Results 181 to 190 of about 73,410 (327)

Alu Overexpression Leads to an Increased Double‐Stranded RNA Signature in Dermatomyositis

Arthritis &Rheumatology, Volume 78, Issue 1, Page 209-222, January 2026.
Objective Dermatomyositis is an autoimmune condition characterized by a high interferon signature of unknown etiology. Because coding sequences constitute <1.2% of our genomes, there is a need to explore the role of the noncoding genome in disease pathogenesis.
Rayan Najjar, Andrew Mammen, Tomas Mustelin   +2 more
wiley   +1 more source

Beitrag zur Kenntniss der Myositis syphilitica

, 1888
Inga D. Neumann
openalex   +2 more sources

Edematous myositis: a clinical presentation first suggesting dermatomyositis diagnosis [PDF]

, 2020
Mathilde Duchesne, Sarah Léonard-Louis, Océane Landon‐Cardinal, C. Anquetil, K. Mariampillai, Quentin Monzani, Olivier Benvéniste, Yves Allenbach   +7 more
openalex   +1 more source

Radiation myositis

Annals of Oncology, 1999
J S, Welsh, T G, Torre, T L, DeWeese, S, O'Reilly   +3 more
openaire   +2 more sources

Genetic Association Between Polymyositis/Dermatomyositis and Epilepsy: Insights From Mendelian Randomization and Bioinformatic Analyses

Brain and Behavior, Volume 16, Issue 1, January 2026.
This Mendelian randomization study provides robust evidence for a causal link between polymyositis (PM) and epilepsy, highlighting the role of immune‐mediated mechanisms in epilepsy development, while no such association was found for dermatomyositis (DM). Through bioinformatic and statistical analyses, key genes and pathways were identified, with IER3,
Ying Liu, Yuhang Yu, Chulong Fang, Qingzhong Wu, Lingli Ou, Jianhao Xiao, Kui Duan, Ting Jiang, Lan Ye, Xiao Hu, Zhanhui Feng   +10 more
wiley   +1 more source

From Myositis to Electrolyte Crisis: A Case Report of Dengue-Associated Rhabdomyolysis and Salt-Wasting Syndrome [PDF]

Jun Keong Lee, Ru-Fang Tay, Stephanie AP Marianathan, Katrina Kieng Huong Lau, Hui Chin Wong, Thai Lun Tan   +5 more
openalex   +1 more source

Coexistence of anti-HMGCR and anti-MDA5 identified by an unlabeled immunoprecipitation assay in a chinese patient cohort with myositis

, 2018
Li Huang, Li Wang, Yang Yang, Huan Chen, Yanjuan Liu, Ke Liu, Meidong Liu, Yizhi Xiao, Xiaoxia Zuo, Yisha Li, Hui Luo, Huali Zhang, Xianzhong Xiao   +12 more
openalex   +1 more source

A novel surface plasmon resonance approach to assess anti‐dsDNA antibody kinetics and disease severity in systemic lupus erythematosus

Clinical &Translational Immunology, Volume 15, Issue 1, 2026.
An innovative FO‐SPR biosensor for anti‐dsDNA kinetic profiles to differentiate SLE patients with or without nephritis. Maximal FO‐SPR binding correlates with disease activity in lupus nephritis. Abstract Objectives Anti‐dsDNA antibodies are established biomarkers in systemic lupus erythematosus (SLE), yet the clinical utility of conventional assays ...
Carole Nagant, Maxime Taghavi, Hasnae Ben Kacem Ziani, Nathalie Ghorra, Valérie Badot, Sarah Parmentier, Francis Corazza   +6 more
wiley   +1 more source

Anti-NXP2 antibody-associated extensive subcutaneous calcinosis in adult-onset myositis [PDF]

, 2017
Radjiv Goulabchand, Philippe Guilpain, C. Cyteval, Alain Le Quellec   +3 more
openalex   +1 more source

Clinical Characteristics of Patients Initially Suspected of Long COVID: A Case Series From a Specialized Outpatient Clinic

Journal of General and Family Medicine, Volume 27, Issue 1, January 2026.
ABSTRACT Background Sequelae of the acute phase of coronavirus disease 2019 (COVID‐19), termed long COVID, are characterized by a variety of symptoms, including neurological manifestations. Diagnosing long COVID requires excluding alternative conditions that could explain the symptoms.
Masayuki Ohira, Takashi Osada, Hiroaki Kimura, Terunori Sano, Masaki Takao   +4 more
wiley   +1 more source