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 (501-510 of 646) with videos related to

Pageof 65
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1988
Beta-mannosidosis in two brothers with hearing lossL Dorland, M Duran, F E Hoefnagels, et al.
Environmental Management|March 6, 2018
Comparison of Recent Oil and Gas, Wind Energy, and Other Anthropogenic Landscape Alteration Factors in Texas Through 2014Jon Paul Pierre, Brad D Wolaver, Benjamin J Labay, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 22, 2008
[Short-chain acyl-CoA dehydrogenase deficiency (SCADD): relatively high prevalence in the Netherlands and strongly variable fenotype; neonatal screening not indicated]B T van Maldegem, M Duran, R J A Wanders, et al.
American Journal of Human Genetics|May 11, 2006
Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathyS Ferdinandusse, P Kostopoulos, S Denis, et al.
American Journal of Human Genetics|September 1, 1993
A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)B S Andresen, P Bross, T G Jensen, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.
The Journal of Pediatrics|September 1, 1985
Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acidsM Duran, G Mitchell, J B de Klerk, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|March 26, 2004
Fatty acids and homocysteine levels in patients with recurrent depression: an explorative pilot studyJ Assies, A Lok, C L Bockting, et al.
The Journal of Cell Biology|June 27, 2020
Correction: The function of GORASPs in Golgi apparatus organization in vivoRianne Grond, Tineke Veenendaal, Juan M Duran, et al.
The Journal of Heart Valve Disease|March 4, 2000
Significant increase of aortic root volume and commissural area occurs prior to aortic valve openingD C Pang, S J Choo, H H Luo, et al.
Pageof 65

Showing results (501-510 of 646) with videos related to

Sort By:
Pageof 65
Journal of Inherited Metabolic Disease|January 1, 1988
Beta-mannosidosis in two brothers with hearing lossL Dorland, M Duran, F E Hoefnagels, et al.
Environmental Management|March 6, 2018
Comparison of Recent Oil and Gas, Wind Energy, and Other Anthropogenic Landscape Alteration Factors in Texas Through 2014Jon Paul Pierre, Brad D Wolaver, Benjamin J Labay, et al.
Nederlands Tijdschrift Voor Geneeskunde|August 22, 2008
[Short-chain acyl-CoA dehydrogenase deficiency (SCADD): relatively high prevalence in the Netherlands and strongly variable fenotype; neonatal screening not indicated]B T van Maldegem, M Duran, R J A Wanders, et al.
American Journal of Human Genetics|May 11, 2006
Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathyS Ferdinandusse, P Kostopoulos, S Denis, et al.
American Journal of Human Genetics|September 1, 1993
A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)B S Andresen, P Bross, T G Jensen, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.
The Journal of Pediatrics|September 1, 1985
Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acidsM Duran, G Mitchell, J B de Klerk, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|March 26, 2004
Fatty acids and homocysteine levels in patients with recurrent depression: an explorative pilot studyJ Assies, A Lok, C L Bockting, et al.
The Journal of Cell Biology|June 27, 2020
Correction: The function of GORASPs in Golgi apparatus organization in vivoRianne Grond, Tineke Veenendaal, Juan M Duran, et al.
The Journal of Heart Valve Disease|March 4, 2000
Significant increase of aortic root volume and commissural area occurs prior to aortic valve openingD C Pang, S J Choo, H H Luo, et al.
Pageof 65