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W Leigh

Showing results (111-120 of 157) with videos related to

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Journal of Cell Science|February 18, 2022
The role of SPAG1 in the assembly of axonemal dyneins in human airway epitheliaAmanda J Smith, Ximena M Bustamante-Marin, Weining Yin, et al.
Pediatric Pulmonology|November 22, 2024
Therapies Used by Children With Primary Ciliary Dyskinesia: A Natural History StudyRobert A Gardner, Thomas W Ferkol, Stephanie D Davis, et al.
Pediatric Pulmonology|September 30, 2015
Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art reviewAdam J Shapiro, Maimoona A Zariwala, Thomas Ferkol, et al.
American Journal of Human Genetics|December 1, 2009
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defectsNiki Tomas Loges, Heike Olbrich, Anita Becker-Heck, et al.
OTO Open|February 24, 2025
Progression of Otologic and Nasal Symptoms in Primary Ciliary Dyskinesia Throughout ChildhoodIsabelle Dagher, Adam J Kimple, Thomas W Ferkol, et al.
Pediatric Pulmonology|February 2, 2011
Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: a multicenter experienceJ Tod Olin, Kim Burns, Johnny L Carson, et al.
Contemporary Clinical Trials Communications|February 28, 2023
Hybrid effectiveness-implementation trial of guided relaxation and acupuncture for chronic sickle cell disease pain (GRACE): A protocolArdith Z Doorenbos, Judith M Schlaeger, Victoria A deMartelly, 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.
Orphanet Journal of Rare Diseases|September 9, 2022
A multi-disciplinary, comprehensive approach to management of children with heterotaxyThomas G Saba, Gabrielle C Geddes, Stephanie M Ware, et al.
American Journal of Respiratory and Critical Care Medicine|August 2, 2018
Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and GenotypeStephanie D Davis, Margaret Rosenfeld, Hye-Seung Lee, et al.
Pageof 16

Showing results (111-120 of 157) with videos related to

Sort By:
Pageof 16
Journal of Cell Science|February 18, 2022
The role of SPAG1 in the assembly of axonemal dyneins in human airway epitheliaAmanda J Smith, Ximena M Bustamante-Marin, Weining Yin, et al.
Pediatric Pulmonology|November 22, 2024
Therapies Used by Children With Primary Ciliary Dyskinesia: A Natural History StudyRobert A Gardner, Thomas W Ferkol, Stephanie D Davis, et al.
Pediatric Pulmonology|September 30, 2015
Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art reviewAdam J Shapiro, Maimoona A Zariwala, Thomas Ferkol, et al.
American Journal of Human Genetics|December 1, 2009
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defectsNiki Tomas Loges, Heike Olbrich, Anita Becker-Heck, et al.
OTO Open|February 24, 2025
Progression of Otologic and Nasal Symptoms in Primary Ciliary Dyskinesia Throughout ChildhoodIsabelle Dagher, Adam J Kimple, Thomas W Ferkol, et al.
Pediatric Pulmonology|February 2, 2011
Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: a multicenter experienceJ Tod Olin, Kim Burns, Johnny L Carson, et al.
Contemporary Clinical Trials Communications|February 28, 2023
Hybrid effectiveness-implementation trial of guided relaxation and acupuncture for chronic sickle cell disease pain (GRACE): A protocolArdith Z Doorenbos, Judith M Schlaeger, Victoria A deMartelly, 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.
Orphanet Journal of Rare Diseases|September 9, 2022
A multi-disciplinary, comprehensive approach to management of children with heterotaxyThomas G Saba, Gabrielle C Geddes, Stephanie M Ware, et al.
American Journal of Respiratory and Critical Care Medicine|August 2, 2018
Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and GenotypeStephanie D Davis, Margaret Rosenfeld, Hye-Seung Lee, et al.
Pageof 16