Results 61 to 70 of about 12,579 (209)

Juvenile idiopathic inflammatory myopathy in a patient with dyskeratosis congenita due to C16orf57 mutation

, 2015
Dyskeratosis congenita (DC) is a rare inherited disorder characterized by reticular skin pigmentation, oral cavity leukoplakia, and nail dystrophy. A variety of noncutaneous (dental, pulmonary, gastrointestinal, neurological, genitourinary, ophthalmic ...

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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

Health-Related Quality of Life (HRQoL) in Idiopathic Inflammatory Myopathy: A Systematic Review.

, 2016
Health-related quality of life (HRQoL) is a research priority in chronic diseases. We undertook a systematic review (registration #CRD42015024939) to identify, appraise and synthesize the evidence relating to HRQoL in idiopathic inflammatory myopathies ...
Malin Regardt, Valérie Leclair, Marie Hudson, Sophie Wojcik, Canadian Inflammatory Myopathy Study (CIMS)   +4 more
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Distinct HLA associations with autoantibody-defined subgroups in idiopathic inflammatory myopathiesResearch in context

EBioMedicine, 2023
Summary: Background: In patients with idiopathic inflammatory myopathies (IIM), autoantibodies are associated with specific clinical phenotypes suggesting a pathogenic role of adaptive immunity.
Valérie Leclair, Angeles S. Galindo-Feria, Simon Rothwell, Olga Kryštůfková, Sepehr Sarrafzadeh Zargar, Herman Mann, Louise Pyndt Diederichsen, Helena Andersson, Martin Klein, Sarah Tansley, Lars Rönnblom, Kerstin Lindblad-Toh, Ann-Christine Syvänen, Marie Wahren-Herlenius, Johanna K. Sandling, Neil McHugh, Janine A. Lamb, Jiri Vencovský, Hector Chinoy, Marie Holmqvist, Matteo Bianchi, Leonid Padyukov, Ingrid E. Lundberg, Lina-Marcela Diaz-Gallo, Matteo Bianchi, Sergey V. Kozyrev, Johanna K. Sandling, Lars Rönnblom, Maija-Leena Eloranta, Ann-Christine Syvänen, Dag Leonard, Johanna Dahlqvist, Maria Lidén, Argyri Mathioudaki, Jennifer RS. Meadows, Jessika Nordin, Gunnel Nordmark, Ingrid E. Lundberg, Antonella Notarnicola, Leonid Padyukov, Anna Tjärnlund, Maryam Dastmalchi, Daniel Eriksson, Øyvind Molberg, Helena Andersson, Kerstin Lindblad-Toh, Fabiana H.G. Farias, Marie Wahren-Herlenius, Awat Jalal, Balsam Hanna, Helena Hellström, Tomas Husmark, Åsa Häggström, Anna Svärd, Thomas Skogh, Louise Pyndt Diederichsen, Janine A. Lamb, Simon Rothwell, Hector Chinoy, Robert G. Cooper, Kerstin Lindblad-Toh, Gerli Rosengren Pielberg, Anna Lobell, Åsa Karlsson, Eva Murén, Kerstin M. Ahlgren, Lars Rönnblom, Maija-Leena Eloranta, Göran Andersson, Nils Landegren, Olle Kämpe, Peter Söderkvis   +71 more
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TRIM Expression and Its Association With Disease Activity in Systemic Lupus Erythematosus

The Kaohsiung Journal of Medical Sciences, EarlyView.
ABSTRACT Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with diverse manifestations, including rash, arthritis, and nephritis. Although autoantibodies are a key feature of SLE, their levels often poorly reflect disease severity, suggesting the involvement of additional contributing factors.
Ling‐Ying Lu, Ling‐Jung Yen, Hui‐Ling Hsia, Zi‐Xeng Weng, Chi‐Hsiang Chung, Paul Wei‐Che Hsu, Chih‐Wei Chiu, Wu‐Chien Chien, Tsung‐Hsien Chang   +8 more
wiley   +1 more source

Anti-SRP myositis: a diagnostic and therapeutic challenge

The Turkish Journal of Pediatrics
Background. Anti-signal recognition protein (anti-SRP) myopathy is a rare idiopathic inflammatory myopathy in children. Herein, a 3-year-old patient with severe anti-SRP myopathy showing a rapidly progressive disease course is presented in order to ...
Merve Cansu Polat, Didem Ardıçlı, Banu Çelikel Acar, Beril Talim, Nesrin Şenbil, Elif Çelikel   +5 more
doaj   +1 more source

The sites and causative organisms of infection in patients with Idiopathic Inflammatory Myopathy admitted to the ICU.

, 2016
The sites and causative organisms of infection in patients with Idiopathic Inflammatory Myopathy admitted to the ICU.
Chan-Yuan Wu (3172446), Qian Wang (32718), Li Weng (460769), Bin Du (138774), Jin-Min Peng (3172440), Xiao-Yun Hu (3172443), Yan Shi (166398)   +6 more
core   +1 more source

Efficacy and safety of intravenous and subcutaneous immunoglobulin therapy in idiopathic inflammatory myopathy: A systematic review and meta-analysis

, 2021
Objective: To perform a systematic review and meta-analysis on the efficacy and safety of intravenous (IVIg) and subcutaneous (SCIg) immunoglobulin (Ig) therapy in the treatment of idiopathic inflammatory myopathy (IIM) and juvenile dermatomyositis (JDM).
Vij, Pallavi, Gelardi, Chiara, Danieli, Maria Giovanna, Haldar, Soumendra Nath, Raaphorst, Joost, Bhadu, Danveer, Goswami, Rudra Prosad, Chatterjee, Moumita, van der Kooi, Anneke J., Kumar, Uma, Lim, Johan   +10 more
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Review of nutrition management of pediatric intestinal pseudo‐obstruction

Nutrition in Clinical Practice, EarlyView.
Abstract Chronic intestinal pseudo‐obstruction (CIPO) is a rare, heterogeneous, and debilitating disorder characterized by profound intestinal dysmotility and severe nutrition challenges. Its presentation resembles that of mechanical bowel obstruction, but CIPO occurs in the absence of luminal obstruction.
Senthilkumar Sankararaman, Raisa Rani James, Bushra El‐Amaireh, Andrea Adler, Kadakkal Radhakrishnan, Sujithra Velayuthan   +5 more
wiley   +1 more source

The advance of idiopathic inflammatory myopathy

Chinese Journal of Contemporary Neurology and Neurosurgery, 2016
DOI: 10.3969/j.issn.1672-6731.2016.10 ...
Yun YUAN
doaj