Search research articles
Contact Us
Filters
Showing results (31-40 of 55) with videos related to
Page
of 6
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 12, 1973
Propionic acid, an artefact which can leave methylmalonic acidemia undiscovered
M Duran, D Ketting, S K Wadman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 16, 1976
Glutaric aciduria type II: report on a previously undescribed metabolic disorder
H Przyrembel, U Wendel, K Becker, et al.
Journal of Chromatography
|
August 21, 1979
Urinary excretion of methylated purines in man and in the rat after the administration of theophylline
A H van Gennip, J Grift, E J van Bree-Blom, et al.
European Journal of Pediatrics
|
June 28, 1979
Two sisters with isovaleric acidaemia, multiple attacks of ketoacidosis and normal development
M Duran, F J van Sprang, J G Drewes, et al.
European Journal of Pediatrics
|
July 1, 1982
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs
F A Beemer, K Bartlett, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 18, 1981
Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia
R Berger, G P Smit, S A Stoker-de Vries, et al.
The Journal of Pediatrics
|
January 1, 1979
Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase
R B Schutgens, H Heymans, A Ketel, et al.
The Journal of Pediatrics
|
December 1, 1979
3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency: postnatal management following prenatal diagnosis by analysis of maternal urine
M Duran, R B Schutgens, A Ketel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 15, 1985
Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids
M Duran, D Ketting, R van Vossen, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1982
Isovaleric acidaemia presenting with dwarfism, cataract and congenital abnormalities
M Duran, L Bruinvis, D Ketting, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 55) with videos related to
Sort By:
Page
of 6
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 12, 1973
Propionic acid, an artefact which can leave methylmalonic acidemia undiscovered
M Duran, D Ketting, S K Wadman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 16, 1976
Glutaric aciduria type II: report on a previously undescribed metabolic disorder
H Przyrembel, U Wendel, K Becker, et al.
Journal of Chromatography
|
August 21, 1979
Urinary excretion of methylated purines in man and in the rat after the administration of theophylline
A H van Gennip, J Grift, E J van Bree-Blom, et al.
European Journal of Pediatrics
|
June 28, 1979
Two sisters with isovaleric acidaemia, multiple attacks of ketoacidosis and normal development
M Duran, F J van Sprang, J G Drewes, et al.
European Journal of Pediatrics
|
July 1, 1982
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs
F A Beemer, K Bartlett, M Duran, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 18, 1981
Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia
R Berger, G P Smit, S A Stoker-de Vries, et al.
The Journal of Pediatrics
|
January 1, 1979
Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase
R B Schutgens, H Heymans, A Ketel, et al.
The Journal of Pediatrics
|
December 1, 1979
3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency: postnatal management following prenatal diagnosis by analysis of maternal urine
M Duran, R B Schutgens, A Ketel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 15, 1985
Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids
M Duran, D Ketting, R van Vossen, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1982
Isovaleric acidaemia presenting with dwarfism, cataract and congenital abnormalities
M Duran, L Bruinvis, D Ketting, et al.
Page
of 6