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Showing results (141-150 of 157) with videos related to

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Contemporary Clinical Trials|May 24, 2023
Equity and bias in electronic health records dataAndrew D Boyd, Rosa Gonzalez-Guarda, Katharine Lawrence, et al.
Cells|September 26, 2025
ODAD4-Related Primary Ciliary Dyskinesia: Report of Five Cases and a Founder Variant in QuebecMarie-Hélène Bourassa, Guillaume Sillon, Shuizi Ding, et al.
American Journal of Medical Genetics. Part A|October 4, 2024
Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary DyskinesiaM Makenzie Beaman, Weining Yin, Amanda J Smith, 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.
Journal of the American Medical Informatics Association : JAMIA|June 26, 2023
Potential bias and lack of generalizability in electronic health record data: reflections on health equity from the National Institutes of Health Pragmatic Trials CollaboratoryAndrew D Boyd, Rosa Gonzalez-Guarda, Katharine Lawrence, et al.
The European Respiratory Journal|December 23, 2017
Growth and nutritional status, and their association with lung function: a study from the international Primary Ciliary Dyskinesia CohortMyrofora Goutaki, Florian S Halbeisen, Ben D Spycher, et al.
American Journal of Human Genetics|July 16, 2013
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetryRim Hjeij, Anna Lindstrand, Richard Francis, et al.
The European Respiratory Journal|November 13, 2016
European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesiaJane S Lucas, Angelo Barbato, Samuel A Collins, et al.
American Journal of Human Genetics|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, 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 GuidelineAdam J Shapiro, Stephanie D Davis, Deepika Polineni, et al.
Pageof 16

Showing results (141-150 of 157) with videos related to

Sort By:
Pageof 16
Contemporary Clinical Trials|May 24, 2023
Equity and bias in electronic health records dataAndrew D Boyd, Rosa Gonzalez-Guarda, Katharine Lawrence, et al.
Cells|September 26, 2025
ODAD4-Related Primary Ciliary Dyskinesia: Report of Five Cases and a Founder Variant in QuebecMarie-Hélène Bourassa, Guillaume Sillon, Shuizi Ding, et al.
American Journal of Medical Genetics. Part A|October 4, 2024
Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary DyskinesiaM Makenzie Beaman, Weining Yin, Amanda J Smith, 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.
Journal of the American Medical Informatics Association : JAMIA|June 26, 2023
Potential bias and lack of generalizability in electronic health record data: reflections on health equity from the National Institutes of Health Pragmatic Trials CollaboratoryAndrew D Boyd, Rosa Gonzalez-Guarda, Katharine Lawrence, et al.
The European Respiratory Journal|December 23, 2017
Growth and nutritional status, and their association with lung function: a study from the international Primary Ciliary Dyskinesia CohortMyrofora Goutaki, Florian S Halbeisen, Ben D Spycher, et al.
American Journal of Human Genetics|July 16, 2013
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetryRim Hjeij, Anna Lindstrand, Richard Francis, et al.
The European Respiratory Journal|November 13, 2016
European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesiaJane S Lucas, Angelo Barbato, Samuel A Collins, et al.
American Journal of Human Genetics|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, 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 GuidelineAdam J Shapiro, Stephanie D Davis, Deepika Polineni, et al.
Pageof 16