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The Journal of Allergy and Clinical Immunology
|
December 3, 2014
Vitamin D enhances production of soluble ST2, inhibiting the action of IL-33
Paul E Pfeffer, Yin-Huai Chen, Grzegorz Woszczek, et al.
American Journal of Respiratory Cell and Molecular Biology
|
February 2, 2008
Nasal abnormalities in cystic fibrosis mice independent of infection and inflammation
Tom N Hilliard, Jie Zhu, Ray Farley, et al.
Chest
|
January 12, 2008
Endobronchial biopsy in childhood
Nicolas Regamey, Tom N Hilliard, Sejal Saglani, et al.
Pediatric Pulmonology
|
April 23, 2014
Mannose-binding lectin 2 gene polymorphism and lung damage in primary ciliary dyskinesia
Massimo Pifferi, Andrew Bush, Angela Michelucci, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 26, 2008
Increased airway smooth muscle mass in children with asthma, cystic fibrosis, and non-cystic fibrosis bronchiectasis
Nicolas Regamey, Matthias Ochs, Tom N Hilliard, et al.
Diagnostics (Basel, Switzerland)
|
December 23, 2022
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective
Spyros A Papiris, Caroline Kannengiesser, Raphael Borie, et al.
Pediatric Pulmonology
|
January 3, 2024
The genetic framework of primary ciliary dyskinesia assessed by soft computing analysis
Massimo Pifferi, Attilio L Boner, Angela Cangiotti, et al.
Thorax
|
March 2, 2018
Olfactory dysfunction is worse in primary ciliary dyskinesia compared with other causes of chronic sinusitis in children
Massimo Pifferi, Andrew Bush, Michele Rizzo, et al.
Thorax
|
July 3, 2015
European protocols for the diagnosis and initial treatment of interstitial lung disease in children
Andrew Bush, Steve Cunningham, Jacques de Blic, et al.
American Journal of Respiratory and Critical Care Medicine
|
February 3, 2004
The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis
Sarath C Ranganathan, Janet Stocks, Carol Dezateux, et al.
Page
of 67
Search research articles
Search
Showing results (551-560 of 670) with videos related to
Sort By:
Page
of 67
The Journal of Allergy and Clinical Immunology
|
December 3, 2014
Vitamin D enhances production of soluble ST2, inhibiting the action of IL-33
Paul E Pfeffer, Yin-Huai Chen, Grzegorz Woszczek, et al.
American Journal of Respiratory Cell and Molecular Biology
|
February 2, 2008
Nasal abnormalities in cystic fibrosis mice independent of infection and inflammation
Tom N Hilliard, Jie Zhu, Ray Farley, et al.
Chest
|
January 12, 2008
Endobronchial biopsy in childhood
Nicolas Regamey, Tom N Hilliard, Sejal Saglani, et al.
Pediatric Pulmonology
|
April 23, 2014
Mannose-binding lectin 2 gene polymorphism and lung damage in primary ciliary dyskinesia
Massimo Pifferi, Andrew Bush, Angela Michelucci, et al.
American Journal of Respiratory and Critical Care Medicine
|
January 26, 2008
Increased airway smooth muscle mass in children with asthma, cystic fibrosis, and non-cystic fibrosis bronchiectasis
Nicolas Regamey, Matthias Ochs, Tom N Hilliard, et al.
Diagnostics (Basel, Switzerland)
|
December 23, 2022
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective
Spyros A Papiris, Caroline Kannengiesser, Raphael Borie, et al.
Pediatric Pulmonology
|
January 3, 2024
The genetic framework of primary ciliary dyskinesia assessed by soft computing analysis
Massimo Pifferi, Attilio L Boner, Angela Cangiotti, et al.
Thorax
|
March 2, 2018
Olfactory dysfunction is worse in primary ciliary dyskinesia compared with other causes of chronic sinusitis in children
Massimo Pifferi, Andrew Bush, Michele Rizzo, et al.
Thorax
|
July 3, 2015
European protocols for the diagnosis and initial treatment of interstitial lung disease in children
Andrew Bush, Steve Cunningham, Jacques de Blic, et al.
American Journal of Respiratory and Critical Care Medicine
|
February 3, 2004
The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis
Sarath C Ranganathan, Janet Stocks, Carol Dezateux, et al.
Page
of 67