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American Journal of Respiratory and Critical Care Medicine
|
August 2, 2018
Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype
Stephanie D Davis, Margaret Rosenfeld, Hye-Seung Lee, et al.
Diabetes
|
May 15, 2013
Genetic modifiers of cystic fibrosis-related diabetes
Scott M Blackman, Clayton W Commander, Christopher Watson, et al.
Journal of Clinical Psychology in Medical Settings
|
September 24, 2021
Extending the Common Sense Model to Explore the Impact of the Fear of COVID-19 on Quality of Life in an International Inflammatory Bowel Disease Cohort
Bree Hayes, Pragalathan Apputhurai, Antonina Mikocka-Walus, et al.
The Journal of Pediatrics
|
March 16, 2015
Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis
Melissa R Miller, David Soave, Weili Li, et al.
Annals of the American Thoracic Society
|
October 9, 2024
Comparison of Longitudinal Outcomes in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis
BreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
American Journal of Respiratory and Critical Care Medicine
|
April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects
Nada Hornef, Heike Olbrich, Judit Horvath, et al.
Physiological Genomics
|
December 24, 2009
EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity
Rebecca Darrah, Edward McKone, Clare O'Connor, et al.
Chest
|
December 10, 2023
Situs Ambiguus Is Associated With Adverse Clinical Outcomes in Children With Primary Ciliary Dyskinesia
Kimberley R Kaspy, Sharon D Dell, Stephanie D Davis, et al.
American Journal of Respiratory and Critical Care Medicine
|
December 11, 2014
Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype
Stephanie D Davis, Thomas W Ferkol, Margaret Rosenfeld, et al.
Pediatric Pulmonology
|
May 9, 2025
The Association of Neonatal Respiratory Distress With Ciliary Ultrastructure and Genotype in Primary Ciliary Dyskinesia
Andrew T Barber, Stephanie D Davis, Thomas W Ferkol, et al.
Page
of 95
Search research articles
Search
Showing results (881-890 of 950) with videos related to
Sort By:
Page
of 95
American Journal of Respiratory and Critical Care Medicine
|
August 2, 2018
Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype
Stephanie D Davis, Margaret Rosenfeld, Hye-Seung Lee, et al.
Diabetes
|
May 15, 2013
Genetic modifiers of cystic fibrosis-related diabetes
Scott M Blackman, Clayton W Commander, Christopher Watson, et al.
Journal of Clinical Psychology in Medical Settings
|
September 24, 2021
Extending the Common Sense Model to Explore the Impact of the Fear of COVID-19 on Quality of Life in an International Inflammatory Bowel Disease Cohort
Bree Hayes, Pragalathan Apputhurai, Antonina Mikocka-Walus, et al.
The Journal of Pediatrics
|
March 16, 2015
Variants in Solute Carrier SLC26A9 Modify Prenatal Exocrine Pancreatic Damage in Cystic Fibrosis
Melissa R Miller, David Soave, Weili Li, et al.
Annals of the American Thoracic Society
|
October 9, 2024
Comparison of Longitudinal Outcomes in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis
BreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
American Journal of Respiratory and Critical Care Medicine
|
April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects
Nada Hornef, Heike Olbrich, Judit Horvath, et al.
Physiological Genomics
|
December 24, 2009
EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severity
Rebecca Darrah, Edward McKone, Clare O'Connor, et al.
Chest
|
December 10, 2023
Situs Ambiguus Is Associated With Adverse Clinical Outcomes in Children With Primary Ciliary Dyskinesia
Kimberley R Kaspy, Sharon D Dell, Stephanie D Davis, et al.
American Journal of Respiratory and Critical Care Medicine
|
December 11, 2014
Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype
Stephanie D Davis, Thomas W Ferkol, Margaret Rosenfeld, et al.
Pediatric Pulmonology
|
May 9, 2025
The Association of Neonatal Respiratory Distress With Ciliary Ultrastructure and Genotype in Primary Ciliary Dyskinesia
Andrew T Barber, Stephanie D Davis, Thomas W Ferkol, et al.
Page
of 95