Search Results - "Boulé, Michèle"
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1
Longitudinal course of lung function and respiratory muscle strength in spinal muscular atrophy type 2 and 3
Published in European journal of paediatric neurology (01-11-2013)“…Abstract Background Spinal muscular atrophy (SMA) is a common genetic disorder that causes severe hypotonia and weakness, and often fatal restrictive lung…”
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2
Whole pulmonary assessment 1 year after paediatric acute respiratory distress syndrome: prospective multicentre study
Published in Annals of intensive care (20-08-2022)“…Background Long-term pulmonary sequelae, including 1-year thoracic computed tomography (CT) sequelae of paediatric acute respiratory distress syndrome (ARDS)…”
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3
Burkholderia cepacia Is Associated with Pulmonary Hypertension and Increased Mortality among Cystic Fibrosis Patients
Published in Journal of Clinical Microbiology (01-12-2004)“…Article Usage Stats Services JCM Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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4
BAL Fluid Surfactant Protein C Level Is Related to Parenchymal Lung Disease in Children With Sarcoidosis
Published in Chest (01-10-2011)Get full text
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5
Pulmonary Function Tests in Preschool Children with Asthma
Published in American journal of respiratory and critical care medicine (15-09-2003)“…Pulmonary function tests are seldom performed in preschool children with asthma. The aim of this multicenter study was to compare pulmonary function in 74…”
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6
Pulmonary Function Tests in Preschool Children with Cystic Fibrosis
Published in American journal of respiratory and critical care medicine (15-10-2002)“…Pulmonary function tests have rarely been assessed in preschool children with cystic fibrosis (CF). The objective of this multicenter study was to compare…”
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7
Chronic Stridor Caused by Laryngomalacia in Children . Work of Breathing and Effects of Noninvasive Ventilatory Assistance
Published in American journal of respiratory and critical care medicine (15-11-2001)“…Breathing pattern, gas exchange, and respiratory effort were assessed in five awake children with chronic stridor caused by laryngomalacia during spontaneous…”
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8
Nocturnal hypoxaemia and hypercapnia in children with neuromuscular disorders
Published in The European respiratory journal (01-05-2012)“…The aim of the study was to identify daytime predictors of nocturnal gas exchange anomalies in children with neuromuscular disease (NMD) and normal daytime gas…”
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9
Chest Physiotherapy in Cystic Fibrosis: Improved Tolerance With Nasal Pressure Support Ventilation
Published in Pediatrics (Evanston) (01-03-1999)“…Chest physiotherapy (CPT) is an integral part of the treatment of patients with cystic fibrosis (CF). CPT imposes additional respiratory work that may carry a…”
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10
Lung function, diagnosis, and treatment of sleep‐disordered breathing in children with achondroplasia
Published in American journal of medical genetics. Part A (01-08-2012)“…Children with achondroplasia are at risk of sleep‐disordered breathing. The aim of the study was to evaluate lung function and sleep‐disordered breathing in…”
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11
Respiratory Muscle Testing: A Valuable Tool for Children with Neuromuscular Disorders
Published in American journal of respiratory and critical care medicine (01-07-2006)“…Data on respiratory muscle performance in children with neuromuscular disorders are limited. The aim of this study was to assess respiratory muscle strength by…”
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12
Pulmonary function and sleep-related breathing disorders in severely obese children
Published in Clinical nutrition (Edinburgh, Scotland) (01-10-2006)“…To evaluate the frequency of pulmonary function and sleep-breathing disorders in severely obese children and to search for their association with obesity…”
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13
Changes in Pulmonary Mechanics with Increasing Disease Severity in Children and Young Adults with Cystic Fibrosis
Published in American journal of respiratory and critical care medicine (01-07-2002)“…As forced expiratory volume in 1 second (FEV(1)) is a major predictor of outcome in patients with cystic fibrosis (CF), we investigated the effect of FEV(1) on…”
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14
Nutritional status is an important predictor of diaphragm strength in young patients with cystic fibrosis
Published in The American journal of clinical nutrition (01-11-2004)“…The effect of nutritional status and lung disease progression on diaphragm strength in young patients with cystic fibrosis remains unclear. The aim of this…”
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15
Respiratory muscle decline in duchenne muscular dystrophy
Published in Pediatric pulmonology (01-05-2014)“…Summary Objectives Duchenne muscular dystrophy (DMD) causes progressive respiratory muscle weakness. The aim of the study was to analyze the trend of a large…”
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16
Sleep disordered breathing in patients with Prader-Willi syndrome: A multicenter study
Published in Pediatric pulmonology (01-12-2015)“…Summary Objectives Sleep disordered breathing (SDB) is common in patients with Prader–Willi syndrome (PWS) and systematic screening is recommended, especially…”
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17
Respiratory muscle decline in duchenne muscular dystrophy: Respiratory Function in DMD
Published in Pediatric pulmonology (01-05-2014)Get full text
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18
Mechanical limitation during CO2 rebreathing in young patients with cystic fibrosis
Published in Respiratory physiology & neurobiology (27-10-2006)“…The aim of the study was to determine whether a decrease in the ventilatory response to carbon dioxide (CO2) in children with cystic fibrosis (CF) is related…”
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19
Sleep disordered breathing in patients with Prader-Willi syndrome: A multicenter study: Sleep in Prader-Willi Syndrome
Published in Pediatric pulmonology (01-12-2015)Get full text
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20
Sleep disordered breathing in Silver−Russell syndrome patients: a new outcome
Published in Sleep medicine (01-12-2019)“…Imprinting disorders (ID), such as Prader–Willi syndrome (PWS), are associated with sleep-disordered breathing (SDB). No data are available for Silver−Russell…”
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