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Progress in Clinical and Biological Research
|
January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidation
E Schmidt-Sommerfeld, D Penn, M Duran, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Dihydropyrimidine dehydrogenase deficiency: a novel mutation and expression of missense mutations in E. coli
P Vreken, A B van Kuilenburg, R Meinsma, et al.
Current Molecular Medicine
|
March 10, 2018
Graphene Oxide as Scaffolds for Stem Cells: An Overview
M Duran, A C M Luzo, J G de Souza, 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.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism
M Duran, P Rovers, P K de Bree, 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.
Lancet (London, England)
|
September 29, 1990
Dihydropyrimidinuria
M Duran, P Rovers, P K de Bree, et al.
International Journal of Clinical Practice
|
January 16, 2009
Prognostic factors in the diagnostic work-up of cancer patients in an internal medicine department: does age matter?
E Domingo, J M Suriñach, J Murillo, et al.
European Radiology
|
November 20, 2002
Cerebral arteriovenous malformations: morphologic evaluation by ultrashort 3D gadolinium-enhanced MR angiography
M Duran, S O Schoenberg, W T C Yuh, et al.
Page
of 65
Search research articles
Search
Showing results (321-330 of 646) with videos related to
Sort By:
Page
of 65
Progress in Clinical and Biological Research
|
January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidation
E Schmidt-Sommerfeld, D Penn, M Duran, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Dihydropyrimidine dehydrogenase deficiency: a novel mutation and expression of missense mutations in E. coli
P Vreken, A B van Kuilenburg, R Meinsma, et al.
Current Molecular Medicine
|
March 10, 2018
Graphene Oxide as Scaffolds for Stem Cells: An Overview
M Duran, A C M Luzo, J G de Souza, 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.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism
M Duran, P Rovers, P K de Bree, 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.
Lancet (London, England)
|
September 29, 1990
Dihydropyrimidinuria
M Duran, P Rovers, P K de Bree, et al.
International Journal of Clinical Practice
|
January 16, 2009
Prognostic factors in the diagnostic work-up of cancer patients in an internal medicine department: does age matter?
E Domingo, J M Suriñach, J Murillo, et al.
European Radiology
|
November 20, 2002
Cerebral arteriovenous malformations: morphologic evaluation by ultrashort 3D gadolinium-enhanced MR angiography
M Duran, S O Schoenberg, W T C Yuh, et al.
Page
of 65