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Tijdschrift Voor Kindergeneeskunde
|
December 1, 1984
[Diagnosis of hereditary metabolic diseases using chromatographic technics]
H A Veder, R B Schutgens
Nederlands Tijdschrift Voor Geneeskunde
|
June 7, 1975
[Letter: Zonular cataract in an infant]
R B Schutgens, F A Beener
Nederlands Tijdschrift Voor Geneeskunde
|
December 28, 1974
[Fermentation diarrhea due to deficiency of sucrase and isomaltase activity of the intestinal parietal cells]
N Ceelie, R B Schutgens, M Sinaasappel
Journal of Inherited Metabolic Disease
|
January 1, 1994
Peroxisomal functions in mulibrey nanism
R B Schutgens, M Ryynänen, R J Wanders
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1978
An improved quantitative assay of galactose-1-phosphate uridyltransferase activity in erythrocytes based on the determination of glucose 1-phosphate generation
R B Schutgens, W J Berntssen, L Pool
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 15, 1987
Deficient cholesterol side chain oxidation in patients without peroxisomes (Zellweger syndrome): evidence for the involvement of peroxisomes in bile acid synthesis in man
R J Wanders, R B Schutgens, H S Heymans
Journal of Inherited Metabolic Disease
|
January 1, 1988
Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria via enzyme activity measurements in chorionic villi, chorionic villous fibroblasts or amniocytes using a simple spectrophotometric method
R J Wanders, R B Schutgens, B H Zoeters
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 15, 1988
3-Hydroxy-3-methylglutaryl-CoA lyase in human skin fibroblasts: study of its properties and deficient activity in 3-hydroxy-3-methylglutaric aciduria patients using a simple spectrophotometric method
R J Wanders, R B Schutgens, P H Zoeters
Journal of Inherited Metabolic Disease
|
January 1, 1985
Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liver
R J Wanders, R B Schutgens, J M Tager
Journal of Neuropathology and Experimental Neurology
|
September 1, 1995
Peroxisomal disorders: a review
R J Wanders, R B Schutgens, P G Barth
Page
of 20
Search research articles
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Showing results (1-10 of 200) with videos related to
Sort By:
Page
of 20
Tijdschrift Voor Kindergeneeskunde
|
December 1, 1984
[Diagnosis of hereditary metabolic diseases using chromatographic technics]
H A Veder, R B Schutgens
Nederlands Tijdschrift Voor Geneeskunde
|
June 7, 1975
[Letter: Zonular cataract in an infant]
R B Schutgens, F A Beener
Nederlands Tijdschrift Voor Geneeskunde
|
December 28, 1974
[Fermentation diarrhea due to deficiency of sucrase and isomaltase activity of the intestinal parietal cells]
N Ceelie, R B Schutgens, M Sinaasappel
Journal of Inherited Metabolic Disease
|
January 1, 1994
Peroxisomal functions in mulibrey nanism
R B Schutgens, M Ryynänen, R J Wanders
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1978
An improved quantitative assay of galactose-1-phosphate uridyltransferase activity in erythrocytes based on the determination of glucose 1-phosphate generation
R B Schutgens, W J Berntssen, L Pool
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 15, 1987
Deficient cholesterol side chain oxidation in patients without peroxisomes (Zellweger syndrome): evidence for the involvement of peroxisomes in bile acid synthesis in man
R J Wanders, R B Schutgens, H S Heymans
Journal of Inherited Metabolic Disease
|
January 1, 1988
Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria via enzyme activity measurements in chorionic villi, chorionic villous fibroblasts or amniocytes using a simple spectrophotometric method
R J Wanders, R B Schutgens, B H Zoeters
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 15, 1988
3-Hydroxy-3-methylglutaryl-CoA lyase in human skin fibroblasts: study of its properties and deficient activity in 3-hydroxy-3-methylglutaric aciduria patients using a simple spectrophotometric method
R J Wanders, R B Schutgens, P H Zoeters
Journal of Inherited Metabolic Disease
|
January 1, 1985
Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liver
R J Wanders, R B Schutgens, J M Tager
Journal of Neuropathology and Experimental Neurology
|
September 1, 1995
Peroxisomal disorders: a review
R J Wanders, R B Schutgens, P G Barth
Page
of 20