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Marijke Proesmans

Showing results (81-90 of 118) with videos related to

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The European Respiratory Journal|August 5, 2020
Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosisAnabela S Ramalho, Eva Fürstová, Annelotte M Vonk, et al.
Journal of Clinical Immunology|January 19, 2020
Systemic Inflammation and Myelofibrosis in a Patient with Takenouchi-Kosaki Syndrome due to CDC42 Tyr64Cys MutationGiorgia Bucciol, Bethany Pillay, Jose Casas-Martin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 13, 2022
European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performanceAnne Munck, Daria O Berger, Kevin W Southern, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 29, 2025
Correlation between patient-derived intestinal organoids and clinical responses to CFTR modulators in people with cystic fibrosis homozygous for F508delNoelia Rodriguez Mier, Senne Cuyx, Kris De Boeck, et al.
American Journal of Respiratory and Critical Care Medicine|October 17, 2015
Persistent Tachypnea of Infancy. Usual and AberrantDaniela Rauch, Martin Wetzke, Simone Reu, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|July 24, 2020
Pulmonary function testing in children's interstitial lung diseaseAstrid Madsen Ring, Julia Carlens, Andy Bush, et al.
Journal of Clinical Immunology|November 10, 2019
Defining Polysaccharide Antibody Deficiency: Measurement of Anti-Pneumococcal Antibodies and Anti-Salmonella typhi Antibodies in a Cohort of Patients with Recurrent InfectionsGiorgia Bucciol, Heidi Schaballie, Rik Schrijvers, et al.
Clinical Genetics|June 24, 2021
Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancyChristina K Rapp, Ine Van Dijck, Lucia Laugwitz, et al.
Thorax|February 12, 2022
Acute exacerbations in children's interstitial lung diseaseElias Seidl, Nicolaus Schwerk, Julia Carlens, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2022
Severity of the S1251N allele in cystic fibrosis is affected by the presence of the F508C variant in cisSenne Cuyx, Sofia S Ramalho, Isabelle Callebaut, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
The European Respiratory Journal|August 5, 2020
Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosisAnabela S Ramalho, Eva Fürstová, Annelotte M Vonk, et al.
Journal of Clinical Immunology|January 19, 2020
Systemic Inflammation and Myelofibrosis in a Patient with Takenouchi-Kosaki Syndrome due to CDC42 Tyr64Cys MutationGiorgia Bucciol, Bethany Pillay, Jose Casas-Martin, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 13, 2022
European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performanceAnne Munck, Daria O Berger, Kevin W Southern, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 29, 2025
Correlation between patient-derived intestinal organoids and clinical responses to CFTR modulators in people with cystic fibrosis homozygous for F508delNoelia Rodriguez Mier, Senne Cuyx, Kris De Boeck, et al.
American Journal of Respiratory and Critical Care Medicine|October 17, 2015
Persistent Tachypnea of Infancy. Usual and AberrantDaniela Rauch, Martin Wetzke, Simone Reu, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|July 24, 2020
Pulmonary function testing in children's interstitial lung diseaseAstrid Madsen Ring, Julia Carlens, Andy Bush, et al.
Journal of Clinical Immunology|November 10, 2019
Defining Polysaccharide Antibody Deficiency: Measurement of Anti-Pneumococcal Antibodies and Anti-Salmonella typhi Antibodies in a Cohort of Patients with Recurrent InfectionsGiorgia Bucciol, Heidi Schaballie, Rik Schrijvers, et al.
Clinical Genetics|June 24, 2021
Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancyChristina K Rapp, Ine Van Dijck, Lucia Laugwitz, et al.
Thorax|February 12, 2022
Acute exacerbations in children's interstitial lung diseaseElias Seidl, Nicolaus Schwerk, Julia Carlens, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2022
Severity of the S1251N allele in cystic fibrosis is affected by the presence of the F508C variant in cisSenne Cuyx, Sofia S Ramalho, Isabelle Callebaut, et al.
Pageof 12