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Archives Francaises De Pediatrie
|
July 1, 1979
[Hyperammonemia in pediatric diseases]
L Cathelineau
Advances in Experimental Medicine and Biology
|
January 1, 1982
Sparse-fur mutation: a model for some human ornithine transcarbamylase deficiencies
P Briand, L Cathelineau
Soins; La Revue De Reference Infirmiere
|
November 1, 1989
[Artificial ventilation in severe bronchodysplasia after resuscitation. Admission in a medium-term pediatric service]
L Cathelineau, C Hermabessière
Medecine & Chirurgie Digestives
|
January 1, 1972
[Hyperammoniemia caused by genotypic enzymopathies]
L Cathelineau, C Polonovski
Biologie Et Gastro-Enterologie
|
January 1, 1972
[Qualitative study by electrophoresis and chromatography of pepsins in the gastric juice of infants and children]
L Cathelineau, N Desquilbet, C Polonovski
Advances in Experimental Medicine and Biology
|
January 1, 1982
Immunochemical assay in 16 boys with ornithine transcarbamylase deficiency
B Francois, P Briand, L Cathelineau
Pediatric Research
|
March 1, 1979
Lack of mitochondrial enzymes of the urea cycle in human white blood cells
D Rabier, L Cathelineau, P Kamoun
Annales De Biologie Clinique
|
January 1, 1978
[Rapid preparation of ornithine carbamyl transferase without carbamyl phosphate synthetase activity (author's transl)]
D Rabier, L Cathelineau, P Kamoun
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 1, 1972
Ornithine carbamyl transferase: the effects of pH on the kinetics of a mutant human enzyme
L Cathelineau, J M Saudubray, C Polonovski
Enzyme
|
January 1, 1974
Heterogenous mutations of the structural gene of human ornithine carbamyltransferase as observed in five personal cases
L Cathelineau, J M Saudubray, C Polonovski
Page
of 7
Search research articles
Search
Showing results (1-10 of 65) with videos related to
Sort By:
Page
of 7
Archives Francaises De Pediatrie
|
July 1, 1979
[Hyperammonemia in pediatric diseases]
L Cathelineau
Advances in Experimental Medicine and Biology
|
January 1, 1982
Sparse-fur mutation: a model for some human ornithine transcarbamylase deficiencies
P Briand, L Cathelineau
Soins; La Revue De Reference Infirmiere
|
November 1, 1989
[Artificial ventilation in severe bronchodysplasia after resuscitation. Admission in a medium-term pediatric service]
L Cathelineau, C Hermabessière
Medecine & Chirurgie Digestives
|
January 1, 1972
[Hyperammoniemia caused by genotypic enzymopathies]
L Cathelineau, C Polonovski
Biologie Et Gastro-Enterologie
|
January 1, 1972
[Qualitative study by electrophoresis and chromatography of pepsins in the gastric juice of infants and children]
L Cathelineau, N Desquilbet, C Polonovski
Advances in Experimental Medicine and Biology
|
January 1, 1982
Immunochemical assay in 16 boys with ornithine transcarbamylase deficiency
B Francois, P Briand, L Cathelineau
Pediatric Research
|
March 1, 1979
Lack of mitochondrial enzymes of the urea cycle in human white blood cells
D Rabier, L Cathelineau, P Kamoun
Annales De Biologie Clinique
|
January 1, 1978
[Rapid preparation of ornithine carbamyl transferase without carbamyl phosphate synthetase activity (author's transl)]
D Rabier, L Cathelineau, P Kamoun
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 1, 1972
Ornithine carbamyl transferase: the effects of pH on the kinetics of a mutant human enzyme
L Cathelineau, J M Saudubray, C Polonovski
Enzyme
|
January 1, 1974
Heterogenous mutations of the structural gene of human ornithine carbamyltransferase as observed in five personal cases
L Cathelineau, J M Saudubray, C Polonovski
Page
of 7