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F W de Rooij

Showing results (11-20 of 23) with videos related to

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Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 1, 1991
The selenium-75-homocholic acid taurine test reevaluated: combined measurement of fecal selenium-75 activity and 3 alpha-hydroxy bile acids in 211 patientsA J van Tilburg, F W de Rooij, J W van den Berg, et al.
Acta Paediatrica Scandinavica. Supplement|January 1, 1985
Bile acid malabsorption in cystic fibrosis; membrane vesicles, a tool for revealing the role of the ileal brush border membraneF W de Rooij, J W van den Berg, M Sinaasappel, et al.
Gastroenterology|January 1, 1990
Na+-dependent bile acid transport in the ileum: the balance between diarrhea and constipationA J van Tilburg, F W de Rooij, M van Blankenstein, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 29, 1998
[Endoscopic treatment of Barrett esophagus]P Hinnen, J Dees, F W De Rooij, et al.
Lasers in Surgery and Medicine|February 26, 1999
Kinetics, localization, and mechanism of 5-aminolevulinic acid-induced porphyrin accumulation in normal and Barrett's-like rat esophagusJ van den Boogert, A B Houtsmuller, F W de Rooij, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyriaC Picat, M H Delfau, F W de Rooij, et al.
The Journal of Clinical Investigation|November 1, 1990
Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyriaM H Delfau, C Picat, F W de Rooij, et al.
British Journal of Cancer|September 23, 1998
Biochemical basis of 5-aminolaevulinic acid-induced protoporphyrin IX accumulation: a study in patients with (pre)malignant lesions of the oesophagusP Hinnen, F W de Rooij, M L van Velthuysen, et al.
Human Mutation|January 15, 1999
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation updateR Rosipal, J Lamoril, H Puy, et al.
British Journal of Cancer|August 17, 2000
Porphyrin biosynthesis in human Barrett's oesophagus and adenocarcinoma after ingestion of 5-aminolaevulinic acidP Hinnen, F W de Rooij, E M Terlouw, et al.
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Showing results (11-20 of 23) with videos related to

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Pageof 3
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|June 1, 1991
The selenium-75-homocholic acid taurine test reevaluated: combined measurement of fecal selenium-75 activity and 3 alpha-hydroxy bile acids in 211 patientsA J van Tilburg, F W de Rooij, J W van den Berg, et al.
Acta Paediatrica Scandinavica. Supplement|January 1, 1985
Bile acid malabsorption in cystic fibrosis; membrane vesicles, a tool for revealing the role of the ileal brush border membraneF W de Rooij, J W van den Berg, M Sinaasappel, et al.
Gastroenterology|January 1, 1990
Na+-dependent bile acid transport in the ileum: the balance between diarrhea and constipationA J van Tilburg, F W de Rooij, M van Blankenstein, et al.
Nederlands Tijdschrift Voor Geneeskunde|December 29, 1998
[Endoscopic treatment of Barrett esophagus]P Hinnen, J Dees, F W De Rooij, et al.
Lasers in Surgery and Medicine|February 26, 1999
Kinetics, localization, and mechanism of 5-aminolevulinic acid-induced porphyrin accumulation in normal and Barrett's-like rat esophagusJ van den Boogert, A B Houtsmuller, F W de Rooij, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Identification of the mutations in the parents of a patient with a putative compound heterozygosity for acute intermittent porphyriaC Picat, M H Delfau, F W de Rooij, et al.
The Journal of Clinical Investigation|November 1, 1990
Two different point G to A mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyriaM H Delfau, C Picat, F W de Rooij, et al.
British Journal of Cancer|September 23, 1998
Biochemical basis of 5-aminolaevulinic acid-induced protoporphyrin IX accumulation: a study in patients with (pre)malignant lesions of the oesophagusP Hinnen, F W de Rooij, M L van Velthuysen, et al.
Human Mutation|January 15, 1999
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation updateR Rosipal, J Lamoril, H Puy, et al.
British Journal of Cancer|August 17, 2000
Porphyrin biosynthesis in human Barrett's oesophagus and adenocarcinoma after ingestion of 5-aminolaevulinic acidP Hinnen, F W de Rooij, E M Terlouw, et al.
Pageof 3