Results 231 to 240 of about 195,645 (350)
Correspondence to: Clinico‐sero‐pathological characteristics of anti‐Ha antisynthetase syndrome
Brain Pathology, EarlyView.
Marie‐Therese Holzer+5 more
wiley +1 more source
ABSTRACT Background and Objective The available evidence on the effects of ambulatory oxygen on exercise impairment in patients with fibrotic interstitial lung diseases (F‐ILD) is of limited quality. Methods We conducted a randomised, double‐blind, placebo‐controlled crossover trial with 32 normoxaemic F‐ILD patients, desaturating to ≤ 88% during a ...
Giuseppina Ciarleglio+7 more
wiley +1 more source
Delving Deeper into Genotypic-Phenotypic Associations in Idiopathic Pulmonary Fibrosis. [PDF]
Montesi SB, Adegunsoye A.
europepmc +1 more source
ABSTRACT Background and Objective The diagnosis of interstitial lung diseases (ILDs) often relies on the integration of various clinical, radiological, and histopathological data. Achieving high diagnostic accuracy in ILDs, particularly for distinguishing usual interstitial pneumonia (UIP), is challenging and requires a multidisciplinary approach ...
Kris Lami+25 more
wiley +1 more source
A Twist in the Fibrotic Tale: The Overlooked Vasculopathy in Idiopathic Pulmonary Fibrosis. [PDF]
Tonelli AR, Sahay S.
europepmc +1 more source
Living with idiopathic pulmonary fibrosis [PDF]
openaire +3 more sources
ABSTRACT Background and Objective Idiopathic pulmonary fibrosis is a progressive interstitial lung disease characterised by excessive activation of myofibroblasts. However, currently available antifibrotic drugs exhibit limited efficacy. The dysregulation of redox processes plays a significant role in the pathogenesis of idiopathic pulmonary fibrosis ...
Jie Huang+12 more
wiley +1 more source
Malnutrition, Sarcopenia, and Malnutrition Sarcopenia Syndrome in Idiopathic Pulmonary Fibrosis. [PDF]
Cabrera-César E+12 more
europepmc +1 more source