Results 251 to 260 of about 204,699 (375)

Molecular Investigation in Early‐Onset Interstitial Lung Disease: Results From 699 Unrelated Patients

open access: yesRespirology, EarlyView.
ABSTRACT Background and Objective Interstitial lung diseases (ILDs) are rare and severe respiratory conditions that may ultimately result in pulmonary fibrosis (PF). The objective of this study was to present the results of molecular diagnosis of early‐onset ILD (from neonates to young adults < 50 years) in a reference genetic diagnostic laboratory ...
Camille Louvrier   +20 more
wiley   +1 more source

EPDR1 Links Fibroblast Dysfunction to Disease Severity in Idiopathic Pulmonary Fibrosis. [PDF]

open access: yesCells
Lee JU   +7 more
europepmc   +1 more source

The Fibrosis Across Organs Symposium: A Roadmap for Future Research Priorities. [PDF]

open access: yes, 2019
Barnes, Teresa R.   +16 more
core   +2 more sources

World Association for Veterinary Dermatology Consensus Statement for Diagnosis, and Evidence‐Based Clinical Practice Guidelines for Treatment and Prevention of Canine Leishmaniosis

open access: yesVeterinary Dermatology, EarlyView.
Hyperkeratosis of (a) the footpads and (b) the nasal planum. ABSTRACT Background Canine leishmaniosis (CanL) due to Leishmania infantum remains common, and veterinarians do not always follow scientifically sound approaches for diagnosis, treatment and prevention. Objectives To provide consensus guidelines for diagnosis and evidence‐based guidelines for
Manolis N. Saridomichelakis   +9 more
wiley   +1 more source

HDAC11-Mediated Deacetylation of Triosephosphate Isomerase 1 Promotes Idiopathic Pulmonary Fibrosis. [PDF]

open access: yesResearch (Wash D C)
Li Y   +12 more
europepmc   +1 more source

Does interferon- improve pulmonary function in idiopathic pulmonary fibrosis? [PDF]

open access: bronze, 2003
Antje Prasse   +4 more
openalex   +1 more source

Locomotor muscle dysfunction and rehabilitative exercise training in fibrotic interstitial lung disease: Where are we at and where could we go?

open access: yesExperimental Physiology, EarlyView.
Abstract Exercise limitation is a cardinal feature of fibrotic interstitial lung disease arising from pulmonary gas exchange, respiratory mechanical and cardio‐circulatory abnormalities. More recently, it has been recognized that impairment in locomotor muscle function (e.g., reduced muscle mass/strength or heightened fatigability) might also play a ...
Sarah Thivent   +7 more
wiley   +1 more source

<i>SPARC</i> aberrant methylation in idiopathic pulmonary fibrosis: an explorative study. [PDF]

open access: yesFront Cell Dev Biol
Fabrizio FP   +11 more
europepmc   +1 more source

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