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G Noone

Showing results (61-70 of 84) with videos related to

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European Journal of Pediatrics|June 12, 2026
Ambulatory hypertension and left ventricular hypertrophy in pediatric chronic kidney disease: a systematic review and meta-analysisJason Chung, Andrew Yu, Cal Robinson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 10, 2000
Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosisP G Noone, K W Hohneker, Z Zhou, et al.
Pediatric Pulmonology|April 20, 2004
Standardized procedure for measurement of nasal potential difference: an outcome measure in multicenter cystic fibrosis clinical trialsThomas A Standaert, Louis Boitano, Julia Emerson, et al.
Kidney International|May 30, 2016
Von Willebrand factor regulates complement on endothelial cellsDamien G Noone, Magdalena Riedl, Fred G Pluthero, et al.
Circulation|May 23, 2007
Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesiaMarcus P Kennedy, Heymut Omran, Margaret W Leigh, et al.
Nature Genetics|January 15, 2002
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryHeike Olbrich, Karsten Häffner, Andreas Kispert, et al.
Pediatric Pulmonology|July 31, 2001
Safety of aerosolized INS 365 in patients with mild to moderate cystic fibrosis: results of a phase I multi-center studyP G Noone, N Hamblett, F Accurso, 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 defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.
Thorax|December 16, 2015
US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosisR Andres Floto, Kenneth N Olivier, Lisa Saiman, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|April 12, 2019
The Clinical Features of Bronchiectasis Associated with Alpha-1 Antitrypsin Deficiency, Common Variable Immunodeficiency and Primary Ciliary Dyskinesia--Results from the U.S. Bronchiectasis Research RegistryEdward Eden, Radmila Choate, Alan Barker, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
European Journal of Pediatrics|June 12, 2026
Ambulatory hypertension and left ventricular hypertrophy in pediatric chronic kidney disease: a systematic review and meta-analysisJason Chung, Andrew Yu, Cal Robinson, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 10, 2000
Safety and biological efficacy of a lipid-CFTR complex for gene transfer in the nasal epithelium of adult patients with cystic fibrosisP G Noone, K W Hohneker, Z Zhou, et al.
Pediatric Pulmonology|April 20, 2004
Standardized procedure for measurement of nasal potential difference: an outcome measure in multicenter cystic fibrosis clinical trialsThomas A Standaert, Louis Boitano, Julia Emerson, et al.
Kidney International|May 30, 2016
Von Willebrand factor regulates complement on endothelial cellsDamien G Noone, Magdalena Riedl, Fred G Pluthero, et al.
Circulation|May 23, 2007
Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesiaMarcus P Kennedy, Heymut Omran, Margaret W Leigh, et al.
Nature Genetics|January 15, 2002
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetryHeike Olbrich, Karsten Häffner, Andreas Kispert, et al.
Pediatric Pulmonology|July 31, 2001
Safety of aerosolized INS 365 in patients with mild to moderate cystic fibrosis: results of a phase I multi-center studyP G Noone, N Hamblett, F Accurso, 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 defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.
Thorax|December 16, 2015
US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosisR Andres Floto, Kenneth N Olivier, Lisa Saiman, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|April 12, 2019
The Clinical Features of Bronchiectasis Associated with Alpha-1 Antitrypsin Deficiency, Common Variable Immunodeficiency and Primary Ciliary Dyskinesia--Results from the U.S. Bronchiectasis Research RegistryEdward Eden, Radmila Choate, Alan Barker, et al.
Pageof 9