Oded Breuer

Jerusalem, JM, Israel

Last Updated: 09/26/2026

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Found 58 publications

Management and Long-Term Outcomes of Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective Study.

Management and Long-Term Outcomes of Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective Study.

Journal: Chest

Published: October 11, 2025

Management and Long-Term Outcomes of Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective Study.

Management and Long-Term Outcomes of Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective Study.

Journal: Chest

Published: October 11, 2025

The Impact of Small-for-Gestational-Age on Pulmonary Function in Infancy, a Retrospective Cohort Study.

The Impact of Small-for-Gestational-Age on Pulmonary Function in Infancy, a Retrospective Cohort Study.

Journal: Pediatric pulmonology

Published: June 04, 2025

Recurrent Drug-induced Rhabdomyolysis in a 76-year-old Patient With Cystic Fibrosis: Drug-Drug Interactions in Older Patients With Cystic Fibrosis.

Recurrent Drug-induced Rhabdomyolysis in a 76-year-old Patient With Cystic Fibrosis: Drug-Drug Interactions in Older Patients With Cystic Fibrosis.

Journal: Clinical therapeutics

Published: May 28, 2025

Biallelic LAMP3 variants in 5 families with interstitial lung disease: Evidence of a disease-gene association.

Biallelic LAMP3 variants in 5 families with interstitial lung disease: Evidence of a disease-gene association.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 01, 2025

Long-term outcomes in people with CF lacking FEV1 response to elexacaftor/tezacaftor/ivacaftor therapy.

Long-term outcomes in people with CF lacking FEV1 response to elexacaftor/tezacaftor/ivacaftor therapy.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: March 18, 2025

Infant Pulmonary Function Testing in Pediatric Diffuse Parenchymal Lung Disease.

Infant Pulmonary Function Testing in Pediatric Diffuse Parenchymal Lung Disease.

Journal: CHEST pulmonary

Published: January 22, 2025

Nasal potential difference in young children is feasible - Report from a national referral center.

Nasal potential difference in young children is feasible - Report from a national referral center.

Journal: Respiratory medicine

Published: January 10, 2025

Bi-allelic LAMP3 variants in childhood interstitial lung disease: a surfactant-related disease.

Bi-allelic LAMP3 variants in childhood interstitial lung disease: a surfactant-related disease.

Journal: EBioMedicine

Published: November 08, 2024

Diagnostic Evaluation and Clinical Findings in Children With Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective Study.

Diagnostic Evaluation and Clinical Findings in Children With Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy: A European Multicenter Retrospective Study.

Journal: Chest

Published: October 08, 2024

Pulmonary function tests in infants following SARS-CoV-2 infection.

Pulmonary function tests in infants following SARS-CoV-2 infection.

Journal: Respiratory medicine

Published: June 09, 2024

Changes in Sleep in Children and Adults with Cystic Fibrosis and Primary Ciliary Dyskinesia over Time and after CFTR Modulator Therapy.

Changes in Sleep in Children and Adults with Cystic Fibrosis and Primary Ciliary Dyskinesia over Time and after CFTR Modulator Therapy.

Journal: Journal of clinical medicine

Published: November 04, 2023

Showing 1-12 of 58

Last Updated: 09/26/2026