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Stephanie D Davis

Showing results (161-170 of 167) with videos related to

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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.
Annals of the American Thoracic Society|April 24, 2013
An official American Thoracic Society workshop report: optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of ageMargaret Rosenfeld, Julian Allen, Bert H G M Arets, et al.
American Journal of Respiratory and Critical Care Medicine|June 5, 2007
An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool childrenNicole Beydon, Stephanie D Davis, Enrico Lombardi, 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 phenotypeMichael R Knowles, Lawrence E Ostrowski, Margaret W Leigh, et al.
American Journal of Human Genetics|September 24, 2013
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein armsMichael R Knowles, Lawrence E Ostrowski, Niki T Loges, et al.
American Journal of Human Genetics|October 8, 2013
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary DyskinesiaChristina Austin-Tse, Jan Halbritter, Maimoona A Zariwala, et al.
Pageof 17

Showing results (161-170 of 167) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 167 results.
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.
Annals of the American Thoracic Society|April 24, 2013
An official American Thoracic Society workshop report: optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of ageMargaret Rosenfeld, Julian Allen, Bert H G M Arets, et al.
American Journal of Respiratory and Critical Care Medicine|June 5, 2007
An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool childrenNicole Beydon, Stephanie D Davis, Enrico Lombardi, 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 phenotypeMichael R Knowles, Lawrence E Ostrowski, Margaret W Leigh, et al.
American Journal of Human Genetics|September 24, 2013
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein armsMichael R Knowles, Lawrence E Ostrowski, Niki T Loges, et al.
American Journal of Human Genetics|October 8, 2013
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary DyskinesiaChristina Austin-Tse, Jan Halbritter, Maimoona A Zariwala, et al.
Pageof 17