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M Duran

Showing results (511-520 of 646) with videos related to

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Clinical Genetics|September 30, 2011
Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosisR Huijgen, A D M Stork, J C Defesche, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.
American Journal of Medical Genetics. Part A|January 15, 2005
Guanidinoacetate methyltransferase deficiency identified in adults and a child with mental retardationH Caldeira Araújo, W Smit, N M Verhoeven, et al.
Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology|November 11, 2019
Heart rate variability in the tegu lizard, Salvator merianae, its neuroanatomical basis and role in the assessment of recovery from experimental manipulationLivia M Duran, Edwin W Taylor, Pollyana V W Sanches, et al.
Analytical Biochemistry|February 22, 2001
Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolitesM F Silva, J P Ruiter, L IJlst, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 2, 1978
Nepsilon-(beta-Aspartyl)lysinuria in children with various pathological conditionsJ P Kamerling, G Aarsen, P K de Bree, et al.
Applied Optics|May 22, 2007
Phase tracking with a spatial synchronous methodJesús Muñoz-Maciel, Francisco G Peña-Lecona, Cesar Castillo-Quevedo, et al.
Journal of Inherited Metabolic Disease|August 13, 1998
Diagnosis and management of glutaric aciduria type II Barić, J Zschocke, E Christensen, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research|December 3, 2010
Acetoclastic methanogens in an anaerobic digester could be susceptible to trace metal supplementationC Park, A Bega, C Unlu, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresisJ A Smeitink, F A Beemer, M Espeel, et al.
Pageof 65

Showing results (511-520 of 646) with videos related to

Sort By:
Pageof 65
Clinical Genetics|September 30, 2011
Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosisR Huijgen, A D M Stork, J C Defesche, et al.
Neuromuscular Disorders : NMD|July 23, 1998
Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.
American Journal of Medical Genetics. Part A|January 15, 2005
Guanidinoacetate methyltransferase deficiency identified in adults and a child with mental retardationH Caldeira Araújo, W Smit, N M Verhoeven, et al.
Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology|November 11, 2019
Heart rate variability in the tegu lizard, Salvator merianae, its neuroanatomical basis and role in the assessment of recovery from experimental manipulationLivia M Duran, Edwin W Taylor, Pollyana V W Sanches, et al.
Analytical Biochemistry|February 22, 2001
Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolitesM F Silva, J P Ruiter, L IJlst, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 2, 1978
Nepsilon-(beta-Aspartyl)lysinuria in children with various pathological conditionsJ P Kamerling, G Aarsen, P K de Bree, et al.
Applied Optics|May 22, 2007
Phase tracking with a spatial synchronous methodJesús Muñoz-Maciel, Francisco G Peña-Lecona, Cesar Castillo-Quevedo, et al.
Journal of Inherited Metabolic Disease|August 13, 1998
Diagnosis and management of glutaric aciduria type II Barić, J Zschocke, E Christensen, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research|December 3, 2010
Acetoclastic methanogens in an anaerobic digester could be susceptible to trace metal supplementationC Park, A Bega, C Unlu, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresisJ A Smeitink, F A Beemer, M Espeel, et al.
Pageof 65