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Roderick H J Houwen

Showing results (21-30 of 100) with videos related to

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The Journal of Pediatrics|August 18, 2009
Gastric acid inhibition for fat malabsorption or gastroesophageal reflux disease in cystic fibrosis: longitudinal effect on bacterial colonization and pulmonary functionHubert P J van der Doef, Hubertus G M Arets, Steven P Froeling, et al.
World Journal of Gastroenterology|November 14, 2013
Children with celiac disease and high tTGA are genetically and phenotypically differentAmani Mubarak, Eric Spierings, Victorien M Wolters, et al.
World Journal of Gastroenterology|September 13, 2012
Tissue transglutaminase levels above 100 U/mL and celiac disease: a prospective studyAmani Mubarak, Victorien M Wolters, Frits H J Gmelig-Meyling, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 3, 2016
Ursodeoxycholic acid treatment is associated with improvement of liver stiffness in cystic fibrosis patientsCathelijne van der Feen, Hubert P J van der Doef, Cornelis K van der Ent, et al.
Current Gastroenterology Reports|March 9, 2011
Intestinal obstruction syndromes in cystic fibrosis: meconium ileus, distal intestinal obstruction syndrome, and constipationHubert P J van der Doef, Freddy T M Kokke, Cornelis K van der Ent, et al.
Hepatology (Baltimore, Md.)|September 5, 2009
Long-term exclusive zinc monotherapy in symptomatic Wilson disease: experience in 17 patientsFrancisca H H Linn, Roderick H J Houwen, Jan van Hattum, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 15, 2013
The relationship between body growth and pulmonary function in children with cystic fibrosisJanna W Woestenenk, Rebecca K Stellato, Suzanne W Terheggen-Lagro, et al.
The British Journal of Nutrition|November 17, 2018
Vitamin D intake, serum 25-hydroxy vitamin D and pulmonary function in paediatric patients with cystic fibrosis: a longitudinal approachNyanza K L M Timmers, Rebecca K Stellato, Cornelis K van der Ent, et al.
Journal of Inherited Metabolic Disease|October 12, 2019
Inborn errors of enzymes in glutamate metabolismLynne Rumping, Esmee Vringer, Roderick H J Houwen, et al.
Clinical Nutrition (Edinburgh, Scotland)|May 16, 2015
Vitamin A intake and serum retinol levels in children and adolescents with cystic fibrosisJanna W Woestenenk, Nancy Broos, Rebecca K Stellato, et al.
Pageof 10

Showing results (21-30 of 100) with videos related to

Sort By:
Pageof 10
The Journal of Pediatrics|August 18, 2009
Gastric acid inhibition for fat malabsorption or gastroesophageal reflux disease in cystic fibrosis: longitudinal effect on bacterial colonization and pulmonary functionHubert P J van der Doef, Hubertus G M Arets, Steven P Froeling, et al.
World Journal of Gastroenterology|November 14, 2013
Children with celiac disease and high tTGA are genetically and phenotypically differentAmani Mubarak, Eric Spierings, Victorien M Wolters, et al.
World Journal of Gastroenterology|September 13, 2012
Tissue transglutaminase levels above 100 U/mL and celiac disease: a prospective studyAmani Mubarak, Victorien M Wolters, Frits H J Gmelig-Meyling, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 3, 2016
Ursodeoxycholic acid treatment is associated with improvement of liver stiffness in cystic fibrosis patientsCathelijne van der Feen, Hubert P J van der Doef, Cornelis K van der Ent, et al.
Current Gastroenterology Reports|March 9, 2011
Intestinal obstruction syndromes in cystic fibrosis: meconium ileus, distal intestinal obstruction syndrome, and constipationHubert P J van der Doef, Freddy T M Kokke, Cornelis K van der Ent, et al.
Hepatology (Baltimore, Md.)|September 5, 2009
Long-term exclusive zinc monotherapy in symptomatic Wilson disease: experience in 17 patientsFrancisca H H Linn, Roderick H J Houwen, Jan van Hattum, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 15, 2013
The relationship between body growth and pulmonary function in children with cystic fibrosisJanna W Woestenenk, Rebecca K Stellato, Suzanne W Terheggen-Lagro, et al.
The British Journal of Nutrition|November 17, 2018
Vitamin D intake, serum 25-hydroxy vitamin D and pulmonary function in paediatric patients with cystic fibrosis: a longitudinal approachNyanza K L M Timmers, Rebecca K Stellato, Cornelis K van der Ent, et al.
Journal of Inherited Metabolic Disease|October 12, 2019
Inborn errors of enzymes in glutamate metabolismLynne Rumping, Esmee Vringer, Roderick H J Houwen, et al.
Clinical Nutrition (Edinburgh, Scotland)|May 16, 2015
Vitamin A intake and serum retinol levels in children and adolescents with cystic fibrosisJanna W Woestenenk, Nancy Broos, Rebecca K Stellato, et al.
Pageof 10