C Bachmann|J P Colombo - JoVE Visualize

Showing results (21-30 of 246) with videos related to

Pageof 25

Sort By:

Klinische Padiatrie|March 1, 1990

[3-hydroxy-3-methylglutaraturia. Clinical aspects, follow-up and therapy in a young child]E Plöchl, C Bachmann, J P Colombo, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 1988

Determination of medium chain fatty acids in serumC 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 hyperammonemiaJ P Colombo, C Bachmann, H Cervantes, et al.

Pediatric Research|January 1, 1976

Gamma-glutamyltranspeptidase in the rat liver after portacaval shuntJ P Colombo, E Peheim, 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.

Journal of Inherited Metabolic Disease|January 1, 1988

N-acetylglutamate synthetase deficiency, a second patientC Bachmann, M Brandis, E Weissenbarth-Riedel, 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.

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.

European Journal of Pediatrics|March 1, 1991

N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxicationG Schubiger, C Bachmann, P Barben, et al.

Pageof 25

Showing results (21-30 of 246) with videos related to

Sort By:

Pageof 25

Klinische Padiatrie|March 1, 1990

[3-hydroxy-3-methylglutaraturia. Clinical aspects, follow-up and therapy in a young child]E Plöchl, C Bachmann, J P Colombo, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 1988

Determination of medium chain fatty acids in serumC 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 hyperammonemiaJ P Colombo, C Bachmann, H Cervantes, et al.

Pediatric Research|January 1, 1976

Gamma-glutamyltranspeptidase in the rat liver after portacaval shuntJ P Colombo, E Peheim, 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.

Journal of Inherited Metabolic Disease|January 1, 1988

N-acetylglutamate synthetase deficiency, a second patientC Bachmann, M Brandis, E Weissenbarth-Riedel, 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.

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.

European Journal of Pediatrics|March 1, 1991

N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxicationG Schubiger, C Bachmann, P Barben, et al.

Pageof 25