Travaux scientifiques

Prof. Dr. Yasemin Gökdemir

311 publications. La source de l’information est indiquée à côté de chaque publication.

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  1. Long‐Term Effect Of COVID‐19 on Children's Lung Function: A Prospective Longitudinal Study

    Pediatric Pulmonology, 2026

    DOI 10.1002/ppul.71721 PMID 42376911 Source : OpenAlex

  2. Pulmonary Hypertension in Childhood Interstitial Lung Disease: Prevalence, Clinical Course, and Prognostic Impact from a National Registry

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa3985 Source : OpenAlex

  3. Current status of childhood interstitial lung disease in Turkiye: 5-year data from ChILD-TR

    BMJ Open Respiratory Research, 2026

    DOI 10.1136/bmjresp-2026-004626 PMID 42971729 Texte intégral en libre accèsSource : OpenAlex

  4. Advancements in Sweat Testing Techniques for Cystic Fibrosis: From Classical to Novel Methods

    Pediatric pulmonology, 2026

    DOI 10.1002/ppul.71573 PMID 41840955 Texte intégral en libre accèsSource : Europe PMC

  5. Evaluation of Pulmonary and Otological Manifestations in Primary Ciliary Dyskinesia and Their Effect on Quality of Life

    Pediatric pulmonology, 2026

    DOI 10.1002/ppul.71810 PMID 42643099 Texte intégral en libre accèsSource : Europe PMC

  6. Clinical Characteristics and Treatment Outcomes After First <i>Achromobacter</i> Isolation in Children with Cystic Fibrosis (Pre-CFTR Modulator Era)

    Thoracic research and practice, 2026

    DOI 10.4274/thoracrespract.2026.2026-1-8 PMID 42642966 Texte intégral en libre accèsSource : Europe PMC

  7. Evaluation of Pulmonary Complications in Patients with Esophageal Atresia

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa1733 Source : OpenAlex

  8. Isolated Hypoglycemia in Children with Cystic Fibrosis: Role of Pancreatic Insufficiency and Glucagon Response

    Journal of clinical research in pediatric endocrinology, 2026

    DOI 10.4274/jcrpe.galenos.2025.2025-2-6 PMID 41090401 Texte intégral en libre accèsSource : Europe PMC

  9. Bridging the Gap: Translated Medical Education to Support Cystic Fibrosis Centers From Non-English Speaking Countries

    Pediatric pulmonology, 2026

    DOI 10.1002/ppul.71764 PMID 42530427 1 citation (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  10. Interstitial Lung Disease in Children: Rare Genetic Variants Beyond Surfactant Dysfunction

    Pediatric pulmonology, 2026

    DOI 10.1002/ppul.71791 PMID 42598967 Texte intégral en libre accèsSource : Europe PMC

  11. Immunodeficiency-Associated Childhood Interstitial Lung Diseases: Data from the Türkiye chILD Registry

    Balkan medical journal, 2026

    DOI 10.4274/balkanmedj.galenos.2025.2025-10-42 PMID 41452243 Texte intégral en libre accèsSource : Europe PMC

  12. Pulmonary exacerbations in patients with genetically confirmed PCD: a prospective observational multicentre study

    Frontiers in Molecular Biosciences, 2026

    DOI 10.3389/fmolb.2026.1767533 PMID 42427487 4 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  13. Understanding Pulmonary Fibrosis in Pediatric Interstitial Lung Disease

    CHEST Journal, 2026

    DOI 10.1016/j.chest.2026.01.022 PMID 41740922 1 citation (OpenAlex) Source : OpenAlex

  14. Upper airway disease in PCD: Clinical management and factors influencing decision-making

    ERJ Open Research, 2026

    DOI 10.1183/23120541.00866-2026 Texte intégral en libre accèsSource : OpenAlex

  15. Frequency of liver involvement and its association with genotype in patients with cystic fibrosis

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa3954 Source : OpenAlex

  16. Long-term pulmonary function outcomes in patients with primary ciliary dyskinesia

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa1728 Source : OpenAlex

  17. Impact of CFTR Modulator Therapy on Muscle Strength in Pediatric Cystic Fibrosis Patients

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa3958 Source : OpenAlex

  18. Prolonged neonatal jaundice in infants with cystic fibrosis: a retrospective Cohort study

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa3960 Source : OpenAlex

  19. Utility of Video-Based Sleep Assessment in Identifying Obstructive Sleep Apnea in Pediatric Mucopolysaccharidoses

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa2811 Source : OpenAlex

  20. Clinical profile of people with primary ciliary dyskinesia during pulmonary exacerbations

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa2797 Source : OpenAlex

  21. Evaluation of lung function via spirometry and impulse oscillometry in preschool children with wheezing

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa2756 Source : OpenAlex

  22. Bone mineral density in children and adolescents with cystic fibrosis: a cross-sectional study

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa3947 Source : OpenAlex

  23. Vaccination Status and Attitudes in Patients with Cystic Fibrosis

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.oa2373 Source : OpenAlex

  24. Knowledge Level of Home Healthcare Personnel on Cystic Fibrosis: Evaluation Before and After Training

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa3949 Source : OpenAlex

  25. Do complex alleles matter? Real-world response to CFTR modulator therapy in cystic fibrosis

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa3952 Source : OpenAlex

  26. Association of upper airway symptoms with pulmonary exacerbations in people with primary ciliary dyskinesia

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.oa6602 Source : OpenAlex

  27. Upper airway disease management in patients with Primary Ciliary Dyskinesia (PCD): Insights from the EPIC-PCD study

    European Respiratory Journal, 2026

    DOI 10.1183/13993003.congress-2026.pa2799 Source : OpenAlex

  28. Effective Pseudomonas aeruginosa Eradication in Cystic Fibrosis: Multicenter Study

    Clinical Pediatrics, 2025

    DOI 10.1177/00099228251351699 PMID 40576045 1 citation (Europe PMC) Source : OpenAlex

  29. National Registry for Home Mechanical Ventilation in Children from Turkey

    Respiration, 2025

    DOI 10.1159/000543343 PMID 39809249 2 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  30. Eradication of Methicillin-Resistant Staphylococcus aureus in Cystic Fibrosis

    Clinical Pediatrics, 2025

    DOI 10.1177/00099228251375413 PMID 41035301 Source : OpenAlex

  31. The Importance of Bronchoalveolar Lavage Findings in Diagnosis and Their Relationship with Radiological Findings in Pediatric Interstitial Lung Diseases: Turkey chILD National Registry Cohort Study

    European Respiratory Journal, 2025

    DOI 10.1183/13993003.congress-2025.pa558 Source : OpenAlex

  32. Long‐Term Outcomes of Necrotizing Pneumonia and Parapneumonic Effusion in Children

    Pediatric Pulmonology, 2025

    DOI 10.1002/ppul.71241 PMID 40827719 6 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  33. Comparison of interrupted and continuous modulator therapy in cystic fibrosis: a real life experience in Turkey

    Frontiers in Pediatrics, 2025

    DOI 10.3389/fped.2025.1659633 PMID 41158800 1 citation (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

  34. Increasing Cystic Fibrosis Knowledge of Parents of Children Diagnosed With the Newborn Screening Program

    Pediatric Pulmonology, 2025

    DOI 10.1002/ppul.71392 PMID 41255258 Texte intégral en libre accèsSource : OpenAlex

  35. Personalized Management and Timing of Thymectomy in Juvenile Myasthenia Gravis: Insights from Routine Clinical Scale Use in a Single-Center Retrospective Cohort—A Case Series

    Children, 2025

    DOI 10.3390/children12101389 PMID 41153571 Texte intégral en libre accèsSource : OpenAlex

  36. The Coronal and Sagittal Vertebral Balance is Affected by the Severity of the Disease in Pediatric Patients with Cystic Fibrosis: A Pulmonary Function Test-Based Cross-Sectional Study

    Journal of Pediatric Orthopaedics, 2025

    DOI 10.1097/bpo.0000000000002947 PMID 40045563 Source : OpenAlex

  37. Feeding the Need: A Study on Food Security Among People With Cystic Fibrosis in Turkey

    Pediatric pulmonology, 2025

    DOI 10.1002/ppul.71101 PMID 40325925 1 citation (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  38. Elexacaftor/Tezacaftor/Ivacaftor Treatment Accessibility and Mental Health: Reducing Anxiety in People With Cystic Fibrosis

    Pediatric pulmonology, 2025

    DOI 10.1002/ppul.71037 PMID 40062574 5 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  39. Implementation of Cystic Fibrosis Responsibility, Independence, Self-Care, Education Program Enhances Cystic Fibrosis Knowledge in Limited Resource Country: Results From a Randomized Controlled Trial

    Pediatric pulmonology, 2025

    DOI 10.1002/ppul.27506 PMID 39898696 3 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  40. Pulmonary function in children post-empyema: spirometry <i>versus</i> lung clearance index

    ERJ open research, 2025

    DOI 10.1183/23120541.00855-2024 PMID 40874169 Texte intégral en libre accèsSource : Europe PMC

  41. Empowering limited-resource countries: collaborating with expert centers for diagnosis of primary ciliary dyskinesia

    Frontiers in Molecular Biosciences, 2025

    DOI 10.3389/fmolb.2025.1547152 PMID 40182617 5 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  42. Retrospective analysis of sleep-disordered breathing in pediatric neuromuscular disease

    Trends in Pediatrics, 2025

    DOI 10.59213/tp.2025.209 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  43. Clinical and demographic characteristics of patients diagnosed with Primary Ciliary Dyskinesia with CCDC40 homozygous mutation

    European Respiratory Journal, 2025

    DOI 10.1183/13993003.congress-2025.pa5919 Source : OpenAlex

  44. Cystic Fibrosis Treatment Landscape: Progress, Challenges, and Future Directions

    Turkish archives of pediatrics, 2025

    DOI 10.5152/turkarchpediatr.2025.24257 PMID 40091461 3 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

  45. The Validity and Reliability of the Turkish Version of the AWESCORE Test

    Turkish archives of pediatrics, 2025

    DOI 10.5152/turkarchpediatr.2025.24199 PMID 40091631 Texte intégral en libre accèsSource : Europe PMC

  46. First results from the international paediatric bronchiectasis registry (Child-BEAR-Net Registry) describing multicountry variations in childhood bronchiectasis and its management: a multicentre, cross-sectional study

    The Lancet Respiratory Medicine, 2025

    DOI 10.1016/s2213-2600(25)00089-x PMID 40757932 15 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  47. Microbial Contamination of Nebulizers in Patients With Cystic Fibrosis

    Turkish Archives of Pediatrics, 2025

    DOI 10.5152/turkarchpediatr.2025.24003 PMID 39803923 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  48. After the earthquake: Unmet needs in people with cystic fibrosis in Turkiye- multicenter study

    Journal of Cystic Fibrosis, 2025

    DOI 10.1016/j.jcf.2025.06.008 PMID 40675865 1 citation (OpenAlex) Source : OpenAlex

  49. A Hypomorphic Variant in Surfactant Protein B Deficiency : Survival of Two Patients

    Pediatric Pulmonology, 2025

    DOI 10.1002/ppul.71218 PMID 40709663 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

  50. Oral Health Status and Oral Health‐Related Quality of Life in Children With Primary Ciliary Dyskinesia

    Pediatric Pulmonology, 2025

    DOI 10.1002/ppul.71370 PMID 41221835 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex