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M Duran

Showing results (321-330 of 646) with videos related to

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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 oxidationE 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. coliP Vreken, A B van Kuilenburg, R Meinsma, et al.
Current Molecular Medicine|March 10, 2018
Graphene Oxide as Scaffolds for Stem Cells: An OverviewM 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 sibsF 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 tyrosinemiaR 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 metabolismM 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 lyaseR B Schutgens, H Heymans, A Ketel, et al.
Lancet (London, England)|September 29, 1990
DihydropyrimidinuriaM 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 angiographyM Duran, S O Schoenberg, W T C Yuh, et al.
Pageof 65

Showing results (321-330 of 646) with videos related to

Sort By:
Pageof 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 oxidationE 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. coliP Vreken, A B van Kuilenburg, R Meinsma, et al.
Current Molecular Medicine|March 10, 2018
Graphene Oxide as Scaffolds for Stem Cells: An OverviewM 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 sibsF 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 tyrosinemiaR 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 metabolismM 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 lyaseR B Schutgens, H Heymans, A Ketel, et al.
Lancet (London, England)|September 29, 1990
DihydropyrimidinuriaM 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 angiographyM Duran, S O Schoenberg, W T C Yuh, et al.
Pageof 65