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C Jakobs

Showing results (291-300 of 417) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1992
Zellweger syndrome in a preterm, small for gestational age infantJ F Samsom, C Jakobs, J van de Klei-van Moorsel, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
4-Aminobutyrate aminotransferase (GABA-transaminase) deficiencyL K Medina-Kauwe, A J Tobin, L De Meirleir, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 3, 1998
No change in impaired endothelial function after long-term folic acid therapy of hyperhomocysteinaemia in haemodialysis patientsC van Guldener, M J Janssen, J Lambert, et al.
Fertility and Sterility|May 20, 1998
Postmenopausal oral 17beta-estradiol continuously combined with dydrogesterone reduces fasting serum homocysteine levelsV Mijatovic, P Kenemans, C Netelenbos, et al.
The Journal of Biological Chemistry|January 6, 1995
Molecular cloning of the mature NAD(+)-dependent succinic semialdehyde dehydrogenase from rat and human. cDNA isolation, evolutionary homology, and tissue expressionK L Chambliss, D L Caudle, D D Hinson, et al.
American Journal of Human Genetics|April 28, 2001
X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndromeG S Salomons, S J van Dooren, N M Verhoeven, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Formation of 2,3-pristenic acid and 3-hydroxypristanic acid from pristanic acid in human liverN M Verhoeven, D S Schor, G A Jansen, et al.
Human Molecular Genetics|April 18, 2000
Human phytanoyl-CoA hydroxylase: resolution of the gene structure and the molecular basis of Refsum's diseaseG A Jansen, E M Hogenhout, S Ferdinandusse, et al.
Journal of Vascular Surgery|December 1, 1994
Combined vitamin B6 plus folic acid therapy in young patients with arteriosclerosis and hyperhomocysteinemiaM van den Berg, D G Franken, G H Boers, et al.
Prenatal Diagnosis|October 30, 1998
Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuriaB Merinero, C Pérez-Cerdá, M J Garcia, et al.
Pageof 42

Showing results (291-300 of 417) with videos related to

Sort By:
Pageof 42
Journal of Inherited Metabolic Disease|January 1, 1992
Zellweger syndrome in a preterm, small for gestational age infantJ F Samsom, C Jakobs, J van de Klei-van Moorsel, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
4-Aminobutyrate aminotransferase (GABA-transaminase) deficiencyL K Medina-Kauwe, A J Tobin, L De Meirleir, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 3, 1998
No change in impaired endothelial function after long-term folic acid therapy of hyperhomocysteinaemia in haemodialysis patientsC van Guldener, M J Janssen, J Lambert, et al.
Fertility and Sterility|May 20, 1998
Postmenopausal oral 17beta-estradiol continuously combined with dydrogesterone reduces fasting serum homocysteine levelsV Mijatovic, P Kenemans, C Netelenbos, et al.
The Journal of Biological Chemistry|January 6, 1995
Molecular cloning of the mature NAD(+)-dependent succinic semialdehyde dehydrogenase from rat and human. cDNA isolation, evolutionary homology, and tissue expressionK L Chambliss, D L Caudle, D D Hinson, et al.
American Journal of Human Genetics|April 28, 2001
X-linked creatine-transporter gene (SLC6A8) defect: a new creatine-deficiency syndromeG S Salomons, S J van Dooren, N M Verhoeven, et al.
Journal of Inherited Metabolic Disease|July 1, 1997
Formation of 2,3-pristenic acid and 3-hydroxypristanic acid from pristanic acid in human liverN M Verhoeven, D S Schor, G A Jansen, et al.
Human Molecular Genetics|April 18, 2000
Human phytanoyl-CoA hydroxylase: resolution of the gene structure and the molecular basis of Refsum's diseaseG A Jansen, E M Hogenhout, S Ferdinandusse, et al.
Journal of Vascular Surgery|December 1, 1994
Combined vitamin B6 plus folic acid therapy in young patients with arteriosclerosis and hyperhomocysteinemiaM van den Berg, D G Franken, G H Boers, et al.
Prenatal Diagnosis|October 30, 1998
Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuriaB Merinero, C Pérez-Cerdá, M J Garcia, et al.
Pageof 42