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المؤلفون: Chiung Yu Huang, Meghan E. McGarry, Dennis W. Nielson, Ngoc P. Ly
المصدر: J Cyst Fibros
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, vol 20, iss 3مصطلحات موضوعية: Male, 0301 basic medicine, Pulmonary and Respiratory Medicine, medicine.medical_specialty, Longitudinal study, Younger age, Adolescent, Cystic Fibrosis, Clinical Sciences, Respiratory System, medicine.disease_cause, Cystic fibrosis, Article, Congenital, Young Adult, 03 medical and health sciences, Rare Diseases, 0302 clinical medicine, Clinical Research, Internal medicine, Humans, Medicine, Pseudomonas Infections, Longitudinal Studies, Registries, Preschool, Child, Lung, Survival analysis, Pediatric, Patient registry, business.industry, Pseudomonas aeruginosa, Hazard ratio, Infant, Newborn, Infant, Hispanic or Latino, Newborn, medicine.disease, United States, 030104 developmental biology, Increased risk, 030228 respiratory system, Child, Preschool, Pediatrics, Perinatology and Child Health, Health disparities, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::707afb2559bf0aa255d078a44c4d9628Test
https://doi.org/10.1016/j.jcf.2020.10.002Test -
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المؤلفون: Meghan E. McGarry, Ngoc P. Ly, John Neuhaus, Dennis W. Nielson
المصدر: Pediatr Pulmonol
Pediatric pulmonology, vol 54, iss 9مصطلحات موضوعية: Adult, Male, Pulmonary and Respiratory Medicine, Vital capacity, medicine.medical_specialty, Adolescent, Cystic Fibrosis, Respiratory System, Vital Capacity, Ethnic group, Cystic fibrosis, Article, White People, Pulmonary function testing, Paediatrics and Reproductive Medicine, Young Adult, 03 medical and health sciences, FEV1/FVC ratio, Rare Diseases, 0302 clinical medicine, Clinical Research, Forced Expiratory Volume, 030225 pediatrics, Epidemiology, medicine, Humans, Child, Lung, Retrospective Studies, pulmonary function testing, Patient registry, business.industry, Retrospective cohort study, Hispanic or Latino, respiratory system, medicine.disease, social dimensions of pulmonary medicine, United States, Respiratory Function Tests, Good Health and Well Being, 030228 respiratory system, Pediatrics, Perinatology and Child Health, Linear Models, epidemiology, Female, business, Demography
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd7e62a3f91bef08989af10ab86fcf13Test
https://doi.org/10.1002/ppul.24377Test -
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المصدر: Pediatric pulmonology, vol 52, iss 12
مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Adult, Male, Pediatrics, medicine.medical_specialty, Heterozygote, Adolescent, Cystic Fibrosis, hispanic latino, Respiratory System, Cystic Fibrosis Transmembrane Conductance Regulator, Cystic fibrosis, Article, Pulmonary function testing, Paediatrics and Reproductive Medicine, Cohort Studies, Congenital, 03 medical and health sciences, Young Adult, Rare Diseases, 0302 clinical medicine, Clinical Research, Forced Expiratory Volume, Epidemiology, medicine, Humans, 030212 general & internal medicine, Young adult, Child, Lung, pulmonary function testing, Patient registry, business.industry, Homozygote, Hispanic or Latino, medicine.disease, healthcare disparities, social dimensions of pulmonary medicine, Good Health and Well Being, medicine.anatomical_structure, 030228 respiratory system, Pediatrics, Perinatology and Child Health, Life expectancy, epidemiology, Female, business, Cohort study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a484ffe9f8991cc41a719044e3077acfTest
https://europepmc.org/articles/PMC5693693Test/ -
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المؤلفون: Meghan E. McGarry, Dennis W. Nielson, Beate Illek, Walter E. Finkbeiner, Lorna Zlock, Sabrina Olshansky, Courtney Moreno, Ngoc P. Ly
المصدر: Pediatric pulmonology, vol 52, iss 4
مصطلحات موضوعية: 0301 basic medicine, Male, Cystic Fibrosis, sweat chloride concentration, Respiratory System, Administration, Oral, Cystic Fibrosis Transmembrane Conductance Regulator, Quinolones, Aminophenols, Chloride, Cystic fibrosis, Pulmonary function testing, Ivacaftor, Congenital, 0302 clinical medicine, CFTR, Chloride Channel Agonists, Sweat, Lung, Cross-Over Studies, biology, integumentary system, personalized medicine, Middle Aged, Cystic fibrosis transmembrane conductance regulator, Treatment Outcome, Administration, Female, medicine.drug, Pulmonary and Respiratory Medicine, Oral, Adult, medicine.medical_specialty, Adolescent, Article, Paediatrics and Reproductive Medicine, 03 medical and health sciences, Young Adult, Rare Diseases, N-of-1 studies, Chlorides, In vivo, Clinical Research, Internal medicine, medicine, Humans, human nasal epithelium, Bronchiectasis, business.industry, Potentiator, medicine.disease, CFTR modulators, 030104 developmental biology, Endocrinology, 030228 respiratory system, Pediatrics, Perinatology and Child Health, biology.protein, ivacaftor, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a739de9d520cbbf525644276bf6aebe5Test
https://pubmed.ncbi.nlm.nih.gov/28068001Test