Results 71 to 80 of about 1,119,241 (175)

Idiopathic inflammatory myopathies

, 2014
Idiopathic inflammatory myopathies (IIMs), except for sporadic inclusion body myositis (sIBM), present with subacute symmetrical weakness of the limb girdle muscles, an elevated serum creatine kinase activity, and inflammatory cells in the muscle biopsy (
Marianne de Visser, de Visser, M., A.J. van der Kooi, Anneke J. van der Kooi, van der Kooi, A. J., M. de Visser   +5 more
core   +1 more source

The mitochondrial‐targeted antioxidant SkQ1 prevents skeletal muscle mitochondrial‐apoptotic but not necroptotic signalling during ovarian cancer

The Journal of Physiology, EarlyView.
Abstract figure legend An evaluation of the degree to which mitochondrial hydrogen peroxide emission (mH2O2)‐mediated apoptotic and necroptotic signalling contributes to skeletal muscle atrophy in an orthotopic epithelial ovarian cancer (EOC) model. To determine whether attenuating mH2O2 could prevent regulated cell death signalling and mitigate muscle
Shahrzad Khajehzadehshoushtar, Luca J. Delfinis, Fasih A. Rahman, Madison C. Garibotti, Shivam Gandhi, Aditya N. Brahmbhatt, Brooke A. Morris, Bianca Garlisi, Sylvia Lauks, Caroline Aitken, Leslie Ogilvie, Zhu‐Xu Zhang, Jeremy A. Simpson, Joe Quadrilatero, Jim Petrik, Christopher G. R. Perry   +15 more
wiley   +1 more source

Cardiac Manifestations in Idiopathic Inflammatory Myopathies: An Overview

, 2019
Idiopathic inflammatory myopathies are a group of autoimmune diseases that are characterized by muscle inflammation resulting in elevated muscle enzyme release and distinctive biopsy findings.
Divya Jayakumar, Rui Zhang, Amy Wasserman, Jayakumar, Divya, Wasserman, Amy, Julia Ash, Zhang, Rui, Ash, Julia   +7 more
core   +1 more source

Nailfold capillaroscopy in idiopathic inflammatory myopathies [PDF]

ARP Rheumatology
Nailfold videocapillaroscopy (NVC) is a non-invasive technique that enables the evaluation of peripheral microcirculation by visualising nailfold capillaries.
Cláudia Pinto Oliveira, Raquel Campanilho Marques, Eduardo Dourado   +2 more
doaj  

A rare case of juvenile dermatomyositis and review of literature

Indian Journal of Paediatric Dermatology, 2017
Idiopathic inflammatory myopathies are rare group of systemic connective tissue diseases. The hallmark of these disorders is symmetrical chronic inflammation and weakness of proximal muscles. Juvenile dermatomyositis (JDM) is the most common inflammatory
Anjali T Bharani, Mohini Harshey, Randhir Khurana, Swati Raipurkar   +3 more
doaj   +1 more source

Prevalence of Systemic Lupus Erythematosus in Australia, 2010–2022: A Population‐Based Study Using Linked National Administrative Health Data

Arthritis Care &Research, Volume 78, Issue 10, Page 1438-1448, October 2026.
Objective Systemic lupus erythematosus (SLE) is a heterogenous inflammatory condition with widely varying global prevalence estimates. The frequency of SLE in the general population of Australia has been reported to be notably lower than contemporary estimates in countries such as the United States or United Kingdom, at 19 to 39 per 100,000 as opposed ...
Lucinda Roper, Rachel Black, Joanna Tieu, Winnie Chen, Matthew Parker, Catherine Hill, Natasha Nassar, Mandana Nikpour   +7 more
wiley   +1 more source

Treatment of idiopathic Inflammatory myopathies

, 2014
Idiopathic inflammatory myopathies are a group of rare, disorders with the primary features of muscle weakness and inflammatory lesions identified in skeletal muscle specimens.
Bercovici, Einav
core  

Dermatomyositis as a Paraneoplastic Syndrome Secondary to Carcinoma of Cervix: A Rare Clinical Association

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Dermatomyositis (DM) is a rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and distinctive cutaneous manifestations. It is frequently associated with underlying malignancies, making recognition of paraneoplastic features crucial.
Manisha Chapagain, Paras Adhikari, Niranjan Pudasaini, Sabin Poudel, Bijay Timilsina   +4 more
wiley   +1 more source

Anti‐U1‐RNP‐Positive Inflammatory Myopathy Presenting With Dysphagia: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT High‐titer anti‐U1‐RNP antibodies may present with myopathy without fulfilling MCTD criteria. We report a 38‐year‐old woman with proximal weakness, elevated muscle enzymes, anti‐U1‐RNP positivity, and inflammatory myopathy on EMG/MRI, but lacking classic overlap features.
Anjlee, Sana Rasheed, Moosa Ashfaq, Simran Bai, Ali Jan Yaqubi, Ahmed Asad Raza   +5 more
wiley   +1 more source

The inflammatory myopathies

, 2013
The inflammatory myopathies are a group of rare conditions that usually present in general practice as a patient with muscle weakness and/or an elevated serum creatine kinase (CK) level.
De Jager, JP
core