Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Bachmann

Showing results (51-60 of 233) with videos related to

Pageof 24
Sort By:
Lancet (London, England)|December 1, 2001
Treatment of neonatal hyperammonaemiaJ O Sass, W Sperl, C Bachmann
Enzyme|January 1, 1976
Congenital methylmalonic acidemia: a variant of the B12 'non-responsive' form with evidence for reduced affinity of methylmalonyl-CoA mutase for its B12-coenzymeE R Baumgartner, C Bachmann, H Wick
Advances in Experimental Medicine and Biology|January 1, 1982
N-acetylglutamate synthetase (NAGS) deficiency: diagnosis, clinical observations and treatmentC Bachmann, J P Colombo, K Jaggi
Journal of Inherited Metabolic Disease|January 1, 1987
Ornithine transcarbamylase variant in a male patientS Stöckler, F Grossschädl, C Bachmann, et al.
Schweizerische Medizinische Wochenschrift|December 6, 1980
[The therapeutic efficacy of bezafibrate in hyperlipoproteinemias of various types]G Noseda, C Fragiacomo, P Weidmann, et al.
Acta Psychiatrica Scandinavica|September 15, 2016
Use of psychotropic drugs in patients with autism spectrum disorders: a systematic reviewK Jobski, J Höfer, F Hoffmann, et al.
Epilepsia|August 1, 1995
Reduction of plasma alanine aminotransferase during vigabatrin treatmentG B Foletti, M C Delisle, C Bachmann
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|September 1, 1993
Plasma carnitines: reference values in an ambulatory populationO Boulat, B Janin, P Francioli, et al.
European Journal of Pediatrics|May 1, 1988
DNA analysis of ornithine transcarbamylase deficiencyU Wendel, E Wilichowski, J Schmidtke, et al.
Helvetica Paediatrica Acta|June 1, 1989
[Carbamyl phosphate synthase deficiency: clinical symptoms, diagnosis and dietary-medicamentous treatment in the neonatal period and infancy]H Hochreutener, J Issakainen, C Bachmann, et al.
Pageof 24

Showing results (51-60 of 233) with videos related to

Sort By:
Pageof 24
Lancet (London, England)|December 1, 2001
Treatment of neonatal hyperammonaemiaJ O Sass, W Sperl, C Bachmann
Enzyme|January 1, 1976
Congenital methylmalonic acidemia: a variant of the B12 'non-responsive' form with evidence for reduced affinity of methylmalonyl-CoA mutase for its B12-coenzymeE R Baumgartner, C Bachmann, H Wick
Advances in Experimental Medicine and Biology|January 1, 1982
N-acetylglutamate synthetase (NAGS) deficiency: diagnosis, clinical observations and treatmentC Bachmann, J P Colombo, K Jaggi
Journal of Inherited Metabolic Disease|January 1, 1987
Ornithine transcarbamylase variant in a male patientS Stöckler, F Grossschädl, C Bachmann, et al.
Schweizerische Medizinische Wochenschrift|December 6, 1980
[The therapeutic efficacy of bezafibrate in hyperlipoproteinemias of various types]G Noseda, C Fragiacomo, P Weidmann, et al.
Acta Psychiatrica Scandinavica|September 15, 2016
Use of psychotropic drugs in patients with autism spectrum disorders: a systematic reviewK Jobski, J Höfer, F Hoffmann, et al.
Epilepsia|August 1, 1995
Reduction of plasma alanine aminotransferase during vigabatrin treatmentG B Foletti, M C Delisle, C Bachmann
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|September 1, 1993
Plasma carnitines: reference values in an ambulatory populationO Boulat, B Janin, P Francioli, et al.
European Journal of Pediatrics|May 1, 1988
DNA analysis of ornithine transcarbamylase deficiencyU Wendel, E Wilichowski, J Schmidtke, et al.
Helvetica Paediatrica Acta|June 1, 1989
[Carbamyl phosphate synthase deficiency: clinical symptoms, diagnosis and dietary-medicamentous treatment in the neonatal period and infancy]H Hochreutener, J Issakainen, C Bachmann, et al.
Pageof 24