Search research articles
Contact Us
Filters
Showing results (191-200 of 497) with videos related to
Page
of 50
Sort By:
Journal of Inherited Metabolic Disease
|
November 5, 1997
A new peroxisomal beta-oxidation disorder in twin neonates: defective oxidation of both cerotic and pristanic acids
E Christensen, S A Pedersen, H Leth, et al.
Clinical Chemistry
|
August 1, 1993
Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata
R B Schutgens, I W Bouman, A A Nijenhuis, et al.
Archives of Disease in Childhood
|
March 1, 1993
Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency
D G Barr, J M Kirk, M al Howasi, et al.
Journal of Inherited Metabolic Disease
|
November 20, 1998
The metabolism of phytanic acid and pristanic acid in man: a review
N M Verhoeven, R J Wanders, B T Poll-The, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Identification of the newly discovered 58 kDa peroxisomal thiolase SCPx as the main thiolase involved in both pristanic acid and trihydroxycholestanoic acid oxidation: implications for peroxisomal beta-oxidation disorders
R J Wanders, S Denis, E van Berkel, et al.
Human Mutation
|
June 30, 2000
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basis
C M Aalfs, G B Salieb-Beugelaar, R J Wanders, et al.
European Journal of Pediatrics
|
February 1, 1986
Peroxisomal disorders: a newly recognised group of genetic diseases
R B Schutgens, H S Heymans, R J Wanders, et al.
The Journal of Pediatrics
|
March 4, 2000
Carbohydrate-deficient glycoprotein syndrome type 1a: a variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbances
C H van Ommen, M Peters, P G Barth, et al.
FEBS Letters
|
July 14, 1998
Involvement of microsomal fatty aldehyde dehydrogenase in the alpha-oxidation of phytanic acid
N M Verhoeven, C Jakobs, G Carney, et al.
FEBS Letters
|
January 7, 1985
The phosphate potential maintained by mitochondria in State 4 is proportional to the proton-motive force
H Woelders, W J van der Zande, A M Colen, et al.
Page
of 50
Search research articles
Search
Showing results (191-200 of 497) with videos related to
Sort By:
Page
of 50
Journal of Inherited Metabolic Disease
|
November 5, 1997
A new peroxisomal beta-oxidation disorder in twin neonates: defective oxidation of both cerotic and pristanic acids
E Christensen, S A Pedersen, H Leth, et al.
Clinical Chemistry
|
August 1, 1993
Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata
R B Schutgens, I W Bouman, A A Nijenhuis, et al.
Archives of Disease in Childhood
|
March 1, 1993
Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency
D G Barr, J M Kirk, M al Howasi, et al.
Journal of Inherited Metabolic Disease
|
November 20, 1998
The metabolism of phytanic acid and pristanic acid in man: a review
N M Verhoeven, R J Wanders, B T Poll-The, et al.
Journal of Inherited Metabolic Disease
|
August 1, 1998
Identification of the newly discovered 58 kDa peroxisomal thiolase SCPx as the main thiolase involved in both pristanic acid and trihydroxycholestanoic acid oxidation: implications for peroxisomal beta-oxidation disorders
R J Wanders, S Denis, E van Berkel, et al.
Human Mutation
|
June 30, 2000
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: determination of the molecular basis
C M Aalfs, G B Salieb-Beugelaar, R J Wanders, et al.
European Journal of Pediatrics
|
February 1, 1986
Peroxisomal disorders: a newly recognised group of genetic diseases
R B Schutgens, H S Heymans, R J Wanders, et al.
The Journal of Pediatrics
|
March 4, 2000
Carbohydrate-deficient glycoprotein syndrome type 1a: a variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbances
C H van Ommen, M Peters, P G Barth, et al.
FEBS Letters
|
July 14, 1998
Involvement of microsomal fatty aldehyde dehydrogenase in the alpha-oxidation of phytanic acid
N M Verhoeven, C Jakobs, G Carney, et al.
FEBS Letters
|
January 7, 1985
The phosphate potential maintained by mitochondria in State 4 is proportional to the proton-motive force
H Woelders, W J van der Zande, A M Colen, et al.
Page
of 50