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Francesca Santamaria

Showing results (101-110 of 121) with videos related to

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Med (New York, N.Y.)|November 15, 2024
Multi-year enzyme expression in patients with mucopolysaccharidosis type VI after liver-directed gene therapyAlessandro Rossi, Roberta Romano, Simona Fecarotta, et al.
The European Respiratory Journal|December 15, 2015
An international registry for primary ciliary dyskinesiaClaudius Werner, Martin Lablans, Maximilian Ataian, et al.
Italian Journal of Pediatrics|March 6, 2019
Consensus communication strategies to improve doctor-patient relationship in paediatric severe asthmaAntonietta Cappuccio, , Filomena Bugliaro, et al.
Pediatric Pulmonology|January 1, 2023
Primary ciliary dyskinesia: A multicenter survey on clinical practice and patient management in ItalyNicola Ullmann, Francesca Santamaria, Annalisa Allegorico, et al.
American Journal of Human Genetics|May 5, 2018
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein ArmsInga M Höben, Rim Hjeij, Heike Olbrich, et al.
ERJ Open Research|September 23, 2020
Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesiaSuzanne Crowley, Inês Azevedo, Mieke Boon, et al.
The European Respiratory Journal|July 28, 2018
Lung function in patients with primary ciliary dyskinesia: an iPCD Cohort studyFlorian S Halbeisen, Myrofora Goutaki, Ben D Spycher, et al.
The European Respiratory Journal|March 18, 2022
Lung function from school age to adulthood in primary ciliary dyskinesiaFlorian S Halbeisen, Eva S L Pedersen, Myrofora Goutaki, 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.
Frontiers in Molecular Biosciences|July 10, 2026
Pulmonary exacerbations in patients with genetically confirmed PCD: a prospective observational multicentre studyPinelopi Anagnostopoulou, Panayiotis Kouis, Dilber Ademhan Tural, et al.
Pageof 13

Showing results (101-110 of 121) with videos related to

Sort By:
Pageof 13
Med (New York, N.Y.)|November 15, 2024
Multi-year enzyme expression in patients with mucopolysaccharidosis type VI after liver-directed gene therapyAlessandro Rossi, Roberta Romano, Simona Fecarotta, et al.
The European Respiratory Journal|December 15, 2015
An international registry for primary ciliary dyskinesiaClaudius Werner, Martin Lablans, Maximilian Ataian, et al.
Italian Journal of Pediatrics|March 6, 2019
Consensus communication strategies to improve doctor-patient relationship in paediatric severe asthmaAntonietta Cappuccio, , Filomena Bugliaro, et al.
Pediatric Pulmonology|January 1, 2023
Primary ciliary dyskinesia: A multicenter survey on clinical practice and patient management in ItalyNicola Ullmann, Francesca Santamaria, Annalisa Allegorico, et al.
American Journal of Human Genetics|May 5, 2018
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein ArmsInga M Höben, Rim Hjeij, Heike Olbrich, et al.
ERJ Open Research|September 23, 2020
Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesiaSuzanne Crowley, Inês Azevedo, Mieke Boon, et al.
The European Respiratory Journal|July 28, 2018
Lung function in patients with primary ciliary dyskinesia: an iPCD Cohort studyFlorian S Halbeisen, Myrofora Goutaki, Ben D Spycher, et al.
The European Respiratory Journal|March 18, 2022
Lung function from school age to adulthood in primary ciliary dyskinesiaFlorian S Halbeisen, Eva S L Pedersen, Myrofora Goutaki, 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.
Frontiers in Molecular Biosciences|July 10, 2026
Pulmonary exacerbations in patients with genetically confirmed PCD: a prospective observational multicentre studyPinelopi Anagnostopoulou, Panayiotis Kouis, Dilber Ademhan Tural, et al.
Pageof 13