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Archives of Disease in Childhood. Education and Practice Edition
|
December 6, 2013
Pulse oximetry in children
Ian P Sinha, Sarah J Mayell, Clare Halfhide
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 8, 2010
Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening
Isabelle Sermet-Gaudelus, Sarah J Mayell, Kevin W Southern, et al.
The Lancet. Respiratory Medicine
|
December 26, 2021
Eat or heat: fuel poverty and childhood respiratory health
Cassandra Barrett, Alice R Lee, Elissa M Abrams, et al.
Respiratory Medicine and Research
|
April 12, 2026
Chalazion and hordeolum associated with Elexacaftor-Tezacaftor-Ivacaftor use in children with cystic fibrosis
Christy Liew, Andrew Brookes, Emma L Guy, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
February 27, 2021
Defining key outcomes to evaluate performance of newborn screening programmes for cystic fibrosis
Anne Munck, Kevin W Southern, Carlo Castellani, et al.
The Lancet. Respiratory Medicine
|
July 3, 2020
Child poverty, food insecurity, and respiratory health during the COVID-19 pandemic
Ian P Sinha, Alice R Lee, Davara Bennett, et al.
Pediatric Pulmonology
|
August 8, 2020
Persistent tachypnea of infancy: Follow up at school age
Elias Seidl, Julia Carlens, Nicolaus Schwerk, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 1, 2020
Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID)
Jürg Barben, Carlo Castellani, Anne Munck, et al.
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Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Archives of Disease in Childhood. Education and Practice Edition
|
December 6, 2013
Pulse oximetry in children
Ian P Sinha, Sarah J Mayell, Clare Halfhide
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 8, 2010
Guidelines on the early management of infants diagnosed with cystic fibrosis following newborn screening
Isabelle Sermet-Gaudelus, Sarah J Mayell, Kevin W Southern, et al.
The Lancet. Respiratory Medicine
|
December 26, 2021
Eat or heat: fuel poverty and childhood respiratory health
Cassandra Barrett, Alice R Lee, Elissa M Abrams, et al.
Respiratory Medicine and Research
|
April 12, 2026
Chalazion and hordeolum associated with Elexacaftor-Tezacaftor-Ivacaftor use in children with cystic fibrosis
Christy Liew, Andrew Brookes, Emma L Guy, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
February 27, 2021
Defining key outcomes to evaluate performance of newborn screening programmes for cystic fibrosis
Anne Munck, Kevin W Southern, Carlo Castellani, et al.
The Lancet. Respiratory Medicine
|
July 3, 2020
Child poverty, food insecurity, and respiratory health during the COVID-19 pandemic
Ian P Sinha, Alice R Lee, Davara Bennett, et al.
Pediatric Pulmonology
|
August 8, 2020
Persistent tachypnea of infancy: Follow up at school age
Elias Seidl, Julia Carlens, Nicolaus Schwerk, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 1, 2020
Updated guidance on the management of children with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome/cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID)
Jürg Barben, Carlo Castellani, Anne Munck, et al.
Page
of 1