Results 171 to 180 of about 207,794 (393)
Dyskeratosis Congenita Associated Non-Specific Interstitial Pneumonia [PDF]
Dyskeratosis Congenita (DC) is a rare inherited disorder of ectodermal dysplasia. It consists of a classical mucocutaneous triad of abnormal skin pigmentation, nail dystrophy and leukoplakia. Pulmonary disease is seen in 10-15%.
Unnati D. Desai , Jyotsna M. Joshi
doaj
Efectos dun programa de rehabilitación pulmonar en pacientes con fibrosis pulmonar idiopática: unha revisión bibliográfica [PDF]
[Resumen] Objetivo. El objetivo principal de la presente revisión bibliográfica es analizar los efectos de un programa de rehabilitación pulmonar en pacientes diagnosticados de fibrosis pulmonar idiopática (FPI). Material y método.
Pérez Díaz, Andrea
core
ABSTRACT In the 1980s, researchers discovered the remarkable ability of electrospray plumes to effectively ionize gas‐phase molecules via secondary ionization. Around 20 years later—coinciding with the ambient mass spectrometry revolution—secondary electrospray ionization (SESI) and extractive electrospray ionization (EESI) coupled to mass spectrometry
Xin Luo +5 more
wiley +1 more source
Quality of life and dyspnoea in patients treated with bosentan for idiopathic pulmonary fibrosis (BUILD-1) [PDF]
Ganesh Raghu +7 more
openalex +1 more source
ABSTRACT Purpose (i) To assess whether 129Xe apparent diffusion coefficient (ADC) and diffusive length scale (LmD) metrics are quantitatively preserved with deep learning (DL) accelerated acquisition and reconstruction and (ii) to evaluate the feasibility of 129Xe diffusion weighted imaging with natural‐abundance xenon at increased acceleration factors.
Rajagopalan Sundaresan +6 more
wiley +1 more source
HFE gene variants and iron-induced oxygen radical generation in idiopathic pulmonary fibrosis [PDF]
Federica Sangiuolo +18 more
openalex +1 more source
A Proteomics Resource Investigating Fibrosis: Proof‐of‐Concept for Identifying Novel Drug Candidates
ABSTRACT Fibrosis is characterised by inappropriate wound healing and the buildup of excessive fibrous connective tissue, in particular within the extracellular matrix (ECM). This can occur in multiple organs, ultimately leading to organ failure. Despite the high burden of fibrosis, treatment options only delay disease progression.
Hanne Devos +9 more
wiley +1 more source
Clinical implication of protease-activated receptor-2 in idiopathic pulmonary fibrosis [PDF]
Young Sik Park +9 more
openalex +1 more source
ABSTRACT The tyrosine kinase inhibitor, nintedanib, reduces the rate of decline in forced vital capacity (FVC) in a comparable manner in patients with idiopathic pulmonary fibrosis (IPF), other forms of progressive pulmonary fibrosis (PPF), and systemic sclerosis‐associated ILD (SSc‐ILD).
Sonja Hartmann +4 more
wiley +1 more source
ABSTRACT Nintedanib reduces the rate of decline in forced vital capacity (FVC) in adult patients with idiopathic pulmonary fibrosis (IPF), chronic progressive‐fibrosing interstitial lung diseases (ILDs) and systemic sclerosis‐associated ILD (SSc‐ILD).
Sonja Hartmann +4 more
wiley +1 more source

