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C Jakobs

Showing results (231-240 of 417) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|January 27, 2005
Oral estradiol decreases plasma homocysteine, vitamin B6, and albumin in postmenopausal women but does not change the whole-body homocysteine remethylation and transmethylation fluxR G V Smolders, K de Meer, P Kenemans, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Kinetic characterization of human hydroxyacid-oxoacid transhydrogenase: relevance to D-2-hydroxyglutaric and gamma-hydroxybutyric aciduriasE A Struys, N M Verhoeven, H J Ten Brink, et al.
European Journal of Pediatrics|February 1, 1990
A new case of hyperargininaemia: neurological and biochemical findings prior to and during dietary treatmentM Brockstedt, L M Smit, A J de Grauw, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Pearson syndrome: altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacitiesA Ribes, E Riudor, R Valcárel, et al.
The American Journal of Physiology|March 1, 1996
Leucine and glucose kinetics during growth hormone treatment in intrauterine growth-retarded preterm infantsL Van Toledo-Eppinga, M C Houdijk, H A Delemarre-Van De Waal, et al.
Journal of Medical Genetics|June 3, 2004
5,10-methylenetetrahydrofolate reductase (MTHFR) 677C-->T and 1298A-->C mutations are associated with DNA hypomethylationR Castro, I Rivera, P Ravasco, et al.
Cardiovascular Research|March 17, 2004
Inhibition of the pentose phosphate pathway decreases ischemia-reperfusion-induced creatine kinase release in the heartC J Zuurbier, O Eerbeek, P T Goedhart, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|October 12, 2004
Hormone replacement influences homocysteine levels in the methionine-loading test: a randomized placebo controlled trial in postmenopausal womenR G V Smolders, K de Meer, P Kenemans, et al.
Neuropediatrics|January 22, 2003
Congenital creatine transporter deficiencyT J deGrauw, G S Salomons, K M Cecil, et al.
Prenatal Diagnosis|August 1, 1995
Molecular prenatal diagnosis of 3-hydroxy-3-methylglutaryl CoA lyase deficiencyG A Mitchell, C Jakobs, K M Gibson, et al.
Pageof 42

Showing results (231-240 of 417) with videos related to

Sort By:
Pageof 42
The Journal of Clinical Endocrinology and Metabolism|January 27, 2005
Oral estradiol decreases plasma homocysteine, vitamin B6, and albumin in postmenopausal women but does not change the whole-body homocysteine remethylation and transmethylation fluxR G V Smolders, K de Meer, P Kenemans, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Kinetic characterization of human hydroxyacid-oxoacid transhydrogenase: relevance to D-2-hydroxyglutaric and gamma-hydroxybutyric aciduriasE A Struys, N M Verhoeven, H J Ten Brink, et al.
European Journal of Pediatrics|February 1, 1990
A new case of hyperargininaemia: neurological and biochemical findings prior to and during dietary treatmentM Brockstedt, L M Smit, A J de Grauw, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Pearson syndrome: altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacitiesA Ribes, E Riudor, R Valcárel, et al.
The American Journal of Physiology|March 1, 1996
Leucine and glucose kinetics during growth hormone treatment in intrauterine growth-retarded preterm infantsL Van Toledo-Eppinga, M C Houdijk, H A Delemarre-Van De Waal, et al.
Journal of Medical Genetics|June 3, 2004
5,10-methylenetetrahydrofolate reductase (MTHFR) 677C-->T and 1298A-->C mutations are associated with DNA hypomethylationR Castro, I Rivera, P Ravasco, et al.
Cardiovascular Research|March 17, 2004
Inhibition of the pentose phosphate pathway decreases ischemia-reperfusion-induced creatine kinase release in the heartC J Zuurbier, O Eerbeek, P T Goedhart, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|October 12, 2004
Hormone replacement influences homocysteine levels in the methionine-loading test: a randomized placebo controlled trial in postmenopausal womenR G V Smolders, K de Meer, P Kenemans, et al.
Neuropediatrics|January 22, 2003
Congenital creatine transporter deficiencyT J deGrauw, G S Salomons, K M Cecil, et al.
Prenatal Diagnosis|August 1, 1995
Molecular prenatal diagnosis of 3-hydroxy-3-methylglutaryl CoA lyase deficiencyG A Mitchell, C Jakobs, K M Gibson, et al.
Pageof 42