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Adam J Shapiro

Showing results (51-60 of 73) with videos related to

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The Lancet. Respiratory Medicine|September 3, 2023
Safety and efficacy of the epithelial sodium channel blocker idrevloride in people with primary ciliary dyskinesia (CLEAN-PCD): a multinational, phase 2, randomised, double-blind, placebo-controlled crossover trialFelix C Ringshausen, Adam J Shapiro, Kim G Nielsen, et al.
Frontiers in Medicine|September 30, 2021
Novel <i>MYO1D</i> Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality DefectsRabab Said Alsafwani, Khalidah K Nasser, Thoraia Shinawi, et al.
American Journal of Human Genetics|October 31, 2025
Using the ancestral recombination graph to study the history of rare variants in founder populationsAlejandro Mejia-Garcia, Alex Diaz-Papkovich, Guillaume Sillon, 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.
Journal of Clinical Immunology|September 11, 2023
A Novel Homozygous Mutation Causing Complete TYK2 Deficiency, with Severe Respiratory Viral Infections, EBV-Driven Lymphoma, and Jamestown Canyon Viral EncephalitisLucie Roussel, Anne Pham-Huy, Andrea C Yu, 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.
Chest|March 1, 2014
Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxyAdam J Shapiro, Stephanie D Davis, Thomas Ferkol, 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.
Annals of the American Thoracic Society|October 9, 2024
Comparison of Longitudinal Outcomes in Children with Primary Ciliary Dyskinesia and Cystic FibrosisBreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
Chest|December 10, 2023
Situs Ambiguus Is Associated With Adverse Clinical Outcomes in Children With Primary Ciliary DyskinesiaKimberley R Kaspy, Sharon D Dell, Stephanie D Davis, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
The Lancet. Respiratory Medicine|September 3, 2023
Safety and efficacy of the epithelial sodium channel blocker idrevloride in people with primary ciliary dyskinesia (CLEAN-PCD): a multinational, phase 2, randomised, double-blind, placebo-controlled crossover trialFelix C Ringshausen, Adam J Shapiro, Kim G Nielsen, et al.
Frontiers in Medicine|September 30, 2021
Novel <i>MYO1D</i> Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality DefectsRabab Said Alsafwani, Khalidah K Nasser, Thoraia Shinawi, et al.
American Journal of Human Genetics|October 31, 2025
Using the ancestral recombination graph to study the history of rare variants in founder populationsAlejandro Mejia-Garcia, Alex Diaz-Papkovich, Guillaume Sillon, 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.
Journal of Clinical Immunology|September 11, 2023
A Novel Homozygous Mutation Causing Complete TYK2 Deficiency, with Severe Respiratory Viral Infections, EBV-Driven Lymphoma, and Jamestown Canyon Viral EncephalitisLucie Roussel, Anne Pham-Huy, Andrea C Yu, 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.
Chest|March 1, 2014
Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxyAdam J Shapiro, Stephanie D Davis, Thomas Ferkol, 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.
Annals of the American Thoracic Society|October 9, 2024
Comparison of Longitudinal Outcomes in Children with Primary Ciliary Dyskinesia and Cystic FibrosisBreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
Chest|December 10, 2023
Situs Ambiguus Is Associated With Adverse Clinical Outcomes in Children With Primary Ciliary DyskinesiaKimberley R Kaspy, Sharon D Dell, Stephanie D Davis, et al.
Pageof 8