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Annals of the American Thoracic Society
|
November 7, 2022
Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype
Andrew T Barber, Adam J Shapiro, Stephanie D Davis, et al.
Annals of the American Thoracic Society
|
November 28, 2022
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype
BreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
The Journal of Pediatrics
|
February 8, 2025
Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta Syndrome
Adam J Shapiro, Eveline Y Wu, Deborah J Morris-Rosendahl, et al.
Thorax
|
December 21, 2011
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
Michael R Knowles, Margaret W Leigh, Johnny L Carson, et al.
American Journal of Human Genetics
|
December 25, 2012
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia
Michael R Knowles, Margaret W Leigh, Lawrence E Ostrowski, et al.
Annals of the American Thoracic Society
|
September 13, 2013
Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia
Margaret W Leigh, Milan J Hazucha, Kunal K Chawla, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 22, 2007
Diffuse lung disease in young children: application of a novel classification scheme
Gail H Deutsch, Lisa R Young, Robin R Deterding, et al.
ERJ Open Research
|
January 10, 2024
A BEAT-PCD consensus statement: a core outcome set for pulmonary disease interventions in primary ciliary dyskinesia
Renate Kos, Myrofora Goutaki, Helene E Kobbernagel, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 16, 2018
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline
Adam J Shapiro, Stephanie D Davis, Deepika Polineni, et al.
American Journal of Respiratory and Critical Care Medicine
|
February 27, 2014
Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype
Michael R Knowles, Lawrence E Ostrowski, Margaret W Leigh, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 105) with videos related to
Sort By:
Page
of 11
Annals of the American Thoracic Society
|
November 7, 2022
Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype
Andrew T Barber, Adam J Shapiro, Stephanie D Davis, et al.
Annals of the American Thoracic Society
|
November 28, 2022
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype
BreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
The Journal of Pediatrics
|
February 8, 2025
Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta Syndrome
Adam J Shapiro, Eveline Y Wu, Deborah J Morris-Rosendahl, et al.
Thorax
|
December 21, 2011
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
Michael R Knowles, Margaret W Leigh, Johnny L Carson, et al.
American Journal of Human Genetics
|
December 25, 2012
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia
Michael R Knowles, Margaret W Leigh, Lawrence E Ostrowski, et al.
Annals of the American Thoracic Society
|
September 13, 2013
Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia
Margaret W Leigh, Milan J Hazucha, Kunal K Chawla, et al.
American Journal of Respiratory and Critical Care Medicine
|
September 22, 2007
Diffuse lung disease in young children: application of a novel classification scheme
Gail H Deutsch, Lisa R Young, Robin R Deterding, et al.
ERJ Open Research
|
January 10, 2024
A BEAT-PCD consensus statement: a core outcome set for pulmonary disease interventions in primary ciliary dyskinesia
Renate Kos, Myrofora Goutaki, Helene E Kobbernagel, et al.
American Journal of Respiratory and Critical Care Medicine
|
June 16, 2018
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline
Adam J Shapiro, Stephanie D Davis, Deepika Polineni, et al.
American Journal of Respiratory and Critical Care Medicine
|
February 27, 2014
Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype
Michael R Knowles, Lawrence E Ostrowski, Margaret W Leigh, et al.
Page
of 11