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Journal of Inherited Metabolic Disease
|
January 1, 1986
Age-related differences in plasmalogen content of erythrocytes from patients with the cerebro-hepato-renal (Zellweger) syndrome: implications for postnatal detection of the disease
R J Wanders, Y R Purvis, H S Heymans, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1987
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency
A W Schram, S Goldfischer, C W van Roermund, et al.
European Journal of Biochemistry
|
August 1, 1985
The occurrence of two immunologically distinguishable beta-glucocerebrosidases in human spleen
J M Aerts, W E Donker-Koopman, M K van der Vliet, et al.
Enzyme
|
January 1, 1987
Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies
R B Schutgens, R J Wanders, A Nijenhuis, et al.
Human Genetics
|
January 1, 1983
Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies
R A Barneveld, W Keijzer, F P Tegelaers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1987
X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters
R J Wanders, C W van Roermund, M J van Wijland, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 15, 1987
Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders
R J Wanders, C W van Roermund, M J van Wijland, et al.
Page
of 18
Search research articles
Search
Showing results (171-180 of 177) with videos related to
Sort By:
Page
of 18
You have reached the last page of results.
This site can display upto 177 results.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Age-related differences in plasmalogen content of erythrocytes from patients with the cerebro-hepato-renal (Zellweger) syndrome: implications for postnatal detection of the disease
R J Wanders, Y R Purvis, H S Heymans, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1987
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency
A W Schram, S Goldfischer, C W van Roermund, et al.
European Journal of Biochemistry
|
August 1, 1985
The occurrence of two immunologically distinguishable beta-glucocerebrosidases in human spleen
J M Aerts, W E Donker-Koopman, M K van der Vliet, et al.
Enzyme
|
January 1, 1987
Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies
R B Schutgens, R J Wanders, A Nijenhuis, et al.
Human Genetics
|
January 1, 1983
Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies
R A Barneveld, W Keijzer, F P Tegelaers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1987
X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters
R J Wanders, C W van Roermund, M J van Wijland, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 15, 1987
Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders
R J Wanders, C W van Roermund, M J van Wijland, et al.
Page
of 18