Works matching IS 87556863 AND DT 2022 AND VI 57 AND IP 7
Results: 42
HIDEA syndrome: A rare cause of congenital hypoventilation in a premature infant.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1826, doi. 10.1002/ppul.25966
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Foreign body aspiration in two young infants: The devil in the carpet.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1795, doi. 10.1002/ppul.25965
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Diagnostic accuracy of point‐of‐care ultrasound compared to standard‐of‐care methods for endotracheal tube placement in neonates.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1744, doi. 10.1002/ppul.25955
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COVID‐19 infection and nocardiosis causing the death of an adolescent with cystic fibrosis.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1823, doi. 10.1002/ppul.25954
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Asthma risk after a pediatric intensive care unit admission for respiratory syncytial virus bronchiolitis.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1677, doi. 10.1002/ppul.25953
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Indication‐based timing of tracheostomy and its effects on outcome in the pediatric intensive care unit.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1684, doi. 10.1002/ppul.25952
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Phosphatidylethanolamines as biomarkers of e‐cigarette or vaping product use‐associated lung injury.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1792, doi. 10.1002/ppul.25951
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- Article
Elevated serum TARC/CCL17 levels associated with childhood interstitial lung disease with SFTPC gene mutation.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1820, doi. 10.1002/ppul.25950
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Obesity is a risk factor for decrease in lung function after COVID‐19 infection in children with asthma.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1668, doi. 10.1002/ppul.25949
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Cystic fibrosis year in review 2021.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1590, doi. 10.1002/ppul.25948
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Delayed tension hemothorax after chest trauma in children.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1818, doi. 10.1002/ppul.25947
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Pharmacist‐administered audiology screening for pediatric cystic fibrosis patients exposed to high‐dose aminoglycosides: A pilot study.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1814, doi. 10.1002/ppul.25946
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Primary ciliary dyskinesia and fungal infections: Two cases of allergic bronchopulmonary aspergillosis in children.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1809, doi. 10.1002/ppul.25945
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Comparison of clinical features of COVID‐19 infection in children with asthma and their healthy peers.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1693, doi. 10.1002/ppul.25937
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Pulmonary embolism in adolescent with COVID‐19 during aromatase inhibitor therapy.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1789, doi. 10.1002/ppul.25944
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Cystic fibrosis‐related liver disease is an independent risk factor for mortality and increased health care resource utilization in hospitalized pediatric patients with cystic fibrosis.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1717, doi. 10.1002/ppul.25941
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Impaired ventilation during 6‐min walk test in congenital central hypoventilation syndrome.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1660, doi. 10.1002/ppul.25940
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DNA sequencing analysis of cystic fibrosis transmembrane conductance regulator gene identifies cystic fibrosis‐associated variants in the Severe Asthma Research Program.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1782, doi. 10.1002/ppul.25939
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At‐home compounding preparation of slow desensitization of elexacaftor/tezacaftor/ivacaftor for delayed hypersensitivity rash.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1779, doi. 10.1002/ppul.25938
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Use of inhaled antibiotics among Danish patients with cystic fibrosis.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1726, doi. 10.1002/ppul.25942
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A pneumothorax in the setting of COVID‐19 associated pneumatoceles in a pediatric patient.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1806, doi. 10.1002/ppul.25936
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Postdischarge health resource use in pediatric survivors of prolonged mechanical ventilation for acute respiratory illness.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1651, doi. 10.1002/ppul.25934
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Insurance coverage and respiratory morbidities in bronchopulmonary dysplasia.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1735, doi. 10.1002/ppul.25933
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Protein estimation in whole lung lavage fluid in hereditary pulmonary alveolar proteinosis due to a novel GM‐CSF receptor mutation.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1802, doi. 10.1002/ppul.25932
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Pediatric empyema: Are ultrasound characteristics at the time of intervention predictive of reintervention?
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1643, doi. 10.1002/ppul.25931
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RISK score for developing ventilator‐associated pneumonia in children: The RISVAP study.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1635, doi. 10.1002/ppul.25929
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Corticosteroid response predicts bronchopulmonary dysplasia status at 36 weeks in preterm infants treated with dexamethasone: A pilot study.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1760, doi. 10.1002/ppul.25928
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Transient low IgG4 levels cause recurrent wheezing requiring multiple hospitalizations in infancy.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1631, doi. 10.1002/ppul.25927
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Evaluation of the efficiency of the systemic immune‐inflammation index in differentiating parapneumonic effusion from empyema.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1625, doi. 10.1002/ppul.25926
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Evaluating FEV1 decline in diagnosis and management of pulmonary exacerbations in children with cystic fibrosis.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1709, doi. 10.1002/ppul.25925
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Low lymphocyte count: A clinical severity marker in infants with bronchiolitis.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1770, doi. 10.1002/ppul.25919
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Genetic diagnosis of immune dysregulation can lead to targeted therapy for interstitial lung disease: A case series and single center approach.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1577, doi. 10.1002/ppul.25924
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Spinal muscular atrophy: Surviving respiratory failure, intensive care and pursuing creatively fulfilled life.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1799, doi. 10.1002/ppul.25922
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Repeatability of lung clearance index in infants with cystic fibrosis and recurrent wheeze.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1608, doi. 10.1002/ppul.25921
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Serum homocysteine level in pediatric patients with COVID‐19 and its correlation with the disease severity.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1701, doi. 10.1002/ppul.25920
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Neonatal rodent ventilation and clinical correlation in congenital diaphragmatic hernia.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1600, doi. 10.1002/ppul.25911
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Oscillometry: A substitute of spirometry in children with neuromuscular diseases?
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1618, doi. 10.1002/ppul.25923
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Developing artificial intelligence technology for pediatric pulmonology: Lessons from COVID‐19.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1588, doi. 10.1002/ppul.25901
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Pilot study of nuclear scintigraphy to assess cough clearance in DMD.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1776, doi. 10.1002/ppul.25894
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Incidence, predictors of success and outcome of LISA in very preterm infants.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1751, doi. 10.1002/ppul.25798
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Issue Information.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1569, doi. 10.1002/ppul.25483
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- Article
Upcoming events of interest.
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- Pediatric Pulmonology, 2022, v. 57, n. 7, p. 1830, doi. 10.1002/ppul.25482
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- Article