Results 11 to 20 of about 12,551,552 (363)

Clinical manifestations in patients with PI*MMMalton genotypes. A matter still unsolved in alpha‐1 antitrypsin deficiency

open access: yesRespirology Case Reports, 2020
We report the genetic variants associated with alpha‐1 antitrypsin deficiency (AATD) in 117 patients admitted to our outpatient clinic and characterized by a serum concentration of AAT lower than 113 mg/dL.
Marina Aiello   +5 more
doaj   +1 more source

Natural history of lung function in spinal muscular atrophy

open access: yesOrphanet Journal of Rare Diseases, 2020
Background Respiratory muscle weakness is an important feature of spinal muscular atrophy (SMA). Progressive lung function decline is the most important cause of mortality and morbidity in patients.
C. Wijngaarde   +14 more
semanticscholar   +1 more source

Muscles and lungs: fatal attraction, but time for intervention

open access: yesMonaldi Archives for Chest Disease, 2005
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J.C. Winck, M. Gonçalves
doaj   +1 more source

Lung functional imaging

open access: yesBreathe, 2023
Pulmonary functional imaging modalities such as computed tomography, magnetic resonance imaging and nuclear imaging can quantitatively assess regional lung functional parameters and their distributions. These include ventilation, perfusion, gas exchange at the microvascular level and biomechanical properties, among other variables.
Sam Bayat, Jim Wild, Tilo Winkler
openaire   +2 more sources

Investigational Treatments in Phase I and II Clinical Trials: A Systematic Review in Asthma

open access: yesBiomedicines, 2022
Inhaled corticosteroids (ICS) remain the mainstay of asthma treatment, along with bronchodilators serving as control agents in combination with ICS or reliever therapy.
Luigino Calzetta   +6 more
doaj   +1 more source

Clinical manifestations of a new alpha‐1 antitrypsin genetic variant: Q0parma

open access: yesRespirology Case Reports, 2022
Alpha‐1 antitrypsin deficiency is an autosomal, codominant disorder caused by mutations of the SERPINA1 gene. Several mutations of SERPINA1 have been described associated with the development of pulmonary emphysema and/or chronic liver disease and ...
Marina Aiello   +9 more
doaj   +1 more source

Stem Cell-Based Regenerative Therapy and Derived Products in COPD: A Systematic Review and Meta-Analysis

open access: yesCells, 2022
COPD is an incurable disorder, characterized by a progressive alveolar tissue destruction and defective mechanisms of repair and defense leading to emphysema.
Luigino Calzetta   +6 more
doaj   +1 more source

Impact of Sex on Proper Use of Inhaler Devices in Asthma and COPD: A Systematic Review and Meta-Analysis

open access: yesPharmaceutics, 2022
Despite females being more often affected by asthma than males and the prevalence of COPD rising in females, conflicting evidence exists as to whether sex may modulate the correct inhaler technique.
Luigino Calzetta   +6 more
doaj   +1 more source

Improving spirometry testing by understanding patient preferences

open access: yesERJ Open Research, 2021
The American Thoracic Society and European Respiratory Society commissioned a task force to update the technical standards for spirometry testing with the aim of increasing the accuracy, precision and quality of spirometry measurements and improving the ...
Barbara Johnson   +3 more
doaj   +1 more source

Caveolins and Lung Function [PDF]

open access: yes, 2012
The primary function of the mammalian lung is to facilitate diffusion of oxygen to venous blood and to ventilate carbon dioxide produced by catabolic reactions within cells. However, it is also responsible for a variety of other important functions, including host defense and production of vasoactive agents to regulate not only systemic blood pressure,
Olga Chernaya   +3 more
openaire   +3 more sources

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