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

M Duran

Showing results (491-500 of 646) with videos related to

Pageof 65
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1996
Mitochondrial very long-chain acyl-CoA dehydrogenase deficiency with a mild clinical courseB Merinero, C Pérez-Cerdá, M J Garcia, et al.
Journal of Inherited Metabolic Disease|July 13, 2004
Glutathione synthetase deficiency associated with antenatal cerebral bleedingL W Brüggemann, F Groenendaal, E Ristoff, et al.
American Journal of Translational Research|May 22, 2012
Validation of transcatheter left ventricular electromechanical mapping for assessment of cardiac function and targeted transendocardial injection in a porcine ischemia-reperfusion modelSharven Taghavi, Jason M Duran, Remus M Berretta, et al.
American Heart Journal|March 30, 2002
Coronary stent implantation in patients older than 75 years of age: clinical profile and initial and long-term (3 years) outcomeJuan C Muñoz, Joaquín J Alonso, Juan M Duran, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Abnormal glutathione conjugation in patients with tyrosinaemia type IT M Mulders, D J Bergman, B T Poll-The, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation?B Assmann, G F Hoffmann, L Wagner, et al.
The Journal of Cell Biology|June 24, 2020
The function of GORASPs in Golgi apparatus organization in vivoRianne Grond, Tineke Veenendaal, Juan M Duran, et al.
Pediatric Research|February 1, 1987
A new case of purine nucleoside phosphorylase deficiency: enzymologic, clinical, and immunologic characteristicsG Rijksen, W Kuis, S K Wadman, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Identification of two novel mutations C79X and R235Q in the dihydropyrimidine dehydrogenase gene in a patient presenting with hematuriaA B P van Kuilenburg, J Meijer, D Dobritzsch, et al.
Plos One|September 14, 2019
Upgraded molecular models of the human KCNQ1 potassium channelGeorg Kuenze, Amanda M Duran, Hope Woods, et al.
Pageof 65

Showing results (491-500 of 646) with videos related to

Sort By:
Pageof 65
Journal of Inherited Metabolic Disease|January 1, 1996
Mitochondrial very long-chain acyl-CoA dehydrogenase deficiency with a mild clinical courseB Merinero, C Pérez-Cerdá, M J Garcia, et al.
Journal of Inherited Metabolic Disease|July 13, 2004
Glutathione synthetase deficiency associated with antenatal cerebral bleedingL W Brüggemann, F Groenendaal, E Ristoff, et al.
American Journal of Translational Research|May 22, 2012
Validation of transcatheter left ventricular electromechanical mapping for assessment of cardiac function and targeted transendocardial injection in a porcine ischemia-reperfusion modelSharven Taghavi, Jason M Duran, Remus M Berretta, et al.
American Heart Journal|March 30, 2002
Coronary stent implantation in patients older than 75 years of age: clinical profile and initial and long-term (3 years) outcomeJuan C Muñoz, Joaquín J Alonso, Juan M Duran, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
Abnormal glutathione conjugation in patients with tyrosinaemia type IT M Mulders, D J Bergman, B T Poll-The, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation?B Assmann, G F Hoffmann, L Wagner, et al.
The Journal of Cell Biology|June 24, 2020
The function of GORASPs in Golgi apparatus organization in vivoRianne Grond, Tineke Veenendaal, Juan M Duran, et al.
Pediatric Research|February 1, 1987
A new case of purine nucleoside phosphorylase deficiency: enzymologic, clinical, and immunologic characteristicsG Rijksen, W Kuis, S K Wadman, et al.
Nucleosides, Nucleotides & Nucleic Acids|July 5, 2008
Identification of two novel mutations C79X and R235Q in the dihydropyrimidine dehydrogenase gene in a patient presenting with hematuriaA B P van Kuilenburg, J Meijer, D Dobritzsch, et al.
Plos One|September 14, 2019
Upgraded molecular models of the human KCNQ1 potassium channelGeorg Kuenze, Amanda M Duran, Hope Woods, et al.
Pageof 65