Results 151 to 160 of about 1,177,456 (242)
Expert Perspectives: Defining and Managing Progressive Pulmonary Fibrosis in Systemic Sclerosis
Systemic sclerosis–associated interstitial lung disease (SSc‐ILD) is one of the leading causes of morbidity and mortality in SSc, affecting up to three‐quarters of patients. The disease course is highly heterogeneous, ranging from indolent, nonprogressive forms to rapidly progressive pulmonary fibrosis (PPF).
Devis Benfaremo +7 more
wiley +1 more source
Idiopathic pulmonary fibrosis and interleukins: a bibliometric analysis [1999-2025]. [PDF]
Xu J +5 more
europepmc +1 more source
Abstract Aim Mosliciguat (BAY 1237592), the first soluble guanylate cyclase (sGC) activator in a dry powder inhaler (DPI), could potentially treat pulmonary hypertension with a more targeted delivery than systemic sGC stimulators. We report safety and tolerability of mosliciguat in healthy men.
Johannes Nagelschmitz +7 more
wiley +1 more source
Immunosenescence in Idiopathic Pulmonary Fibrosis. [PDF]
Xiao S +5 more
europepmc +1 more source
ABSTRACT Background Interstitial lung disease (ILD)/pneumonitis is a safety concern with trastuzumab deruxtecan (T‐DXd). We characterized post‐onset changes in ILD severity and imaging patterns, and explored potential prognostic factors for fatal T‐DXd‐related ILD in Japanese patients with breast or gastric cancer.
Shinichi Sasaki +26 more
wiley +1 more source
Background: The crosstalk between autophagy and ferroptosis in pulmonary arterial hypertension (PAH) remains unclear. We investigated the role of FSP1 as a critical link between these processes. Methods and Findings: Mechanistically, we identified that FSP1 degradation is dually regulated by NBR1‐mediated autophagic flux and RNFT1‐dependent K63‐linked ...
Dandan Chen +6 more
wiley +1 more source
Obesity and the risk of idiopathic pulmonary fibrosis: a nationwide population-based study. [PDF]
Kim M, Lee KN, Shin DW, Han K, Lee SW.
europepmc +1 more source
Integrating microfluidic parallel detection with an innate immune extracellular vesicle signature enables rapid active tuberculosis diagnosis from 10 µL of plasma in 30 minutes, effectively discriminating non‐tuberculous respiratory diseases and monitoring treatment response.
Eun Ju Lee +12 more
wiley +1 more source
Idiopathic pulmonary fibrosis with bronchogenic carcinoma
Idiopathic pulmonary fibrosis is essentially a benign disease. We present a case of 65-year-old female patient who presented with left-sided chest pain and breathlessness.
Nair Girija, Swami Shivani, Mehta Ankur
core
Clonal hematopoiesis is associated with progression of idiopathic pulmonary fibrosis. [PDF]
Asarian L +11 more
europepmc +1 more source

