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Oded Breuer

Showing results (41-50 of 50) with videos related to

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American Journal of Respiratory and Critical Care Medicine|February 28, 2019
Changing Prevalence of Lower Airway Infections in Young Children with Cystic FibrosisOded Breuer, Andre Schultz, Lidija Turkovic, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 23, 2017
Attention deficit hyperactivity disorder symptoms in patients with cystic fibrosisMalena Cohen-Cymberknoh, Tzlil Tanny, Oded Breuer, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 5, 2016
Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosisMalena Cohen-Cymberknoh, Noa Gilead, Silvia Gartner, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 18, 2023
Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutationIdo Sadras, Eitan Kerem, Galit Livnat, et al.
Respiratory Medicine|September 27, 2017
Clinical impact of Pseudomonas aeruginosa colonization in patients with Primary Ciliary DyskinesiaMalena Cohen-Cymberknoh, Nir Weigert, Alex Gileles-Hillel, et al.
Ebiomedicine|March 1, 2025
Bi-allelic LAMP3 variants in childhood interstitial lung disease: a surfactant-related diseaseCamille Louvrier, Tifenn Desroziers, Yohan Soreze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 7, 2026
Biallelic LAMP3 Variants in Five Families with Interstitial Lung Disease: Evidence of a Disease-Gene AssociationLaura A Keehan, Hitomi Ono-Minagi, Mohamad Hadhud, et al.
Plos Genetics|August 28, 2018
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertilityAsaf Ta-Shma, Rim Hjeij, Zeev Perles, et al.
Chest|February 13, 2026
Management and Long-Term Outcomes of Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective StudyHonorata Marczak, Katarzyna Krenke, Matthias Griese, et al.
Chest|March 7, 2025
Diagnostic Evaluation and Clinical Findings in Children With Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective StudyHonorata Marczak, Katarzyna Krenke, Matthias Griese, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
American Journal of Respiratory and Critical Care Medicine|February 28, 2019
Changing Prevalence of Lower Airway Infections in Young Children with Cystic FibrosisOded Breuer, Andre Schultz, Lidija Turkovic, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 23, 2017
Attention deficit hyperactivity disorder symptoms in patients with cystic fibrosisMalena Cohen-Cymberknoh, Tzlil Tanny, Oded Breuer, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 5, 2016
Eradication failure of newly acquired Pseudomonas aeruginosa isolates in cystic fibrosisMalena Cohen-Cymberknoh, Noa Gilead, Silvia Gartner, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 18, 2023
Clinical and functional efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis carrying the N1303K mutationIdo Sadras, Eitan Kerem, Galit Livnat, et al.
Respiratory Medicine|September 27, 2017
Clinical impact of Pseudomonas aeruginosa colonization in patients with Primary Ciliary DyskinesiaMalena Cohen-Cymberknoh, Nir Weigert, Alex Gileles-Hillel, et al.
Ebiomedicine|March 1, 2025
Bi-allelic LAMP3 variants in childhood interstitial lung disease: a surfactant-related diseaseCamille Louvrier, Tifenn Desroziers, Yohan Soreze, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 7, 2026
Biallelic LAMP3 Variants in Five Families with Interstitial Lung Disease: Evidence of a Disease-Gene AssociationLaura A Keehan, Hitomi Ono-Minagi, Mohamad Hadhud, et al.
Plos Genetics|August 28, 2018
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertilityAsaf Ta-Shma, Rim Hjeij, Zeev Perles, et al.
Chest|February 13, 2026
Management and Long-Term Outcomes of Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective StudyHonorata Marczak, Katarzyna Krenke, Matthias Griese, et al.
Chest|March 7, 2025
Diagnostic Evaluation and Clinical Findings in Children With Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective StudyHonorata Marczak, Katarzyna Krenke, Matthias Griese, et al.
Pageof 5