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Peadar G Noone

Showing results (31-40 of 48) with videos related to

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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.
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.
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.
Chest|July 6, 2020
Airway Clearance Techniques in Bronchiectasis: Analysis From the United States Bronchiectasis and Non-TB Mycobacteria Research RegistryAshwin Basavaraj, Radmila Choate, Doreen Addrizzo-Harris, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 26, 2017
Frequency of untreated hypogammaglobulinemia in bronchiectasisMelanie A Ruffner, Timothy R Aksamit, Byron Thomashow, 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.
Thorax|December 19, 2015
US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summaryR Andres Floto, Kenneth N Olivier, Lisa Saiman, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|October 27, 2020
Nutrition and Markers of Disease Severity in Patients With BronchiectasisKatherine A Despotes, Radmila Choate, Doreen Addrizzo-Harris, et al.
American Journal of Respiratory and Critical Care Medicine|July 22, 2006
Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutationMaimoona A Zariwala, Margaret W Leigh, Franck Ceppa, et al.
Respiratory Medicine|January 5, 2021
Pseudomonas aeruginosa associated with severity of non-cystic fibrosis bronchiectasis measured by the modified bronchiectasis severity score (BSI) and the FACED: The US bronchiectasis and NTM Research Registry (BRR) studyRadmila Choate, Timothy R Aksamit, David Mannino, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
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.
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.
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.
Chest|July 6, 2020
Airway Clearance Techniques in Bronchiectasis: Analysis From the United States Bronchiectasis and Non-TB Mycobacteria Research RegistryAshwin Basavaraj, Radmila Choate, Doreen Addrizzo-Harris, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|May 26, 2017
Frequency of untreated hypogammaglobulinemia in bronchiectasisMelanie A Ruffner, Timothy R Aksamit, Byron Thomashow, 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.
Thorax|December 19, 2015
US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summaryR Andres Floto, Kenneth N Olivier, Lisa Saiman, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|October 27, 2020
Nutrition and Markers of Disease Severity in Patients With BronchiectasisKatherine A Despotes, Radmila Choate, Doreen Addrizzo-Harris, et al.
American Journal of Respiratory and Critical Care Medicine|July 22, 2006
Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutationMaimoona A Zariwala, Margaret W Leigh, Franck Ceppa, et al.
Respiratory Medicine|January 5, 2021
Pseudomonas aeruginosa associated with severity of non-cystic fibrosis bronchiectasis measured by the modified bronchiectasis severity score (BSI) and the FACED: The US bronchiectasis and NTM Research Registry (BRR) studyRadmila Choate, Timothy R Aksamit, David Mannino, et al.
Pageof 5