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Journal of Neurochemistry
|
September 1, 1995
Excess extracellular and low intracellular glutamate in poorly differentiating wobbler astrocytes and astrocyte recovery in glutamine-depleted culture medium
D Hantaz-Ambroise, D Cambier, A Aït-Ikhlef, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Attempt at therapy in sulphite oxidase deficiency
P 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 complementation
F 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 hyperammonemia
F 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 male
L 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 aciduria
P 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 II
L Vilarinho, R Araujo, A Vilarinho, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Dicarboxylic aminoaciduria
P Kamoun, P Parvy, D Rabier, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 64) with videos related to
Sort By:
Page
of 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 medium
D Hantaz-Ambroise, D Cambier, A Aït-Ikhlef, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Attempt at therapy in sulphite oxidase deficiency
P 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 complementation
F 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 hyperammonemia
F 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 male
L 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 aciduria
P 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 II
L Vilarinho, R Araujo, A Vilarinho, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Dicarboxylic aminoaciduria
P Kamoun, P Parvy, D Rabier, et al.
Page
of 7