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Journal of Inherited Metabolic Disease
|
June 29, 1999
Determination of total fatty acids in plasma: cis-5-tetradecenoic acid (C14:1 omega-9) in the diagnosis of long-chain fatty acid oxidation defects
P Divry, C Vianey-Saban, M Mathieu
Journal of Inherited Metabolic Disease
|
November 20, 2008
Quality of analytical performance in inherited metabolic disorders: the role of ERNDIM
B Fowler, A Burlina, V Kozich, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Stable-isotope selected-ion monitoring quantification of methylmalonic acid in dried filter-paper urine samples
J M Parnet, P Divry, C Vianey-Saban, et al.
Journal of Clinical Forensic Medicine
|
October 24, 2006
Homicide followed by freezing and burning: usefulness of measuring SCHAD (short-chain 3-hydroxyacyl-CoA dehydrogenase) activity
L Fanton, H Yappo-Ette, C Vianey-Saban, et al.
Annales De Biologie Clinique
|
June 26, 2004
[Application of tandem mass spectrometry to neonatal screening of inherited metabolic diseases: focus on present developments]
D Cheillan, S Cognat, C Vianey-Saban, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 15, 1992
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts
C Bertrand, R Dumoulin, P Divry, et al.
Forensic Science International
|
December 14, 2001
Method for determining if a corpse has been frozen: measuring the activity of short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD)
A Miras, H Yapo-Ette, C Vianey-Saban, et al.
Revue Neurologique
|
April 1, 2005
[Creatine deficiency syndromes]
D Cheillan, S Cognat, N Vandenberghe, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 11, 2013
[L-2-hydroxyglutaric aciduria: report on two cases]
S Wagner, C Vianey-Saban, G-S Salomons, et al.
Biochimica Et Biophysica Acta
|
January 22, 1993
Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts
C Bertrand, C Largillière, M T Zabot, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 68) with videos related to
Sort By:
Page
of 7
Journal of Inherited Metabolic Disease
|
June 29, 1999
Determination of total fatty acids in plasma: cis-5-tetradecenoic acid (C14:1 omega-9) in the diagnosis of long-chain fatty acid oxidation defects
P Divry, C Vianey-Saban, M Mathieu
Journal of Inherited Metabolic Disease
|
November 20, 2008
Quality of analytical performance in inherited metabolic disorders: the role of ERNDIM
B Fowler, A Burlina, V Kozich, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Stable-isotope selected-ion monitoring quantification of methylmalonic acid in dried filter-paper urine samples
J M Parnet, P Divry, C Vianey-Saban, et al.
Journal of Clinical Forensic Medicine
|
October 24, 2006
Homicide followed by freezing and burning: usefulness of measuring SCHAD (short-chain 3-hydroxyacyl-CoA dehydrogenase) activity
L Fanton, H Yappo-Ette, C Vianey-Saban, et al.
Annales De Biologie Clinique
|
June 26, 2004
[Application of tandem mass spectrometry to neonatal screening of inherited metabolic diseases: focus on present developments]
D Cheillan, S Cognat, C Vianey-Saban, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 15, 1992
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts
C Bertrand, R Dumoulin, P Divry, et al.
Forensic Science International
|
December 14, 2001
Method for determining if a corpse has been frozen: measuring the activity of short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD)
A Miras, H Yapo-Ette, C Vianey-Saban, et al.
Revue Neurologique
|
April 1, 2005
[Creatine deficiency syndromes]
D Cheillan, S Cognat, N Vandenberghe, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 11, 2013
[L-2-hydroxyglutaric aciduria: report on two cases]
S Wagner, C Vianey-Saban, G-S Salomons, et al.
Biochimica Et Biophysica Acta
|
January 22, 1993
Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts
C Bertrand, C Largillière, M T Zabot, et al.
Page
of 7