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Biochimica Et Biophysica Acta
|
August 26, 1998
2,6-Dimethylheptanoyl-CoA is a specific substrate for long-chain acyl-CoA dehydrogenase (LCAD): evidence for a major role of LCAD in branched-chain fatty acid oxidation
R J Wanders, S Denis, J P Ruiter, et al.
Neurologia I Neurochirurgia Polska
|
February 15, 2000
[Adrenomyeloneuropathy: a form of X-linked adrenoleukodystrophy. Report of a family]
M Rzeski, W Kuran, H Mierzewska, et al.
Advances in Experimental Medicine and Biology
|
March 10, 2000
Carnitine biosynthesis. Purification of gamma-butyrobetaine hydroxylase from rat liver
F M Vaz, S van Gool, R Ofman, et al.
Pediatric Neurology
|
March 30, 2000
Muscular carnitine palmitoyltransferase II deficiency in infancy
H Hurvitz, A Klar, I Korn-Lubetzki, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Mitochondropathy presenting with non-ketotic hypoglycaemia as 3-hydroxydicarboxylic aciduria
E Mayatepek, R J Wanders, M Becker, et al.
Biochemical and Biophysical Research Communications
|
October 1, 1998
Plasmalogen phospholipids are involved in HDL-mediated cholesterol efflux: insights from investigations with plasmalogen-deficient cells
H Mandel, R Sharf, M Berant, et al.
Biochemical and Biophysical Research Communications
|
October 1, 1998
Carnitine biosynthesis: identification of the cDNA encoding human gamma-butyrobetaine hydroxylase
F M Vaz, S van Gool, R Ofman, et al.
Biochemical and Biophysical Research Communications
|
June 9, 1997
Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein
E G van Grunsven, C W van Roermund, S Denis, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Identification of pristanoyl-CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: implications for Zellweger syndrome
R J Wanders, C W van Roermund, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Bile acids in amniotic fluid: promising metabolites for the prenatal diagnosis of peroxisomal disorders
F Stellaard, W J Kleijer, R J Wanders, et al.
Page
of 50
Search research articles
Search
Showing results (111-120 of 497) with videos related to
Sort By:
Page
of 50
Biochimica Et Biophysica Acta
|
August 26, 1998
2,6-Dimethylheptanoyl-CoA is a specific substrate for long-chain acyl-CoA dehydrogenase (LCAD): evidence for a major role of LCAD in branched-chain fatty acid oxidation
R J Wanders, S Denis, J P Ruiter, et al.
Neurologia I Neurochirurgia Polska
|
February 15, 2000
[Adrenomyeloneuropathy: a form of X-linked adrenoleukodystrophy. Report of a family]
M Rzeski, W Kuran, H Mierzewska, et al.
Advances in Experimental Medicine and Biology
|
March 10, 2000
Carnitine biosynthesis. Purification of gamma-butyrobetaine hydroxylase from rat liver
F M Vaz, S van Gool, R Ofman, et al.
Pediatric Neurology
|
March 30, 2000
Muscular carnitine palmitoyltransferase II deficiency in infancy
H Hurvitz, A Klar, I Korn-Lubetzki, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Mitochondropathy presenting with non-ketotic hypoglycaemia as 3-hydroxydicarboxylic aciduria
E Mayatepek, R J Wanders, M Becker, et al.
Biochemical and Biophysical Research Communications
|
October 1, 1998
Plasmalogen phospholipids are involved in HDL-mediated cholesterol efflux: insights from investigations with plasmalogen-deficient cells
H Mandel, R Sharf, M Berant, et al.
Biochemical and Biophysical Research Communications
|
October 1, 1998
Carnitine biosynthesis: identification of the cDNA encoding human gamma-butyrobetaine hydroxylase
F M Vaz, S van Gool, R Ofman, et al.
Biochemical and Biophysical Research Communications
|
June 9, 1997
Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein
E G van Grunsven, C W van Roermund, S Denis, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Identification of pristanoyl-CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: implications for Zellweger syndrome
R J Wanders, C W van Roermund, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Bile acids in amniotic fluid: promising metabolites for the prenatal diagnosis of peroxisomal disorders
F Stellaard, W J Kleijer, R J Wanders, et al.
Page
of 50