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 Jakobs

Showing results (71-80 of 417) with videos related to

Pageof 42
Sort By:
The Veterinary Record|February 18, 2005
L-2-hydroxyglutaric aciduria in a West Highland white terrierL S Garosi, J Penderis, J F McConnell, et al.
Journal of Neurology|May 16, 2009
A novel mutation as a cause of L-2-hydroxyglutaric aciduriaGed O'Connor, M King, G Salomons, et al.
European Journal of Clinical Nutrition|September 24, 2009
Patterns of free amino acids in German convenience food products: marked mismatch between label information and compositionM Hermanussen, U Gonder, C Jakobs, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|February 10, 2015
Endovascular aneurysm repair of aortoiliac aneurysms with an iliac side-branched stent graft: studying the morphological applicability of the Cook deviceD Gray, R Shahverdyan, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
The segregation of glutaryl-CoA dehydrogenase deficiency and Refsum syndrome in a familyE Christensen, N J Brandt, T Rosenberg, et al.
Biochimica Et Biophysica Acta|March 4, 1992
Identification of pristanoyl-CoA oxidase as a distinct, clofibrate non-inducible enzyme in rat liver peroxisomesR J Wanders, S Denis, C Jakobs, et al.
Progress in Clinical and Biological Research|January 1, 1992
Activation and oxidation of pristanic acid in rat liver: identification of a distinct, clofibrate non-inducible pristanoyl-CoA oxidaseR J Wanders, S Denis, C Jakobs, et al.
European Journal of Pediatrics|June 1, 1992
Further evaluation of Vigabatrin therapy in 4-hydroxybutyric aciduriaC Jakobs, T Michael, E Jaeger, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Retrospective diagnosis of carbohydrate-deficient glycoprotein syndrome type IbD M Neele, C M Kneepkens, N M Verhoeven, et al.
IUBMB Life|October 6, 2005
Murine succinate semialdehyde dehydrogenase (SSADH) deficiency, a heritable disorder of GABA metabolism with epileptic phenotypeK M Gibson, C Jakobs, P L Pearl, et al.
Pageof 42

Showing results (71-80 of 417) with videos related to

Sort By:
Pageof 42
The Veterinary Record|February 18, 2005
L-2-hydroxyglutaric aciduria in a West Highland white terrierL S Garosi, J Penderis, J F McConnell, et al.
Journal of Neurology|May 16, 2009
A novel mutation as a cause of L-2-hydroxyglutaric aciduriaGed O'Connor, M King, G Salomons, et al.
European Journal of Clinical Nutrition|September 24, 2009
Patterns of free amino acids in German convenience food products: marked mismatch between label information and compositionM Hermanussen, U Gonder, C Jakobs, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|February 10, 2015
Endovascular aneurysm repair of aortoiliac aneurysms with an iliac side-branched stent graft: studying the morphological applicability of the Cook deviceD Gray, R Shahverdyan, C Jakobs, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
The segregation of glutaryl-CoA dehydrogenase deficiency and Refsum syndrome in a familyE Christensen, N J Brandt, T Rosenberg, et al.
Biochimica Et Biophysica Acta|March 4, 1992
Identification of pristanoyl-CoA oxidase as a distinct, clofibrate non-inducible enzyme in rat liver peroxisomesR J Wanders, S Denis, C Jakobs, et al.
Progress in Clinical and Biological Research|January 1, 1992
Activation and oxidation of pristanic acid in rat liver: identification of a distinct, clofibrate non-inducible pristanoyl-CoA oxidaseR J Wanders, S Denis, C Jakobs, et al.
European Journal of Pediatrics|June 1, 1992
Further evaluation of Vigabatrin therapy in 4-hydroxybutyric aciduriaC Jakobs, T Michael, E Jaeger, et al.
Journal of Inherited Metabolic Disease|December 22, 1999
Retrospective diagnosis of carbohydrate-deficient glycoprotein syndrome type IbD M Neele, C M Kneepkens, N M Verhoeven, et al.
IUBMB Life|October 6, 2005
Murine succinate semialdehyde dehydrogenase (SSADH) deficiency, a heritable disorder of GABA metabolism with epileptic phenotypeK M Gibson, C Jakobs, P L Pearl, et al.
Pageof 42