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Archives of Disease in Childhood
|
January 1, 1975
Familial hyperargininaemia
H G Terheggen, A Lowenthal, F Lavinha, et al.
Enzyme
|
January 1, 1983
Isoenzyme pattern and immunological properties of arginase in normal and hyperargininemia fibroblasts
L Konarska, U Wiesmann, R von Fellenberg, et al.
Metabolism: Clinical and Experimental
|
January 1, 1973
Synthesis of glucose in human thrombocytes
N Nakamura, K A Zuppinger, J P Colombo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 15, 1974
A new accelerator for the determination of total bilirubin in plasma
J P Colombo, E Peheim, S Kyburz, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie
|
June 1, 1985
Human salivary arginase and its deficiency in argininaemia
L Konarska, L Tomaszewski, J P Colombo, et al.
Clinical Chemistry
|
February 1, 1992
Increased plasma amylase in the family of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency
E Plöchl, J P Colombo, B Wermuth, et al.
Journal of Inherited Metabolic Disease
|
January 14, 1998
N-Acetylglutamate synthetase deficiency responding to carbamylglutamate
J Hinnie, J P Colombo, B Wermuth, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 15, 1988
Determination of medium chain fatty acids in serum
C Dionisi Vici, C Bachmann, M Gradwoht, et al.
Pediatric Research
|
June 1, 1996
Tyrosine uptake and regional brain monoamine metabolites in a rat model resembling congenital hyperammonemia
J P Colombo, C Bachmann, H Cervantes, et al.
Pediatric Research
|
January 1, 1976
Gamma-glutamyltranspeptidase in the rat liver after portacaval shunt
J P Colombo, E Peheim, C Bachmann, et al.
Page
of 16
Search research articles
Search
Showing results (81-90 of 159) with videos related to
Sort By:
Page
of 16
Archives of Disease in Childhood
|
January 1, 1975
Familial hyperargininaemia
H G Terheggen, A Lowenthal, F Lavinha, et al.
Enzyme
|
January 1, 1983
Isoenzyme pattern and immunological properties of arginase in normal and hyperargininemia fibroblasts
L Konarska, U Wiesmann, R von Fellenberg, et al.
Metabolism: Clinical and Experimental
|
January 1, 1973
Synthesis of glucose in human thrombocytes
N Nakamura, K A Zuppinger, J P Colombo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 15, 1974
A new accelerator for the determination of total bilirubin in plasma
J P Colombo, E Peheim, S Kyburz, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie
|
June 1, 1985
Human salivary arginase and its deficiency in argininaemia
L Konarska, L Tomaszewski, J P Colombo, et al.
Clinical Chemistry
|
February 1, 1992
Increased plasma amylase in the family of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency
E Plöchl, J P Colombo, B Wermuth, et al.
Journal of Inherited Metabolic Disease
|
January 14, 1998
N-Acetylglutamate synthetase deficiency responding to carbamylglutamate
J Hinnie, J P Colombo, B Wermuth, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 15, 1988
Determination of medium chain fatty acids in serum
C Dionisi Vici, C Bachmann, M Gradwoht, et al.
Pediatric Research
|
June 1, 1996
Tyrosine uptake and regional brain monoamine metabolites in a rat model resembling congenital hyperammonemia
J P Colombo, C Bachmann, H Cervantes, et al.
Pediatric Research
|
January 1, 1976
Gamma-glutamyltranspeptidase in the rat liver after portacaval shunt
J P Colombo, E Peheim, C Bachmann, et al.
Page
of 16