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Journal of Pediatric Gastroenterology and Nutrition
|
April 20, 2022
Changes in Glucose Breath Test in Cystic Fibrosis Patients Treated With 1 Month of Lumacaftor/Ivacaftor
Megan E Gabel, Hongyue Wang, Daniel Gelfond, et al.
JAMA Pediatrics
|
April 25, 2017
Effects of Diagnosis by Newborn Screening for Cystic Fibrosis on Weight and Length in the First Year of Life
Daniel H Leung, Sonya L Heltshe, Drucy Borowitz, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
November 28, 2017
Pancreatic Enzyme Replacement Therapy Use in Infants With Cystic Fibrosis Diagnosed by Newborn Screening
Daniel Gelfond, Sonya L Heltshe, Michelle Skalland, et al.
American Journal of Medical Genetics
|
September 20, 2002
Idiopathic congenital central hypoventilation syndrome: the next generation
Jean M Silvestri, Maida L Chen, Debra E Weese-Mayer, et al.
Journal of Medical Genetics
|
November 25, 2010
CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR
Molly B Sheridan, Timothy W Hefferon, Nulang Wang, et al.
Clinical and Translational Science
|
June 9, 2015
Standardization of Research-Quality Anthropometric Measurement of Infants and Implementation in a Multicenter Study
Christine Coburn-Miller, Susan Casey, Quynh Luong, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 25, 2023
Incidence of fibrosing colonopathy with pancreatic enzyme replacement therapy in patients with cystic fibrosis
Stephanie E Chiuve, Daniel Fife, Gerhard Leitz, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
June 27, 2018
RNA sequencing data from neutrophils of patients with cystic fibrosis reveals potential for developing biomarkers for pulmonary exacerbations
Kaiyu Jiang, Kerry E Poppenberg, Laiping Wong, et al.
Pediatric Pulmonology
|
January 24, 2019
Pulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort study
Danielle Goetz, Benjamin T Kopp, Ann Salvator, et al.
Annals of the American Thoracic Society
|
July 10, 2020
Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical Trial
Scott D Sagel, Umer Khan, Sonya L Heltshe, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 77) with videos related to
Sort By:
Page
of 8
Journal of Pediatric Gastroenterology and Nutrition
|
April 20, 2022
Changes in Glucose Breath Test in Cystic Fibrosis Patients Treated With 1 Month of Lumacaftor/Ivacaftor
Megan E Gabel, Hongyue Wang, Daniel Gelfond, et al.
JAMA Pediatrics
|
April 25, 2017
Effects of Diagnosis by Newborn Screening for Cystic Fibrosis on Weight and Length in the First Year of Life
Daniel H Leung, Sonya L Heltshe, Drucy Borowitz, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
November 28, 2017
Pancreatic Enzyme Replacement Therapy Use in Infants With Cystic Fibrosis Diagnosed by Newborn Screening
Daniel Gelfond, Sonya L Heltshe, Michelle Skalland, et al.
American Journal of Medical Genetics
|
September 20, 2002
Idiopathic congenital central hypoventilation syndrome: the next generation
Jean M Silvestri, Maida L Chen, Debra E Weese-Mayer, et al.
Journal of Medical Genetics
|
November 25, 2010
CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR
Molly B Sheridan, Timothy W Hefferon, Nulang Wang, et al.
Clinical and Translational Science
|
June 9, 2015
Standardization of Research-Quality Anthropometric Measurement of Infants and Implementation in a Multicenter Study
Christine Coburn-Miller, Susan Casey, Quynh Luong, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 25, 2023
Incidence of fibrosing colonopathy with pancreatic enzyme replacement therapy in patients with cystic fibrosis
Stephanie E Chiuve, Daniel Fife, Gerhard Leitz, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
June 27, 2018
RNA sequencing data from neutrophils of patients with cystic fibrosis reveals potential for developing biomarkers for pulmonary exacerbations
Kaiyu Jiang, Kerry E Poppenberg, Laiping Wong, et al.
Pediatric Pulmonology
|
January 24, 2019
Pulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort study
Danielle Goetz, Benjamin T Kopp, Ann Salvator, et al.
Annals of the American Thoracic Society
|
July 10, 2020
Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical Trial
Scott D Sagel, Umer Khan, Sonya L Heltshe, et al.
Page
of 8