, 2004 First published by the Wellcome Trust Centre for the History of Medicine at UCL, 2004. ©The Trustee of the Wellcome Trust, London, 2004. All volumes are freely available online at: www.history.qmul.ac.uk/research/modbiomed/wellcome_witnesses/Annotated ...
Christie, DA, Tansey, EM
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Oral versus inhaled antibiotics for bronchiectasis [PDF]
, 2018 Background Bronchiectasis is a chronic inflammatory disease characterised by a recurrent cycle of respiratory bacterial infections associated with cough, sputum production and impaired quality of life.
Chalmers, James +6 more
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Predictive Factors of Abdominal Compartment Syndrome in Neonatal Age [PDF]
, 2014 In the pediatric population, abdominal compartment syndrome (ACS) is a known complication of abdominal wall defect repair. However, there are only few reports on ACS in newborns and only a proposal of critical intra-abdominal pressure value (IAP) in term
Corsello, G. +7 more
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Журнал микробиологии, эпидемиологии и иммунобиологии, 2015 Aim. Study the spectrum of resistance to antibiotics and its variability of Staphylococcus aureus, Pseudomonas aeruginosa and Вurkholderia cepacia complex (BCC), persisting in lungs of MV patients. Materials and methods. 312 strains of S.
L. R Avetisyan +10 more
doaj
Use of inhaled tobramycin in patients with cystic fibrosis
Терапевтический архив, 2010 The results of a few studies evaluating the efficacy and safety of nebulized tobramycin solution used in patients with cystic fibrosis have been published to date. Pulmonary deposition of inhaled tobramycin and its lung produced concentrations are rather
A G Chermensky, M E Gembitskaya
doaj
IMMUNE PREVENTION OF RESPIRATORY-SYNCYTIAL VIRAL INFECTION: 15 YEARS OF WORLD EXPERIENCE
Педиатрическая фармакология, 2013 The article is dedicated to one of the most important issues of modern neonatology – prevention of respiratory-syncytial virus infection, which is a frequent cause of bronchiolites and pneumoniae in infants and neonates, especially premature infants. The
E. S. Keshishyan
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Cystic Fibrosis Atypical Forms Presentation: Edema, Anemia and Skin Lesions
Revista Finlay, 2021 Cystic fibrosis or mucoviscidosis is the most common genetic disease in the Caucasian race characterized by thickening of secretions due to abnormal ion transport of epithelial cells, manifested with pancreatic insufficiency, progressive lung disease ...
Chabelys de la Caridad Rodríguez Membrides +2 more
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Sleep habits and pattern in 1-14 years old children and relationship with video devices use and evening and night child activities [PDF]
, 2017 Background: Sleep in childhood and adolescence is crucial for mental and physical health; however several researches reported an increasing trend towards a sleep deprivation in this age. Due to the lack of recent epidemiological studies in Italy, the aim
Bernasconi, Sergio +15 more
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A Cross-Sectional Analysis of Paternal Intimacy Problems, Stress Levels, and Satisfaction from Families with Children Born with Mucoviscidosis. [PDF]
Int J Environ Res Public Health, 2022 Popa ZL +6 more
europepmc +1 more source
Polysaccharides and mucin 5AC (MUC5AC) expression in gallbladder mucosa of young patients with gallstones as evaluated by spatial visualization and quantification [PDF]
, 2010 The study aimed at examination of tissue expression of polysaccharides and secretory mucin 5AC (MUC5AC)in young patients (up to 25 years of age) with a symptomatic gallstones.
Agnieszka Adamek +6 more
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