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

L Dhondt

Showing results (31-40 of 182) with videos related to

Pageof 19
Sort By:
Lille Medical : Journal De La Faculte De Medecine Et De Pharmacie De L'Universite De Lille|October 1, 1975
[Detection of female carriers of ornithine-carbamyl-transferase deficiency by measurement of orotic acid in the urine]J L Dhondt, J P Farriaux
Annales De Pediatrie|December 2, 1972
[Amino acids in the intestinal fluid in a subject with high blood phenylalanine. Comparative study with a control group]J P Farriaux, J L Dhondt
Pediatric Research|May 1, 1976
Type I hyperprolinemia: a study of the intestinal absorption of proline, hydroxyproline, and glycineJ P Farriaux, J L Dhondt
Archives Francaises De Pediatrie|October 1, 1981
[Hyperphenylalaninemia in 1981. A diagnostic approach (author's transl)]J L Dhondt, J P Farriaux
Pathologie-Biologie|June 1, 1980
[Tetrahydroblopterin. Metabolism and metabolic role of unconjugated pteridines (author's transl)]J L Dhondt, J P Farriaux
Journal of Inherited Metabolic Disease|January 1, 1981
Hepatic phenylalanine hydroxylase activity in hyperphenylalaninaemiaJ L Dhondt, J P Farriaux
Revue Medicale De Liege|May 15, 1984
[Neonatal screening of congenital hyperplasia of the adrenal glands (21-hydroxylase deficiency)]J P Farriaux, J L Dhondt
Annales De Biologie Clinique|June 10, 2000
[The wonderful history of neonatal screening]J L Dhondt, J P Farriaux
Annales De Biologie Clinique|April 9, 2002
[Screening of tetrahydrobiopterin deficiency among hyperphenylalaninemic patients]J L Dhondt, J M Hayte
Journal De Genetique Humaine|June 1, 1979
[Heterozygote detection in phenylketonuria by means of an oral load of phenylalanine]J L Dhondt, J P Farriaux
Pageof 19

Showing results (31-40 of 182) with videos related to

Sort By:
Pageof 19
Lille Medical : Journal De La Faculte De Medecine Et De Pharmacie De L'Universite De Lille|October 1, 1975
[Detection of female carriers of ornithine-carbamyl-transferase deficiency by measurement of orotic acid in the urine]J L Dhondt, J P Farriaux
Annales De Pediatrie|December 2, 1972
[Amino acids in the intestinal fluid in a subject with high blood phenylalanine. Comparative study with a control group]J P Farriaux, J L Dhondt
Pediatric Research|May 1, 1976
Type I hyperprolinemia: a study of the intestinal absorption of proline, hydroxyproline, and glycineJ P Farriaux, J L Dhondt
Archives Francaises De Pediatrie|October 1, 1981
[Hyperphenylalaninemia in 1981. A diagnostic approach (author's transl)]J L Dhondt, J P Farriaux
Pathologie-Biologie|June 1, 1980
[Tetrahydroblopterin. Metabolism and metabolic role of unconjugated pteridines (author's transl)]J L Dhondt, J P Farriaux
Journal of Inherited Metabolic Disease|January 1, 1981
Hepatic phenylalanine hydroxylase activity in hyperphenylalaninaemiaJ L Dhondt, J P Farriaux
Revue Medicale De Liege|May 15, 1984
[Neonatal screening of congenital hyperplasia of the adrenal glands (21-hydroxylase deficiency)]J P Farriaux, J L Dhondt
Annales De Biologie Clinique|June 10, 2000
[The wonderful history of neonatal screening]J L Dhondt, J P Farriaux
Annales De Biologie Clinique|April 9, 2002
[Screening of tetrahydrobiopterin deficiency among hyperphenylalaninemic patients]J L Dhondt, J M Hayte
Journal De Genetique Humaine|June 1, 1979
[Heterozygote detection in phenylketonuria by means of an oral load of phenylalanine]J L Dhondt, J P Farriaux
Pageof 19