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Peter Witters

Showing results (1-10 of 73) with videos related to

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Metabolites|May 28, 2022
Understanding Inborn Errors of Metabolism through MetabolomicsKaren Driesen, Peter Witters
Molecular Genetics and Metabolism|September 29, 2018
Central nervous involvement is common in PGM1-CDGSilvia Radenkovic, Peter Witters, Eva Morava
Nutrients|November 8, 2017
Nutritional Therapies in Congenital Disorders of Glycosylation (CDG)Peter Witters, David Cassiman, Eva Morava
Cardiology in the Young|September 21, 2016
A rare cause of persisting anaemia in a patient with a failing Fontan circulationLoes Lambrecht, Bjorn Cools, Peter Witters
Molecular Genetics and Metabolism|March 15, 2024
Glycosphingolipids in congenital disorders of glycosylation (CDG)Andrea Jáñez Pedrayes, Daisy Rymen, Bart Ghesquière, et al.
European Journal of Pediatrics|April 9, 2016
Beyond pancreatic insufficiency and liver disease in cystic fibrosisStephanie Demeyer, Kris De Boeck, Peter Witters, et al.
Molecular Genetics and Metabolism Reports|June 12, 2025
Adrenal insufficiency in inborn errors of metabolism and vice versa: Case reports and review of the literatureAriane De Preter, Anne Rochtus, Peter Witters, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|April 7, 2018
Long-term outcome of transjugular intrahepatic portosystemic shunt for portal hypertension in autosomal recessive polycystic kidney diseaseSarah Verbeeck, Djalila Mekhali, David Cassiman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2019
Therapeutic approaches in Congenital Disorders of Glycosylation (CDG) involving N-linked glycosylation: an updateJan Verheijen, Shawn Tahata, Tamas Kozicz, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 16, 2021
Comparative meta-analysis of cystic fibrosis cell models suggests partial endothelial-to-mesenchymal transitionLucas Treps, Mathias Declercq, Siham Bousfia, et al.
Pageof 8

Showing results (1-10 of 73) with videos related to

Sort By:
Pageof 8
Metabolites|May 28, 2022
Understanding Inborn Errors of Metabolism through MetabolomicsKaren Driesen, Peter Witters
Molecular Genetics and Metabolism|September 29, 2018
Central nervous involvement is common in PGM1-CDGSilvia Radenkovic, Peter Witters, Eva Morava
Nutrients|November 8, 2017
Nutritional Therapies in Congenital Disorders of Glycosylation (CDG)Peter Witters, David Cassiman, Eva Morava
Cardiology in the Young|September 21, 2016
A rare cause of persisting anaemia in a patient with a failing Fontan circulationLoes Lambrecht, Bjorn Cools, Peter Witters
Molecular Genetics and Metabolism|March 15, 2024
Glycosphingolipids in congenital disorders of glycosylation (CDG)Andrea Jáñez Pedrayes, Daisy Rymen, Bart Ghesquière, et al.
European Journal of Pediatrics|April 9, 2016
Beyond pancreatic insufficiency and liver disease in cystic fibrosisStephanie Demeyer, Kris De Boeck, Peter Witters, et al.
Molecular Genetics and Metabolism Reports|June 12, 2025
Adrenal insufficiency in inborn errors of metabolism and vice versa: Case reports and review of the literatureAriane De Preter, Anne Rochtus, Peter Witters, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|April 7, 2018
Long-term outcome of transjugular intrahepatic portosystemic shunt for portal hypertension in autosomal recessive polycystic kidney diseaseSarah Verbeeck, Djalila Mekhali, David Cassiman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2019
Therapeutic approaches in Congenital Disorders of Glycosylation (CDG) involving N-linked glycosylation: an updateJan Verheijen, Shawn Tahata, Tamas Kozicz, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 16, 2021
Comparative meta-analysis of cystic fibrosis cell models suggests partial endothelial-to-mesenchymal transitionLucas Treps, Mathias Declercq, Siham Bousfia, et al.
Pageof 8