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

C Dorche

Showing results (1-10 of 48) with videos related to

Pageof 5
Sort By:
Prenatal Diagnosis|May 18, 1999
Molybdenum cofactor deficiency: first prenatal genetic analysisJ Reiss, E Christensen, C Dorche
Archives of Biochemistry and Biophysics|November 1, 1990
Studies on the interaction of a thiol-dependent hydrogen peroxide scavenging enzyme and phenylalanine hydroxylaseS Milstien, C Dorche, S Kaufman
Bulletin De La Societe De Chimie Biologique|January 1, 1970
[Glucose-6-phosphate dehydrogenase Debrousse type: problem of enzymatic type specific to Algerians of the Arabic race]C Kissin, C Dorche, J Cotte
Pathologie-Biologie|January 1, 1970
[Fluorescimetric determination of blood tyrosine]C Collombel, C Dorche, P Baltassat
Pediatric Research|July 1, 1974
Futher studies on the nature of phenylalanine hydroxylation in brainJ P Abita, C Dorche, S Kaufman
Archives Francaises De Pediatrie|June 1, 1993
[Cystic fibrosis: what is the incidence?]J P Farriaux, C Dorche, G Travert
European Journal of Pediatrics|August 1, 1993
Molybdenum cofactor deficiency in two siblings: diagnostic difficultiesL K Hansen, K Wulff, C Dorche, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|July 1, 1979
[Neonatal screening for congenital hypothyroidism by measuring TSH in dried blood samples. Two years experience in the method (author's transl)]M David, C Dorche, G Teyssier, et al.
European Journal of Toxicology|January 1, 1970
[Systematic detection at birth of drug-induced hemolytic anemia caused by a toxic mechanism linked to an erythrocyte deficiency of glucose-6-phosphate dehydrogenase]C Collombel, C Kissen, C Dorche, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Neonatal screening for congenital adrenal hyperplasia: a pilot study in FranceJ L Dhondt, C Dorche, J P Farriaux, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Prenatal Diagnosis|May 18, 1999
Molybdenum cofactor deficiency: first prenatal genetic analysisJ Reiss, E Christensen, C Dorche
Archives of Biochemistry and Biophysics|November 1, 1990
Studies on the interaction of a thiol-dependent hydrogen peroxide scavenging enzyme and phenylalanine hydroxylaseS Milstien, C Dorche, S Kaufman
Bulletin De La Societe De Chimie Biologique|January 1, 1970
[Glucose-6-phosphate dehydrogenase Debrousse type: problem of enzymatic type specific to Algerians of the Arabic race]C Kissin, C Dorche, J Cotte
Pathologie-Biologie|January 1, 1970
[Fluorescimetric determination of blood tyrosine]C Collombel, C Dorche, P Baltassat
Pediatric Research|July 1, 1974
Futher studies on the nature of phenylalanine hydroxylation in brainJ P Abita, C Dorche, S Kaufman
Archives Francaises De Pediatrie|June 1, 1993
[Cystic fibrosis: what is the incidence?]J P Farriaux, C Dorche, G Travert
European Journal of Pediatrics|August 1, 1993
Molybdenum cofactor deficiency in two siblings: diagnostic difficultiesL K Hansen, K Wulff, C Dorche, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|July 1, 1979
[Neonatal screening for congenital hypothyroidism by measuring TSH in dried blood samples. Two years experience in the method (author's transl)]M David, C Dorche, G Teyssier, et al.
European Journal of Toxicology|January 1, 1970
[Systematic detection at birth of drug-induced hemolytic anemia caused by a toxic mechanism linked to an erythrocyte deficiency of glucose-6-phosphate dehydrogenase]C Collombel, C Kissen, C Dorche, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Neonatal screening for congenital adrenal hyperplasia: a pilot study in FranceJ L Dhondt, C Dorche, J P Farriaux, et al.
Pageof 5