Aminoacyl-tRNA synthetases: on anti-synthetase syndrome and beyond

AS Galindo-Feria, A Notarnicola, IE Lundberg… - Frontiers in …, 2022 - frontiersin.org
Anti-synthetase syndrome (ASSD) is an autoimmune disease characterized by the presence
of autoantibodies targeting one of several aminoacyl t-RNA synthetases (aaRSs) along with …

[HTML][HTML] Paraneoplastic syndromes associated with lung cancer

N Kanaji, N Watanabe, N Kita, S Bandoh… - World journal of …, 2014 - ncbi.nlm.nih.gov
Paraneoplastic syndromes are signs or symptoms that occur as a result of organ or tissue
damage at locations remote from the site of the primary tumor or metastases. Paraneoplastic …

239th ENMC international workshop: classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018

AL Mammen, Y Allenbach, W Stenzel… - Neuromuscular …, 2020 - Elsevier
Idiopathic inflammatory myopathies (IIM) are a heterogenous family of diseases that can
affect the muscles, skin, lungs, and joints. There have been prior attempts to classify IIMs …

Usefulness of anti‐p155 autoantibody for diagnosing cancer‐associated dermatomyositis: a systematic review and meta‐analysis

E Trallero‐Araguás, JÁ Rodrigo‐Pendás… - Arthritis & …, 2012 - Wiley Online Library
Objective Anti‐p155 autoantibody, which was recently described in adult patients with
dermatomyositis (DM), seems to be associated with cancer in this population. We performed …

Risk of cancer in patients with autoimmune pancreatitis

M Shiokawa, Y Kodama, K Yoshimura… - Official journal of the …, 2013 - journals.lww.com
OBJECTIVES: Although simultaneous occurrences of autoimmune pancreatitis (AIP) and
cancer are occasionally observed, it remains largely unknown whether cancer and AIP …

The RIG-I-like receptor IFIH1/MDA5 is a dermatomyositis-specific autoantigen identified by the anti-CADM-140 antibody

R Nakashima, Y Imura, S Kobayashi, N Yukawa… - …, 2010 - academic.oup.com
Objectives. Various autoantibodies are detected in the sera of PM/DM patients. Some of
them are specific to PM/DM patients and closely associated with clinical manifestations of …

Anti-Jo-1 antibody-positive patients show a characteristic necrotizing perifascicular myositis

L Mescam-Mancini, Y Allenbach, B Hervier… - Brain, 2015 - academic.oup.com
Idiopathic inflammatory myopathies can be classified as polymyositis, dermatomyositis,
immune-mediated necrotizing myopathy, sporadic inclusion body myositis or non-specific …

Paraneoplastic syndromes in rheumatology

B Manger, G Schett - Nature Reviews Rheumatology, 2014 - nature.com
For patients that present with musculoskeletal symptoms, diagnostic procedures carried out
by physicians and rheumatologists are primarily aimed at confirming or excluding the …

Dermatomyositis and polymyositis: clinical presentation, autoantibodies, and pathogenesis

AL Mammen - Annals of the New York Academy of Sciences, 2010 - Wiley Online Library
Dermatomyositis (DM) and polymyositis (PM) are autoimmune myopathies characterized
clinically by proximal muscle weakness, muscle inflammation, extramuscular manifestations …

Idiopathic inflammatory myopathies and malignancy: a comprehensive review

E Tiniakou, AL Mammen - Clinical reviews in allergy & immunology, 2017 - Springer
The idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of autoimmune
diseases (collectively known as myositis) affecting the skeletal muscles as well as other …