Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Hendrickx

Showing results (71-80 of 91) with videos related to

Pageof 10
Sort By:
Anesthesiology|October 1, 1988
Alfentanil pharmacokinetics and metabolism in humansW Meuldermans, A Van Peer, J Hendrickx, et al.
Genomics|June 1, 1994
Localization of a new type of X-linked liver glycogenosis to the chromosomal region Xp22 containing the liver alpha-subunit of phosphorylase kinase (PHKA2)J Hendrickx, P Coucke, M C Hors-Cayla, et al.
Chemioterapia : International Journal of the Mediterranean Society of Chemotherapy|August 1, 1988
Single-dose prophylaxis with cefotetan in elective abdominal surgery. A controlled trialJ A Gruwez, J Lerut, M R Christiaens, et al.
Anesthesiology|October 1, 1988
Is the metabolism of alfentanil subject to debrisoquine polymorphism? A study using human liver microsomesK L Lavrijsen, J M Van Houdt, D M Van Dyck, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2W Wuyts, W Van Hul, J Hendrickx, et al.
B-ENT|January 30, 2008
Prevalence of tinnitus and audiometric shapeK Demeester, A van Wieringen, J J Hendrickx, et al.
Journal of Chemotherapy (Florence, Italy)|July 1, 1989
Single-dose prophylaxis with cefotetan in elective abdominal surgery. A controlled trialJ A Gruwez, J Lerut, M R Christiaens, et al.
Clinical Genetics|February 1, 1991
Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patientsJ G Wauters, J Hendrickx, P Coucke, et al.
Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.
Genomics|April 1, 1991
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22P J Willems, J Hendrickx, B J Van der Auwera, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
Anesthesiology|October 1, 1988
Alfentanil pharmacokinetics and metabolism in humansW Meuldermans, A Van Peer, J Hendrickx, et al.
Genomics|June 1, 1994
Localization of a new type of X-linked liver glycogenosis to the chromosomal region Xp22 containing the liver alpha-subunit of phosphorylase kinase (PHKA2)J Hendrickx, P Coucke, M C Hors-Cayla, et al.
Chemioterapia : International Journal of the Mediterranean Society of Chemotherapy|August 1, 1988
Single-dose prophylaxis with cefotetan in elective abdominal surgery. A controlled trialJ A Gruwez, J Lerut, M R Christiaens, et al.
Anesthesiology|October 1, 1988
Is the metabolism of alfentanil subject to debrisoquine polymorphism? A study using human liver microsomesK L Lavrijsen, J M Van Houdt, D M Van Dyck, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Identification and characterization of a novel member of the EXT gene family, EXTL2W Wuyts, W Van Hul, J Hendrickx, et al.
B-ENT|January 30, 2008
Prevalence of tinnitus and audiometric shapeK Demeester, A van Wieringen, J J Hendrickx, et al.
Journal of Chemotherapy (Florence, Italy)|July 1, 1989
Single-dose prophylaxis with cefotetan in elective abdominal surgery. A controlled trialJ A Gruwez, J Lerut, M R Christiaens, et al.
Clinical Genetics|February 1, 1991
Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patientsJ G Wauters, J Hendrickx, P Coucke, et al.
Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.
Genomics|April 1, 1991
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22P J Willems, J Hendrickx, B J Van der Auwera, et al.
Pageof 10