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Annales De Biologie Clinique
|
January 1, 1991
[Inborn errors of lysine metabolism]
P Divry, C Vianey-Liaud, M Mathieu
Biomedical & Environmental Mass Spectrometry
|
November 1, 1987
Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year period
P Divry, C Vianey-Liaud, J Cotte
Journal of Inherited Metabolic Disease
|
January 1, 1984
Gas chromatography--mass spectrometry (GC--MS) diagnosis of two cases of medium chain acyl-CoA dehydrogenase deficiency
P Divry, C Vianey-Liaud, J Cotte
Neuropediatrics
|
May 1, 1989
Spongy degeneration of the neuraxis (Canavan-van Bogaert disease) and N-acetylaspartic aciduria
B Echenne, P Divry, C Vianey-Liaud
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.
Pathologie-Biologie
|
April 1, 1986
[Determination of serum proline iminopeptidase activity using a fluorescent substrate in patients with Paget's disease and prostatic bone metastases. Preliminary results]
M Bouvier, F Colson, J Tebib, et al.
Archives Francaises De Pediatrie
|
December 1, 1988
[Protein intolerance with lysinuria. Value of orotic aciduria in adjusting treatment with citrulline]
L de Parscau, C Vianey-Liaud, M Hermier, et al.
Journal De Genetique Humaine
|
January 1, 1988
[Genetic heterogeneity of cystinuria. Study of 12 families]
J Nissiotou, C Vianey-Liaud, B Parchoux, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 30, 1987
Hemoglobin J-Baltimore (beta 16(A13)Gly----Asp): interference with the assay of HbA1c
F Vandenesch, F Baklouti, A Francina, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Annales De Biologie Clinique
|
January 1, 1991
[Inborn errors of lysine metabolism]
P Divry, C Vianey-Liaud, M Mathieu
Biomedical & Environmental Mass Spectrometry
|
November 1, 1987
Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year period
P Divry, C Vianey-Liaud, J Cotte
Journal of Inherited Metabolic Disease
|
January 1, 1984
Gas chromatography--mass spectrometry (GC--MS) diagnosis of two cases of medium chain acyl-CoA dehydrogenase deficiency
P Divry, C Vianey-Liaud, J Cotte
Neuropediatrics
|
May 1, 1989
Spongy degeneration of the neuraxis (Canavan-van Bogaert disease) and N-acetylaspartic aciduria
B Echenne, P Divry, C Vianey-Liaud
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.
Pathologie-Biologie
|
April 1, 1986
[Determination of serum proline iminopeptidase activity using a fluorescent substrate in patients with Paget's disease and prostatic bone metastases. Preliminary results]
M Bouvier, F Colson, J Tebib, et al.
Archives Francaises De Pediatrie
|
December 1, 1988
[Protein intolerance with lysinuria. Value of orotic aciduria in adjusting treatment with citrulline]
L de Parscau, C Vianey-Liaud, M Hermier, et al.
Journal De Genetique Humaine
|
January 1, 1988
[Genetic heterogeneity of cystinuria. Study of 12 families]
J Nissiotou, C Vianey-Liaud, B Parchoux, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 30, 1987
Hemoglobin J-Baltimore (beta 16(A13)Gly----Asp): interference with the assay of HbA1c
F Vandenesch, F Baklouti, A Francina, et al.
Page
of 2