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M Duran

Showing results (241-250 of 646) with videos related to

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Pediatric Nephrology (Berlin, Germany)|November 30, 2000
Oral L-carnitine does not decrease erythropoietin requirement in pediatric dialysisM R Lilien, M Duran, J M Quak, et al.
Catheterization and Cardiovascular Diagnosis|October 1, 1990
Regression of infundibular pulmonary stenosis after successful balloon pulmonary valvuloplasty in adultsM E Fawzy, O Galal, B Dunn, et al.
European Journal of Pediatrics|December 1, 1988
Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiencyW Endres, Y S Shin, R Günther, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research|March 25, 2008
Odor control during post-digestion processing of biosolids through bioaugmentation of anaerobic digestionN Tepe, D Yurtsever, R J Mehta, et al.
Pediatrics|September 2, 2000
Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatmentJ G Huijmans, M Duran, J B de Klerk, et al.
The Annals of Thoracic Surgery|August 1, 1995
Autologous glutaraldehyde-treated pericardial valved conduit: an experimental studyM N Kumar, G Prabakar, N Kumar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1978
Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefactsM Duran, D Ketting, S K Wadman, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Medium-chain triglyceride loading has no diagnostic power in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyC G Costa, I T de Almeida, C Jakobs, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 31, 1991
Gas chromatography method for the separation of amino acids enantiomers in plasma and urine. Application in a case of short bowel syndromeD Ketting, S K Wadman, L J Spaapen, et al.
The Journal of Clinical Investigation|April 1, 1986
Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduriaK Narisawa, K M Gibson, L Sweetman, et al.
Pageof 65

Showing results (241-250 of 646) with videos related to

Sort By:
Pageof 65
Pediatric Nephrology (Berlin, Germany)|November 30, 2000
Oral L-carnitine does not decrease erythropoietin requirement in pediatric dialysisM R Lilien, M Duran, J M Quak, et al.
Catheterization and Cardiovascular Diagnosis|October 1, 1990
Regression of infundibular pulmonary stenosis after successful balloon pulmonary valvuloplasty in adultsM E Fawzy, O Galal, B Dunn, et al.
European Journal of Pediatrics|December 1, 1988
Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiencyW Endres, Y S Shin, R Günther, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research|March 25, 2008
Odor control during post-digestion processing of biosolids through bioaugmentation of anaerobic digestionN Tepe, D Yurtsever, R J Mehta, et al.
Pediatrics|September 2, 2000
Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatmentJ G Huijmans, M Duran, J B de Klerk, et al.
The Annals of Thoracic Surgery|August 1, 1995
Autologous glutaraldehyde-treated pericardial valved conduit: an experimental studyM N Kumar, G Prabakar, N Kumar, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1978
Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefactsM Duran, D Ketting, S K Wadman, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Medium-chain triglyceride loading has no diagnostic power in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyC G Costa, I T de Almeida, C Jakobs, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 31, 1991
Gas chromatography method for the separation of amino acids enantiomers in plasma and urine. Application in a case of short bowel syndromeD Ketting, S K Wadman, L J Spaapen, et al.
The Journal of Clinical Investigation|April 1, 1986
Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduriaK Narisawa, K M Gibson, L Sweetman, et al.
Pageof 65