Lucile Musset, Musset, Lucile, Wladimir Mauhin, Jean-Luc Charuel, Charuel, Jean-Luc, Olivier Benveniste, Mauhin, Wladimir, Allenbach, Yves, Benveniste, Olivier, Yves Allenbach   +11 more
core   +1 more source