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

P Parvy

Showing results (41-50 of 64) with videos related to

Pageof 7
Sort By:
Journal of Neurochemistry|September 1, 1995
Excess extracellular and low intracellular glutamate in poorly differentiating wobbler astrocytes and astrocyte recovery in glutamine-depleted culture mediumD Hantaz-Ambroise, D Cambier, A Aït-Ikhlef, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Attempt at therapy in sulphite oxidase deficiencyP Tardy, P Parvy, C Charpentier, et al.
Biochemical and Biophysical Research Communications|July 18, 1983
Characterization of enzymatic deficiencies of branched chain amino-acid catabolism in human fibroblasts by genetic complementationF X Coudé, G Grimber, P Parvy, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 7, 1998
[Variation of amino acids in relation to age in Down syndrome subjects]C Mircher, A Salabelle, M A Peeters, et al.
Pediatric Research|June 1, 1981
A mechanism for valproate-induced hyperammonemiaF X Coude, D Rabier, L Cathelineau, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A new case of argininaemia without spastic diplegia in a Portuguese maleL Vilarinho, V Senra, A Vilarinho, et al.
Clinical Chemistry|November 1, 1995
Free amino acids in amniotic fluid and the prenatal diagnosis of homocystinuria with methylmalonic aciduriaP Parvy, J Bardet, B Chadefaux-Vekemans, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Do criteria exist from urinary organic acids to distinguish beta-oxidation defects?D Rabier, J Bardet, P Parvy, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
A new case of hyperoxaluria type IIL Vilarinho, R Araujo, A Vilarinho, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Dicarboxylic aminoaciduriaP Kamoun, P Parvy, D Rabier, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
Journal of Neurochemistry|September 1, 1995
Excess extracellular and low intracellular glutamate in poorly differentiating wobbler astrocytes and astrocyte recovery in glutamine-depleted culture mediumD Hantaz-Ambroise, D Cambier, A Aït-Ikhlef, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Attempt at therapy in sulphite oxidase deficiencyP Tardy, P Parvy, C Charpentier, et al.
Biochemical and Biophysical Research Communications|July 18, 1983
Characterization of enzymatic deficiencies of branched chain amino-acid catabolism in human fibroblasts by genetic complementationF X Coudé, G Grimber, P Parvy, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 7, 1998
[Variation of amino acids in relation to age in Down syndrome subjects]C Mircher, A Salabelle, M A Peeters, et al.
Pediatric Research|June 1, 1981
A mechanism for valproate-induced hyperammonemiaF X Coude, D Rabier, L Cathelineau, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
A new case of argininaemia without spastic diplegia in a Portuguese maleL Vilarinho, V Senra, A Vilarinho, et al.
Clinical Chemistry|November 1, 1995
Free amino acids in amniotic fluid and the prenatal diagnosis of homocystinuria with methylmalonic aciduriaP Parvy, J Bardet, B Chadefaux-Vekemans, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Do criteria exist from urinary organic acids to distinguish beta-oxidation defects?D Rabier, J Bardet, P Parvy, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
A new case of hyperoxaluria type IIL Vilarinho, R Araujo, A Vilarinho, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Dicarboxylic aminoaciduriaP Kamoun, P Parvy, D Rabier, et al.
Pageof 7