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Journal of Inherited Metabolic Disease
|
January 1, 1992
Unusual clinical presentation in two boys with cytochrome c oxidase deficiency
M Hrebícek, J Zeman, B Petrák, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
March 31, 1990
[Zellweger syndrome and other peroxisomal disorders: I. Clinical characteristics of a recently discovered group of diseases]
H S Heymans, R J Wanders, R B Schutgens, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: different clinical expression in three unrelated patients
R J Wanders, L Ijlst, M Duran, et al.
Biochemical and Biophysical Research Communications
|
October 30, 1990
Identification of pristanoyl-CoA oxidase activity in human liver and its deficiency in the Zellweger syndrome
R J Wanders, H J ten Brink, C W van Roermund, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1986
Regulation of mitochondrial respiration in liver
A J Verhoeven, C W van Roermund, P J Plomp, et al.
Pediatric Research
|
December 1, 1990
Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhood
F Rocchiccioli, R J Wanders, P Aubourg, et al.
European Journal of Pediatrics
|
April 1, 1989
Very long fatty acids in amniotic fluid from a fetus affected with Zellweger syndrome
C Jakobs, H ten Brink, R M Kok, et al.
Biochemical and Biophysical Research Communications
|
November 16, 1992
Human trifunctional protein deficiency: a new disorder of mitochondrial fatty acid beta-oxidation
R J Wanders, L IJlst, F Poggi, et al.
Journal of Lipid Research
|
October 1, 1992
Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders
H J ten Brink, D S Schor, R M Kok, et al.
The Journal of Pediatrics
|
February 5, 2000
Defective inactivation of leukotriene B4 in patients with Sjögren-Larsson syndrome
M A Willemsen, J G de Jong, P H van Domburg, et al.
Page
of 50
Search research articles
Search
Showing results (291-300 of 497) with videos related to
Sort By:
Page
of 50
Journal of Inherited Metabolic Disease
|
January 1, 1992
Unusual clinical presentation in two boys with cytochrome c oxidase deficiency
M Hrebícek, J Zeman, B Petrák, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
March 31, 1990
[Zellweger syndrome and other peroxisomal disorders: I. Clinical characteristics of a recently discovered group of diseases]
H S Heymans, R J Wanders, R B Schutgens, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: different clinical expression in three unrelated patients
R J Wanders, L Ijlst, M Duran, et al.
Biochemical and Biophysical Research Communications
|
October 30, 1990
Identification of pristanoyl-CoA oxidase activity in human liver and its deficiency in the Zellweger syndrome
R J Wanders, H J ten Brink, C W van Roermund, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1986
Regulation of mitochondrial respiration in liver
A J Verhoeven, C W van Roermund, P J Plomp, et al.
Pediatric Research
|
December 1, 1990
Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhood
F Rocchiccioli, R J Wanders, P Aubourg, et al.
European Journal of Pediatrics
|
April 1, 1989
Very long fatty acids in amniotic fluid from a fetus affected with Zellweger syndrome
C Jakobs, H ten Brink, R M Kok, et al.
Biochemical and Biophysical Research Communications
|
November 16, 1992
Human trifunctional protein deficiency: a new disorder of mitochondrial fatty acid beta-oxidation
R J Wanders, L IJlst, F Poggi, et al.
Journal of Lipid Research
|
October 1, 1992
Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders
H J ten Brink, D S Schor, R M Kok, et al.
The Journal of Pediatrics
|
February 5, 2000
Defective inactivation of leukotriene B4 in patients with Sjögren-Larsson syndrome
M A Willemsen, J G de Jong, P H van Domburg, et al.
Page
of 50