Results 101 to 110 of about 43,880 (267)

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

Respiratory disorders in patients with polymyositis/dermatomyositis

Современная ревматология, 2014
Idiopathic inflammatory myopathies (IIM) are rare disorders characterized by inflammatory lesions in skeletal muscles. These diseases include polymyositis (PM), dermatomyositis (DM), and inclusion body myositis, which exhibit clinicoimmunological ...
Olga Alekseyevna Antelava, I B Bondarenko, N V Chichasova, E L Насонов   +3 more
doaj   +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

Neutrophil dysregulation is pathogenic in idiopathic inflammatory myopathies.

JCI Insight, 2020
OBJECTIVES Idiopathic inflammatory myopathies (IIM) are characterized by muscle inflammation and weakness, myositis specific autoantibodies (MSAs) and extramuscular organ damage.
N. Seto, J. Torres-Ruíz, C. Carmona-Rivera, I. Pinal-Fernández, I. Pinal-Fernández, K. Pak, M. Purmalek, Y. Hosono, C. Fernandes-Cerqueira, Prateek C. Gowda, N. Arnett, A. Gorbach, O. Benveniste, D. Gómez-Martín, A. Selva-O’Callaghan, J. Milisenda, J. M. Grau-Junyent, L. Christopher‐Stine, F. Miller, I. Lundberg, J. Kahlenberg, Adam Schiffenbauer, A. Mammen, L. Rider, M. Kaplan   +24 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

Apoptosis in idiopathic inflammatory myopathies with partial invasion; a role for CD8+ cytotoxic T cells?

PLoS ONE, 2020
Polymyositis and inclusion body myositis are idiopathic inflammatory myopathies, with a pathology characterized by partial invasion of non-necrotic muscle fibres by CD8+ cytotoxic T-cells, leading to fibre degeneration. Although the main effector pathway
Olof Danielsson, Bo Häggqvist, Liv Gröntoft, Karin Öllinger, Jan Ernerudh, Alfred S. Lewin   +5 more
doaj   +2 more sources

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

Az anti-Jo-1-pozitív antiszintetáz szindróma jellegzetességei gondozott betegeink alapján [PDF]

, 2016
Absztrakt Bevezetés: Az idiopathiás inflammatorikus myopathiák a proximális végtagizmok szimmetrikus gyengeségével jellemezhető szisztémás autoimmun betegségek.
Bodoki, Levente, Dankó, Katalin, Griger, Zoltán, Hodosi, Katalin, Nagy-Vincze, Melinda, Szabó, Katalin   +5 more
core   +1 more source

Where are we moving in the classification of idiopathic inflammatory myopathies?

Current Opinion in Neurology, 2020
Purpose of review Discoveries of myositis-specific antibodies, transcriptomic signatures, and clinicoseropathological correlation support classification of idiopathic inflammatory myopathies (IIM) into four major subgroups: dermatomyositis, immune ...
J. Tanboon, A. Uruha, W. Stenzel, I. Nishino   +3 more
semanticscholar   +1 more source

Exercise modality‐dependent mitochondrial respiratory capacity in satellite cells and conditioned serum‐induced responses in cultured myotubes

Experimental Physiology, EarlyView.
Abstract Exercise‐induced mitochondrial adaptations contribute to muscle function and metabolic health. We aimed to investigate the association of moderate‐intensity swimming (MOD) and high‐intensity interval training (HIIT) with mitochondrial function in skeletal muscle cells treated with exercise‐conditioned serum.
Takanaga Shirai, Hayato Shinkai, Riku Tanimura, Kazuki Uemichi, Shunsuke Sugiyama, Kohei Takeda, Yu Kitaoka, Tohru Takemasa   +7 more
wiley   +1 more source