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R J Wanders

Showing results (91-100 of 497) with videos related to

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The New England Journal of Medicine|July 10, 1997
Phytanoyl-coenzyme A hydroxylase deficiency -- the enzyme defect in Refsum's diseaseG A Jansen, R J Wanders, P A Watkins, et al.
Biochemical and Biophysical Research Communications|July 30, 1997
Sterol carrier protein X (SCPx) is a peroxisomal branched-chain beta-ketothiolase specifically reacting with 3-oxo-pristanoyl-CoA: a new, unique role for SCPx in branched-chain fatty acid metabolism in peroxisomesR J Wanders, S Denis, F Wouters, et al.
European Journal of Pediatrics|February 1, 1992
Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patientsA C Theil, R B Schutgens, R J Wanders, et al.
Dermatology (Basel, Switzerland)|November 13, 1999
Incomplete Sjögren-Larsson syndrome in two Japanese siblings?M A Willemsen, J J Rotteveel, P M Steijlen, et al.
American Journal of Medical Genetics|March 10, 2001
No cholesterol metabolism anomalies detectable in infants with hypertrophic pyloric stenosisR C Hennekam, H R Waterham, R J Wanders, et al.
Cell Biophysics|December 1, 1987
Thermodynamics of the control of metabolismH V Westerhoff, P J Plomp, A K Groen, et al.
Biochemical and Biophysical Research Communications|October 16, 1989
L-pipecolate oxidase: a distinct peroxisomal enzyme in manR J Wanders, G J Romeyn, R B Schutgens, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapyB M van Geel, J Assies, R J Wanders, et al.
Biochimica Et Biophysica Acta|February 10, 1994
Beta-oxidation of fatty acids in cultured human skin fibroblasts devoid of the capacity for oxidative phosphorylationB S Jakobs, C van den Bogert, G Dacremont, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Disorders of peroxisome biogenesis: complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency)R J Wanders, P A Mooijer, C Dekker, et al.
Pageof 50

Showing results (91-100 of 497) with videos related to

Sort By:
Pageof 50
The New England Journal of Medicine|July 10, 1997
Phytanoyl-coenzyme A hydroxylase deficiency -- the enzyme defect in Refsum's diseaseG A Jansen, R J Wanders, P A Watkins, et al.
Biochemical and Biophysical Research Communications|July 30, 1997
Sterol carrier protein X (SCPx) is a peroxisomal branched-chain beta-ketothiolase specifically reacting with 3-oxo-pristanoyl-CoA: a new, unique role for SCPx in branched-chain fatty acid metabolism in peroxisomesR J Wanders, S Denis, F Wouters, et al.
European Journal of Pediatrics|February 1, 1992
Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patientsA C Theil, R B Schutgens, R J Wanders, et al.
Dermatology (Basel, Switzerland)|November 13, 1999
Incomplete Sjögren-Larsson syndrome in two Japanese siblings?M A Willemsen, J J Rotteveel, P M Steijlen, et al.
American Journal of Medical Genetics|March 10, 2001
No cholesterol metabolism anomalies detectable in infants with hypertrophic pyloric stenosisR C Hennekam, H R Waterham, R J Wanders, et al.
Cell Biophysics|December 1, 1987
Thermodynamics of the control of metabolismH V Westerhoff, P J Plomp, A K Groen, et al.
Biochemical and Biophysical Research Communications|October 16, 1989
L-pipecolate oxidase: a distinct peroxisomal enzyme in manR J Wanders, G J Romeyn, R B Schutgens, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapyB M van Geel, J Assies, R J Wanders, et al.
Biochimica Et Biophysica Acta|February 10, 1994
Beta-oxidation of fatty acids in cultured human skin fibroblasts devoid of the capacity for oxidative phosphorylationB S Jakobs, C van den Bogert, G Dacremont, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Disorders of peroxisome biogenesis: complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency)R J Wanders, P A Mooijer, C Dekker, et al.
Pageof 50