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H J Veeze

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The Journal of Clinical Investigation|February 1, 1994
Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotypeH J Veeze, D J Halley, J Bijman, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1997
Clinical use of acid steatocritA Van den Neucker, N Pestel, T M Tran, et al.
Clinical Endocrinology|September 12, 2009
Revisiting infant growth prior to childhood onset type 1 diabetesA V Kharagjitsingh, M A J de Ridder, B O Roep, et al.
Human Reproduction (Oxford, England)|April 1, 1999
The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic dataG R Dohle, H J Veeze, S E Overbeek, et al.
Transplantation Proceedings|December 1, 1990
In vivo electrophysiologic evaluation of intestinal grafts in dogsM A Meijssen, E Heineman, K Fischer, et al.
Human Genetics|September 1, 1990
The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosisD J Halley, H J Veeze, L A Sandkuyl, et al.
Gastroenterology|July 13, 2000
Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study ConsortiumI Bronsveld, F Mekus, J Bijman, et al.
The Journal of Clinical Investigation|December 26, 2001
Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblingsI Bronsveld, F Mekus, J Bijman, et al.
Gut|November 1, 1991
Value of in vivo electrophysiological measurements to evaluate canine small bowel autotransplantsM A Meijssen, E Heineman, R W de Bruin, et al.
Pediatric Diabetes|March 24, 2017
Seasonality at the clinical onset of type 1 diabetes-Lessons from the SWEET databaseA Gerasimidi Vazeou, O Kordonouri, M Witsch, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The Journal of Clinical Investigation|February 1, 1994
Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotypeH J Veeze, D J Halley, J Bijman, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1997
Clinical use of acid steatocritA Van den Neucker, N Pestel, T M Tran, et al.
Clinical Endocrinology|September 12, 2009
Revisiting infant growth prior to childhood onset type 1 diabetesA V Kharagjitsingh, M A J de Ridder, B O Roep, et al.
Human Reproduction (Oxford, England)|April 1, 1999
The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic dataG R Dohle, H J Veeze, S E Overbeek, et al.
Transplantation Proceedings|December 1, 1990
In vivo electrophysiologic evaluation of intestinal grafts in dogsM A Meijssen, E Heineman, K Fischer, et al.
Human Genetics|September 1, 1990
The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosisD J Halley, H J Veeze, L A Sandkuyl, et al.
Gastroenterology|July 13, 2000
Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study ConsortiumI Bronsveld, F Mekus, J Bijman, et al.
The Journal of Clinical Investigation|December 26, 2001
Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblingsI Bronsveld, F Mekus, J Bijman, et al.
Gut|November 1, 1991
Value of in vivo electrophysiological measurements to evaluate canine small bowel autotransplantsM A Meijssen, E Heineman, R W de Bruin, et al.
Pediatric Diabetes|March 24, 2017
Seasonality at the clinical onset of type 1 diabetes-Lessons from the SWEET databaseA Gerasimidi Vazeou, O Kordonouri, M Witsch, et al.
Pageof 3