Results 181 to 190 of about 397,364 (338)
Ceftazidime compared with gentamicin and carbenicillin in patients with cystic fibrosis, pulmonary pseudomonas infection, and an exacerbation of respiratory symptoms [PDF]
openalex +1 more source
This work presents a deep learning model to autonomously recognize and classify the secretion retention into three levels for patients receiving invasive mechanical ventilation, achieving 89.08% accuracy. This model can be implemented to ventilators by edge computing, whose feasibility is approved.
Shuai Wang+6 more
wiley +1 more source
Mental health burden in progressive pulmonary fibrosis and idiopathic pulmonary fibrosis: Depression and anxiety. [PDF]
Javorac J+9 more
europepmc +1 more source
1850 FLOW LIMITATION IN INFANTS WITH CYSTIC FIBROSIS DURING A PULMONARY EXACERBATION [PDF]
Robert S. Tepper+4 more
openalex +1 more source
Characterizing the Healthcare Utilization and Costs of Hereditary Hemorrhagic Telangiectasia
ABSTRACT Hereditary hemorrhagic telangiectasia (HHT) is the second‐most common inherited bleeding disorder worldwide, afflicting one in 4000–5000 people, and is the most morbid inherited bleeding disorder of women. HHT causes recurrent severe epistaxis, chronic gastrointestinal bleeding, heavy menstrual bleeding, and arteriovenous malformations in the ...
Hanny Al‐Samkari+5 more
wiley +1 more source
The Fibrosis Across Organs Symposium: A Roadmap for Future Research Priorities. [PDF]
Barnes, Teresa R.+16 more
core +2 more sources
ABSTRACT Cardiovascular complications are the leading cause of mortality in sickle cell anemia (SCA) patients. While extensive data have identified diastolic dysfunction (DD) to increase morbidity and mortality, the unique hemodynamic conditions inherent to SCA challenge the current recommendations to assess diastolic function. Thus, there is an urgent
Théo Simon+20 more
wiley +1 more source
INTERSTITIAL PULMONARY FIBROSIS
William B. Ford+3 more
openaire +3 more sources