Idiopathic inflammatory myopathies (IIM), also known as myositis, are a heterogeneous
group of autoimmune disorders with varying clinical manifestations, treatment responses …

The adult and juvenile myositis syndromes, commonly referred to collectively as idiopathic
inflammatory myopathies (IIMs), are systemic autoimmune diseases with the hallmarks of …

Background There is a lack of tools to quantify the response to monoclonal antibodies
(mAbs) holistically in severe uncontrolled asthma patients. Objective To develop a valid …

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 …

Abstract Objective Idiopathic inflammatory myopathies (IIMs) cause proximal muscle
weakness, which affects the ability to carry out the activities of daily living. Wearable physical …

Objective To describe decline in muscle strength and physical function in patients with
sporadic inclusion body myositis (IBM). Methods Manual muscle testing (MMT), quantitative …

Inflammatory neuromuscular disorders encompass a diverse group of immune-mediated
diseases with varying clinical manifestations and treatment responses. The identification of …

Juvenile dermatomyositis (JDM) is a rare heterogeneous immune-medicated condition with
characteristic skin rashes, muscle weakness, vasculopathy, and other organ involvement …

IMNM are muscle-specific autoimmune diseases associated with a severe weakness and a
risk poor muscle strength recovery. Anti-SRP and anti-HMGCR antibodies are specifically …

Background Combined pulmonary fibrosis and emphysema (CPFE) is a novel clinical entity
with a poor prognosis. This study aimed to develop a clinical nomogram model to predict the …