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        157-168 of 174 results for 'Neuromuscular disorders'

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        The association between Staphylococcus aureus and subsequent bronchiectasis in children with cystic fibrosis

        De novo S. aureus acquisition at age 3 is associated with later bronchiectasis and FEF25-75 in children with CF ...

        Research

        Early lung disease in infants and preschool children with cystic fibrosis: What have we learned and what should we do about it?

        This review summarizes what we have learned about early lung disease in children with CF and discusses the implications for clinical practice and research ...

        Research

        Determinants of early-life lung function in African infants

        To assess the determinants of early lung function in African infants. ...

        Research

        Early respiratory infection is associated with reduced spirometry in children with cystic fibrosis

        We hypothesized that the presence of these markers of cystic fibrosis lung disease in the first 2 years of life would be associated with reduced lung... ...

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        Infant respiratory infections and later respiratory hospitalisation in childhood

        The aim of this study was to use total-population based data on an otherwise healthy population of children to assess the relationship between early... ...

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        Structural determinants of long term functional outcomes in young children with cystic fibrosis

        Chest CT identifies children at an early age who have adverse long-term outcomes ...

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        Lung abnormalities do not influence aerobic capacity in school children born preterm

        Children born preterm have impaired lung function and altered lung structure. However, there are conflicting reports on how preterm birth impacts aerobic exercise capacity in childhood. We aimed to investigate how neonatal history and a diagnosis of bronchopulmonary dysplasia (BPD) impact the relationship between function and structure of the lung, and aerobic capacity in school-aged children born very preterm. ...

        Research

        Official ERS technical standard: Global Lung Function Initiative reference values for static lung volumes in individuals of European ancestry

        Measurement of lung volumes across the life course is critical to the diagnosis and management of lung disease. The aim of the study was to use the Global Lung Function Initiative methodology to develop all-age multi-ethnic reference equations for lung volume indices determined using body plethysmography and gas dilution techniques. ...

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        Progressive ventilation inhomogeneity in infants with cystic fibrosis after pulmonary infection

        This study aimed to determine how pulmonary inflammation & infection impacts on ventilation distribution throughout early life in people with cystic fibrosis. ...

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        Lung function trajectories throughout childhood in survivors of very preterm birth: a longitudinal cohort study

        Lung function trajectories are impaired in survivors of very preterm birth ...

        Research

        Effect of posture on lung ventilation distribution and associations with structure in children with cystic fibrosis

        Background: We assessed the effect of posture on ventilation distribution and the impact on associations with structural lung disease. ...

        Research

        Air trapping in early cystic fibrosis lung disease-Does CT tell the full story?

        Mosaic attenuation on expiratory chest computed tomography (CT) is common in early life cystic fibrosis (CF) and often referred to as "air trapping" ...

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