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Marijke Proesmans

Showing results (91-100 of 118) with videos related to

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Frontiers in Immunology|May 30, 2017
Fifth Percentile Cutoff Values for Antipneumococcal Polysaccharide and Anti-<i>Salmonella typhi</i> Vi IgG Describe a Normal Polysaccharide ResponseHeidi Schaballie, Barbara Bosch, Rik Schrijvers, et al.
Hepatology (Baltimore, Md.)|March 5, 2011
Noncirrhotic presinusoidal portal hypertension is common in cystic fibrosis-associated liver diseasePeter Witters, Louis Libbrecht, Tania Roskams, et al.
Plos Pathogens|March 15, 2021
Genomics of an endemic cystic fibrosis Burkholderia multivorans strain reveals low within-patient evolution but high between-patient diversityCédric Lood, Charlotte Peeters, Quentin Lamy-Besnier, et al.
ERJ Open Research|February 27, 2024
ERS International Congress 2023: highlights from the Paediatrics AssemblySusanne J H Vijverberg, Asterios Kampouras, Halime Nayir Büyükşahin, et al.
ERJ Open Research|July 28, 2020
ERS International Congress, Madrid, 2019: highlights from the Paediatric AssemblyRaffaella Nenna, Monique Slaats, Refika Ersu, et al.
ERJ Open Research|May 25, 2023
ERS International Congress 2022: highlights from the Paediatrics AssemblyCristina Ardura-Garcia, Katharina Kainz, Maria Christina Mallet, et al.
ERJ Open Research|May 26, 2022
ERS International Congress 2021: highlights from the Paediatric AssemblyCristina Ardura-Garcia, Alicia Abellan, Sara Cuevas-Ocaña, et al.
Respiratory Medicine|May 12, 2026
Malnutrition in childhood interstitial lung diseases is associated with reduced lung function and greater disease severity: insights from the chILD-EU registryTugba Ramasli Gursoy, Nagehan Emiralioglu, Matthias Griese, 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.
The European Respiratory Journal|February 7, 2015
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patientsCarolin Kröner, Simone Reu, Veronika Teusch, et al.
Pageof 12

Showing results (91-100 of 118) with videos related to

Sort By:
Pageof 12
Frontiers in Immunology|May 30, 2017
Fifth Percentile Cutoff Values for Antipneumococcal Polysaccharide and Anti-<i>Salmonella typhi</i> Vi IgG Describe a Normal Polysaccharide ResponseHeidi Schaballie, Barbara Bosch, Rik Schrijvers, et al.
Hepatology (Baltimore, Md.)|March 5, 2011
Noncirrhotic presinusoidal portal hypertension is common in cystic fibrosis-associated liver diseasePeter Witters, Louis Libbrecht, Tania Roskams, et al.
Plos Pathogens|March 15, 2021
Genomics of an endemic cystic fibrosis Burkholderia multivorans strain reveals low within-patient evolution but high between-patient diversityCédric Lood, Charlotte Peeters, Quentin Lamy-Besnier, et al.
ERJ Open Research|February 27, 2024
ERS International Congress 2023: highlights from the Paediatrics AssemblySusanne J H Vijverberg, Asterios Kampouras, Halime Nayir Büyükşahin, et al.
ERJ Open Research|July 28, 2020
ERS International Congress, Madrid, 2019: highlights from the Paediatric AssemblyRaffaella Nenna, Monique Slaats, Refika Ersu, et al.
ERJ Open Research|May 25, 2023
ERS International Congress 2022: highlights from the Paediatrics AssemblyCristina Ardura-Garcia, Katharina Kainz, Maria Christina Mallet, et al.
ERJ Open Research|May 26, 2022
ERS International Congress 2021: highlights from the Paediatric AssemblyCristina Ardura-Garcia, Alicia Abellan, Sara Cuevas-Ocaña, et al.
Respiratory Medicine|May 12, 2026
Malnutrition in childhood interstitial lung diseases is associated with reduced lung function and greater disease severity: insights from the chILD-EU registryTugba Ramasli Gursoy, Nagehan Emiralioglu, Matthias Griese, 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.
The European Respiratory Journal|February 7, 2015
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patientsCarolin Kröner, Simone Reu, Veronika Teusch, et al.
Pageof 12