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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 15, 1984
Hypoxanthine and xanthine concentrations determined by high performance liquid chromatography in biological fluids from patients with xanthinuria
R Boulieu, C Bory, P Baltassat, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
alpha-Aminoadipic and alpha-ketoadipic aciduria: detection of a new case by a screening program using two-dimensional thin layer chromatography of amino acids
C Vianey-Liaud, P Divry, J Cotte, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Succinyl-CoA:acetoacetate transferase deficiency. Identification of a new case; prenatal exclusion in three further pregnancies
M O Rolland, N Guffon, G Mandon, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
The inborn errors of mitochondrial fatty acid oxidation
C Vianey-Liaud, P Divry, N Gregersen, et al.
Annales De Biologie Clinique
|
January 1, 1991
[Lysine metabolism in man]
C Vianey-Liaud, P Divry, C Poinas, et al.
Annales De Biologie Clinique
|
January 1, 1977
[Hyperglycinemia without ketosis. Biochemical and enzymatic study]
N Dingeon, M O Rolland, P Divry, et al.
Presse Medicale (Paris, France : 1983)
|
January 30, 1988
[N-acetylaspartic aciduria: a new form of demyelinating encephalopathy]
C Gay, P Divry, V Macabeo, et al.
Annals of Neurology
|
January 1, 1993
3-Methylglutaconic aciduria in "optic atrophy plus"
H Costeff, O Elpeleg, N Apter, et al.
Journal De Radiologie, D'Electrologie, Et De Medecine Nucleaire
|
August 1, 1974
[Eso-gastro-duodenal radiography with moderate contrast and high voltage]
C Tavernier, P Divry, R Jauneau, et al.
Giornale Italiano Di Dermatolotia. Minerva Dermatologica
|
February 1, 1970
[Study of tumoral, cutaneous and visceral distribution of sulfur 35 in intravenous administration to patients with melanomas]
H Thiers, B Lahneche, R Verot, et al.
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of 12
Search research articles
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Showing results (21-30 of 114) with videos related to
Sort By:
Page
of 12
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 15, 1984
Hypoxanthine and xanthine concentrations determined by high performance liquid chromatography in biological fluids from patients with xanthinuria
R Boulieu, C Bory, P Baltassat, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
alpha-Aminoadipic and alpha-ketoadipic aciduria: detection of a new case by a screening program using two-dimensional thin layer chromatography of amino acids
C Vianey-Liaud, P Divry, J Cotte, et al.
Journal of Inherited Metabolic Disease
|
October 8, 1998
Succinyl-CoA:acetoacetate transferase deficiency. Identification of a new case; prenatal exclusion in three further pregnancies
M O Rolland, N Guffon, G Mandon, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
The inborn errors of mitochondrial fatty acid oxidation
C Vianey-Liaud, P Divry, N Gregersen, et al.
Annales De Biologie Clinique
|
January 1, 1991
[Lysine metabolism in man]
C Vianey-Liaud, P Divry, C Poinas, et al.
Annales De Biologie Clinique
|
January 1, 1977
[Hyperglycinemia without ketosis. Biochemical and enzymatic study]
N Dingeon, M O Rolland, P Divry, et al.
Presse Medicale (Paris, France : 1983)
|
January 30, 1988
[N-acetylaspartic aciduria: a new form of demyelinating encephalopathy]
C Gay, P Divry, V Macabeo, et al.
Annals of Neurology
|
January 1, 1993
3-Methylglutaconic aciduria in "optic atrophy plus"
H Costeff, O Elpeleg, N Apter, et al.
Journal De Radiologie, D'Electrologie, Et De Medecine Nucleaire
|
August 1, 1974
[Eso-gastro-duodenal radiography with moderate contrast and high voltage]
C Tavernier, P Divry, R Jauneau, et al.
Giornale Italiano Di Dermatolotia. Minerva Dermatologica
|
February 1, 1970
[Study of tumoral, cutaneous and visceral distribution of sulfur 35 in intravenous administration to patients with melanomas]
H Thiers, B Lahneche, R Verot, et al.
Page
of 12