Works matching IS 87556863 AND DT 2024 AND VI 59 AND IP 3
Results: 42
Decoding negative genetic panels in primary ciliary dyskinesia.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 784, doi. 10.1002/ppul.26790
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- Article
Upcoming events of interest.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 816, doi. 10.1002/ppul.26902
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- Article
An 8‐year‐old boy with Scimitar syndrome: Presentation with gastroesophageal reflux symptoms and concurrent associations, including ectopic herniated liver.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 779, doi. 10.1002/ppul.26808
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Breastfeeding in infants who aspirate may increase risk of pulmonary inflammation.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 600, doi. 10.1002/ppul.26788
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Lung ultrasound evaluation in people with cystic fibrosis: A new approach in the pulmonology outpatient clinic.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 592, doi. 10.1002/ppul.26787
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Respiratory function testing for guiding ventilator mode conversion in congenital diaphragmatic hernia.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 609, doi. 10.1002/ppul.26789
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Calculating intrinsic positive end‐expiratory pressure from end‐expiratory flow in mechanically ventilated children—A study in physical models of the pediatric respiratory system.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 766, doi. 10.1002/ppul.26828
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Lung ultrasound: A potential tool in the diagnosis of ventilator‐associated pneumonia in pediatric intensive care units.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 758, doi. 10.1002/ppul.26827
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Analgosedation for less‐invasive surfactant administration: Variations in practice.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 750, doi. 10.1002/ppul.26826
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Asthma care: The need for evidence‐based, equitable, and affordable approaches.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 798, doi. 10.1002/ppul.26825
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Palivizumab prophylaxis in preterm infants and subsequent wheezing/asthma: 10‐year follow‐up study.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 743, doi. 10.1002/ppul.26824
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Impact of elexacaftor/tezacaftor/ivacaftor on lipid and fat‐soluble vitamin levels and association with body mass index.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 734, doi. 10.1002/ppul.26823
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Sore throat as the herald of spontaneous pneumomediastinum.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 782, doi. 10.1002/ppul.26822
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Pediatric systemic juvenile idiopathic arthritis‐related lung disease: Description of clinical cohort and review of management.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 724, doi. 10.1002/ppul.26821
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Assessing the economic implications of impulse oscillometry in preschoolers with asthma in Colombia.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 813, doi. 10.1002/ppul.26820
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Flexible bronchoscopy findings and management impact in children with oropharyngeal dysphagia.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 715, doi. 10.1002/ppul.26819
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The impact of maternal hyperemesis gravidarum on early childhood respiratory morbidity.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 707, doi. 10.1002/ppul.26817
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The airway microbiota in siblings with primary ciliary dyskinesia: Related factors and correlation with clinical characteristics.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 695, doi. 10.1002/ppul.26816
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Pulmonary manifestations of STAC3 disorder: A case series.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 794, doi. 10.1002/ppul.26815
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Pulmonary functions, nasal symptoms, and quality of life in patients with primary ciliary dyskinesia (PCD).
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 688, doi. 10.1002/ppul.26814
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Associations between symptoms of ADHD/ODD and health outcomes in youth with cystic fibrosis.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 809, doi. 10.1002/ppul.26811
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Infants hospitalized with lower respiratory tract infections during the first two years of life have increased risk of pediatric obstructive sleep apnea.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 679, doi. 10.1002/ppul.26810
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Cystic fibrosis transmembrane conductance regulator modulator administration to a F508del heterozygous infant with meconium pseudocyst and short bowel syndrome: A case report.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 791, doi. 10.1002/ppul.26809
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The hidden highway: A forgotten complication of oropharyngeal infection in children.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 776, doi. 10.1002/ppul.26807
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Analysis of iron status after initiation of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 669, doi. 10.1002/ppul.26805
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Lung ultrasound scores within the first 3 days of life to predict respiratory outcomes.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 662, doi. 10.1002/ppul.26804
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A decade of change: The evolution of pharmacy services at U.S. cystic fibrosis centers.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 652, doi. 10.1002/ppul.26798
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Venous thromboembolism management in people with cystic fibrosis.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 584, doi. 10.1002/ppul.26786
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Body composition in children with cystic fibrosis treated with CFTR modulators versus modulator naïve individuals.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 805, doi. 10.1002/ppul.26797
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Pediatric long‐term noninvasive respiratory support in children with central nervous system disorders.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 642, doi. 10.1002/ppul.26796
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Bronchopulmonary dysplasia in adults: Exploring pathogenesis and phenotype.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 540, doi. 10.1002/ppul.26795
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Elexacaftor/tezacaftor/ivacaftor can rescue pancreatic function in F508del homozygous children.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 788, doi. 10.1002/ppul.26794
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Bronchiolitis hospital admission in infancy is associated with later preschool ventilation inhomogeneity.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 632, doi. 10.1002/ppul.26793
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Bronchoscopic treatment of pediatric atelectasis: A modified segmental insufflation‐surfactant instillation technique.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 625, doi. 10.1002/ppul.26792
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- Article
Spontaneous breathing in selected neonates with very mild congenital diaphragmatic hernia.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 617, doi. 10.1002/ppul.26791
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A comparative analysis of the Vasoactive‐Inotropic Score, the Vasoactive‐Ventilation‐Renal Score, and the Oxygenation Index as outcome predictors in infants with a congenital diaphragmatic hernia.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 574, doi. 10.1002/ppul.26785
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Ganglioneuroma presents as the absence of sweating on the face and the opposite trunk in a child.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 774, doi. 10.1002/ppul.26784
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The effects of inspiratory muscle training on cardiorespiratory functions in juvenile idiopathic arthritis: A randomized controlled trial.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 562, doi. 10.1002/ppul.26783
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Combining biologics and CFTR modulators is safe: A pilot, observational, monocenter study.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 801, doi. 10.1002/ppul.26782
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Home‐spirometry exacerbation profiles in children with cystic fibrosis.
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 552, doi. 10.1002/ppul.26781
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Neuropsychiatric symptoms with elexacaftor/tezacaftor/ivacaftor: What does this mean for children?
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- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 537, doi. 10.1002/ppul.26762
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Issue Information.
- Published in:
- Pediatric Pulmonology, 2024, v. 59, n. 3, p. 529, doi. 10.1002/ppul.26505
- Publication type:
- Article