Results 81 to 90 of about 48,457 (271)

Rheumatoid Arthritis Associated With Anti-Signal Recognition Particle Immune-Mediated Necrotizing Myopathy: A Case Report

Journal of Investigative Medicine High Impact Case Reports
Immune-mediated necrotizing myopathy (IMNM) is a rare subtype of idiopathic inflammatory myopathy that is characterized by severe subacute proximal weakness, myofiber necrosis, and significantly elevated serum creatine kinase.
Mohamed Reda Belkhribchia MD, Johannes Alexander Lobrinus MD, Lamyaa Semlil MD, Nicolas Chauveau MD, Abdelaziz Ajrinija MD, Kristof Egervari MD, Zine Elabidine Ennhaili MD   +6 more
doaj   +1 more source

Neuromuscular disease: 2021 update

Free Neuropathology, 2021
This review highlights ten important advances in the neuromuscular disease field that were first reported in 2020. The overarching topics include (i) advances in understanding of fundamental neuromuscular biology; (ii) new / emerging diseases; (iii ...
Marta Margeta
doaj   +1 more source

Introduction of a novel magnetic resonance imaging-based scoring system for assessing disease activity in children with juvenile dermatomyositis [PDF]

, 2018
Objectives: We aimed to develop and assess the reliability of a novel MRI-based scoring system for reporting the severity of MRI findings in children with suspected JDM.
Adams, Amaka C Offiah, Bohan, Bohan, Brown, Caren Landes, Clarissa Pilkington, Davis, Feldman, Gowdie, Hernandez, Hernandez, Jeannette Kraft, Karl Johnson, Kaufman, Kimball, Love, Lundberg, Maillard, Malattia, Mandela Thyoka, McCann, Oba Adekunle, Owen J Arthurs, Park, Paul Humphries, Pitt, Raj Sinha, Robinson, Stephen Walters, Symmons, Tanimoto, Targoff, Thara Persaud, Van Ness, Walter, Weber   +36 more
core   +2 more sources

Long-term safety of COVID vaccination in individuals with idiopathic inflammatory myopathies: results from the COVAD study [PDF]

, 2023
Bohdana Doskaliuk, R Naveen, Parikshit Sen, Jessica Day, Mrudula Joshi, Arvind Nune, Elena Nikiphorou, Sreoshy Saha, Ai Lyn Tan, Samuel Katsuyuki Shinjo, Nelly Ziadé, Tsvetelina Velikova, Marcin Milchert, Kshitij Jagtap, Ioannis Parodis, Abraham Edgar Gracia‐Ramos, Lorenzo Cavagna, Masataka Kuwana, Johannes Knitza, Yi‐Ming Chen, Ashima Makol, Vishwesh Agarwal, Aarat Patel, John D Pauling, Chris Wincup, Bhupen Barman, Erick Adrian Zamora Tehozol, Jorge Rojas‐Serrano, Ignacio García‐De La Torre, I. J. Colunga-Pedraza, Javier Merayo‐Chalico, Okwara Celestine Chibuzo, Wanruchada Katchamart, Phonpen Akarawatcharangura Goo, Russka Shumnalieva, Leonardo Santos Hoff, Lina El Kibbi, Hussein Halabi, Binit Vaidya, Syahrul Sazliyana Shaharir, A T M Tanveer Hasan, Dzifa Dey, Carlos Enrique Toro Gutiérrez, Carlo V. Caballero‐Uribe, James B Lilleker, Babur Salim, Tamer A. Gheita, Tulika Chatterjee, Oliver Distler, Miguel Ángel Saavedra, Hector Chinoy, Vikas Agarwal, Rohit Aggarwal, Latika Gupta   +53 more
openalex   +1 more source

Atrial Arrhythmias in Cardiac Sarcoidosis—Case Presentation and Systematic Review

Pacing and Clinical Electrophysiology, EarlyView.
ABSTRACT Sarcoidosis is a rare idiopathic, multiorgan disease with clinical cardiac involvement in approximately 5% of cases. Diagnosis and management of cardiac sarcoidosis (CS) have mainly focused on impaired LV function, ventricular arrhythmias, and atrio‐ventricular conduction disease.
Emily C. Hodkinson, Luis Quininir, Edward Hsiao, Rajesh Puranik, Raymond W. Sy   +4 more
wiley   +1 more source

Anti-nuclear matrix protein 2 antibody-positive idiopathic inflammatory myopathies represent extensive myositis without dermatomyositis-specific rash [PDF]

, 2021
Yuki Ichimura, Miwako Shobo, Sae Inoue, Mari Okune, Akemi Maeda, Ryota Tanaka, Noriko Kubota, Isao Matsumoto, Akiko Ishii, Akira Tamaoka, Asami Shimbo, Masaaki Mori, Tomohiro Morio, Takayuki Kishi, Takako Miyamae, Jantima Tanboon, Michio Inoue, Ichizo Nishino, Manabu Fujimoto, Toshifumi Nomura, Naoko Okiyama   +20 more
openalex   +1 more source

Anti-MDA5 juvenile idiopathic inflammatory myopathy: a specific subgroup defined by differentially enhanced interferon-α signalling.

Rheumatology, 2019
OBJECTIVES JDM and juvenile overlap myositis represent heterogeneous subtypes of juvenile idiopathic inflammatory myopathy (JIIM). Chronic evolution can occur in up to 60% of cases, and morbidity/mortality is substantial.
I. Melki, H. Devilliers, C. Gitiaux, V. Bondet, D. Duffy, J. Charuel, M. Miyara, P. Bokov, A. Kheniche, T. Kwon, F. Authier, Y. Allenbach, A. Belot, C. Bodemer, E. Bourrat, Cécile Dumaine, N. Fabien, A. Faye, M. Frémond, A. Hadchouel, Naoki Kitabayashi, A. Lepelley, M. Martin-Niclós, Sasi Mudumba, L. Musset, P. Quartier, G. Rice, L. Seabra, F. Uettwiller, C. Uggenti, S. Viel, M. Rodero, Y. Crow, B. Bader-Meunier   +33 more
semanticscholar   +1 more source

Juvenile Dermatomyositis Triggered by Influenza B: A Case Report on Viral‐Induced Autoimmunity

Pediatric Dermatology, EarlyView.
ABSTRACT A previously healthy 13‐year‐old boy developed juvenile dermatomyositis (JDM) shortly after a confirmed influenza B infection, presenting with progressive proximal muscle weakness and classic cutaneous findings. Laboratory tests revealed elevated muscle enzymes and myositis‐specific autoantibodies, supporting the diagnosis.
Santiago Dans‐Caballero, Miguel Juan‐Cencerrado, Carmen Mochón‐Jiménez, Rosa Roldán‐Molina, Verónica C. Pérez‐Guijo   +4 more
wiley   +1 more source

Studies on the role of autoantibodies and autoantigens in rheumatoid arthritis and myositis [PDF]

, 2016
A major population of patients affected with rheumatoid arthritis (RA) and inflammatory idiopathic myopathies (IIM, collectively called myositis) is characterized by the presence of autoantibodies.
Cerqueira, Cátia
core   +1 more source

Histological heterogeneity in a large clinical cohort of juvenile idiopathic inflammatory myopathy: analysis by myositis autoantibody and pathological features

Neuropathology and Applied Neurobiology, 2019
Juvenile idiopathic inflammatory myopathies have been recently reclassified into clinico‐serological subgroups. Myopathological correlates of the subgroups are incompletely understood.
S. Yasin, P. W. Schutz, C. Deakin, E. Sağ, H. Varsani, S. Simou, L. Marshall, S. Tansley, N. McHugh, J. Holton, L. Wedderburn, T. Jacques, Kate Joe Holly Vanja Joanna Liza Ian Eileen Lou Olivia Armon Ellis‐Gage Roper Briggs Watts McCann Roberts, K. Armon, Joe Ellis‐Gage, H. Roper, Vanja Briggs, Joanna Watts, L. McCann, Ian Roberts, E. Baildam, L. Hanna, O. Lloyd, Susan Wadeson, P. Riley, A. McGovern, C. Ryder, Janis Scott, Beverley Thomas, T. Southwood, E. Al-Abadi, S. Wyatt, G. Jackson, T. Amin, M. Wood, Vanessa VanRooyen, D. Burton, J. Davidson, J. Gardner-Medwin, N. Martin, S. Ferguson, Liz Waxman, Michael Browne, M. Friswell, H. Foster, A. Swift, S. Jandial, Vicky Stevenson, Debbie Wade, E. Sen, E. Smith, Lisa Qiao, S. Watson, Claire Duong, H. Venning, Rangaraj Satyapal, E. Stretton, Mary Jordan, E. Mosley, A. Frost, Lindsay Crate, K. Warrier, Stefanie ord, C. Pilkington, N. Hasson, S. Maillard, Elizabeth Halkon, V. Brown, A. Juggins, Sally Smith, S. Lunt, Elli Enayat, L. Kassoumeri, L. Beard, K. Arnold, Y. Glackin, S. Simou, Beverley Almeida, K. Nistala, R. Marques, Stefanie Dowle, Charis Papadopoulou, Cerise Johnson-Moore, Emily Robinson, K. Murray, J. Ioannou, L. Suffield, M. Al‐Obaidi, Helen Lee, S. Leach, Helen Smith, A. McMahon, H. Chisem, R. Kingshott, N. Wilkinson, Emma K. Inness, E. Kendall, D. Mayers, R. Etherton, Danielle Miller, K. Bailey, J. Clinch, N. Fineman, Helen Pluess-Hall, L. Vallance, Louise Akeroyd, A. Leahy, A. Collier, R. Cutts, Emma Macleod, H. de Graaf, B. Davidson, Sarah Hartfree, D. Pratt   +113 more
semanticscholar   +1 more source