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J P Colombo

Showing results (101-110 of 159) with videos related to

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Das Medizinische Laboratorium|January 1, 1981
[Testing of 3 lipase determination methods]E Beck-Oostendorp, H P Köchli, P Degiampietro, et al.
British Journal of Clinical Pharmacology|December 1, 1979
The effect of enzyme induction on diazepam metabolism in manE E Ohnhaus, B K Park, J P Colombo, et al.
Human Mutation|January 1, 1996
Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphismsE O Oppliger Leibundgut, B Wermuth, J P Colombo, et al.
Enzyme|January 1, 1991
Direct and indirect mutation analyses in patients with ornithine transcarbamylase deficiencyS Liechti-Gallati, C Dionisi, C Bachmann, et al.
Pediatric Research|September 1, 1987
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplementC Dionisi Vici, C Bachmann, M Gambarara, et al.
Human Genetics|February 1, 1995
Ornithine transcarbamylase deficiency: new sites with increased probability of mutationE O Oppliger Leibundgut, S Liechti-Gallati, J P Colombo, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
N-acetylglutamate synthetase deficiency, a second patientC Bachmann, M Brandis, E Weissenbarth-Riedel, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1975
Unsuccessful trial of gene replacement in arginase deficiencyH G Terheggen, A Lowenthal, F Lavinha, et al.
European Journal of Pediatrics|June 1, 1990
Late-onset form of partial N-acetylglutamate synthetase deficiencyO N Elpeleg, J P Colombo, N Amir, et al.
European Journal of Pediatrics|January 1, 1994
Pitfalls in aminoacid and organic acid analysis: 3-hydroxypropionic aciduriaC Bachmann, O Boulat, B J Meyrat, et al.
Pageof 16

Showing results (101-110 of 159) with videos related to

Sort By:
Pageof 16
Das Medizinische Laboratorium|January 1, 1981
[Testing of 3 lipase determination methods]E Beck-Oostendorp, H P Köchli, P Degiampietro, et al.
British Journal of Clinical Pharmacology|December 1, 1979
The effect of enzyme induction on diazepam metabolism in manE E Ohnhaus, B K Park, J P Colombo, et al.
Human Mutation|January 1, 1996
Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphismsE O Oppliger Leibundgut, B Wermuth, J P Colombo, et al.
Enzyme|January 1, 1991
Direct and indirect mutation analyses in patients with ornithine transcarbamylase deficiencyS Liechti-Gallati, C Dionisi, C Bachmann, et al.
Pediatric Research|September 1, 1987
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplementC Dionisi Vici, C Bachmann, M Gambarara, et al.
Human Genetics|February 1, 1995
Ornithine transcarbamylase deficiency: new sites with increased probability of mutationE O Oppliger Leibundgut, S Liechti-Gallati, J P Colombo, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
N-acetylglutamate synthetase deficiency, a second patientC Bachmann, M Brandis, E Weissenbarth-Riedel, et al.
Zeitschrift Fur Kinderheilkunde|January 1, 1975
Unsuccessful trial of gene replacement in arginase deficiencyH G Terheggen, A Lowenthal, F Lavinha, et al.
European Journal of Pediatrics|June 1, 1990
Late-onset form of partial N-acetylglutamate synthetase deficiencyO N Elpeleg, J P Colombo, N Amir, et al.
European Journal of Pediatrics|January 1, 1994
Pitfalls in aminoacid and organic acid analysis: 3-hydroxypropionic aciduriaC Bachmann, O Boulat, B J Meyrat, et al.
Pageof 16