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J Arenas

Showing results (91-100 of 378) with videos related to

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Boletin Medico Del Hospital Infantil De Mexico|February 9, 2018
[Microtia-atresia: clinical, genetic and genomic aspects]Mónica Aguinaga-Ríos, Sara Frías, Diego J Arenas-Aranda, et al.
Revista Clinica Espanola|March 8, 2018
Reply to «Visibility of healthcare research institutes through the Web of Science database»R Barredo Torices, M López Berlanga, I de Mier Barragán, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Variable clinical expression associated with the mutation 3243 np of mitochondrial DNAY Campos, J Bautista, E Gutierrez-Rivas, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNAY Campos, M A Martín, J Vaamonde, et al.
American Journal of Clinical Pathology|August 20, 2023
Virtual biopsies: Proof of concept for a novel quantitative approach to liver biopsy adequacy and pathology educationJacob R Sweeney, Daniel J Arenas, Danielle Fortuna, et al.
Metabolism: Clinical and Experimental|January 24, 1998
The association of acetyl-L-carnitine with glucose and lipid metabolism in human muscle in vivo: the effect of hyperinsulinemiaP Ebeling, J A Tuominen, J Arenas, et al.
Neuroradiology|January 20, 2000
Mitochondrial diseases in children: neuroradiological and clinical features in 17 patientsA Muñoz, F Mateos, R Simón, et al.
Mycopathologia|April 29, 1977
[Epidemic outbreak of tinea corporis due to Microsporum gypseum]B Sierra de Arroyave, A Yepes, J Arenas, et al.
Muscle & Nerve|December 11, 1999
A missense mutation W797R in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.
Human Mutation|February 19, 2000
Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Pageof 38

Showing results (91-100 of 378) with videos related to

Sort By:
Pageof 38
Boletin Medico Del Hospital Infantil De Mexico|February 9, 2018
[Microtia-atresia: clinical, genetic and genomic aspects]Mónica Aguinaga-Ríos, Sara Frías, Diego J Arenas-Aranda, et al.
Revista Clinica Espanola|March 8, 2018
Reply to «Visibility of healthcare research institutes through the Web of Science database»R Barredo Torices, M López Berlanga, I de Mier Barragán, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Variable clinical expression associated with the mutation 3243 np of mitochondrial DNAY Campos, J Bautista, E Gutierrez-Rivas, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNAY Campos, M A Martín, J Vaamonde, et al.
American Journal of Clinical Pathology|August 20, 2023
Virtual biopsies: Proof of concept for a novel quantitative approach to liver biopsy adequacy and pathology educationJacob R Sweeney, Daniel J Arenas, Danielle Fortuna, et al.
Metabolism: Clinical and Experimental|January 24, 1998
The association of acetyl-L-carnitine with glucose and lipid metabolism in human muscle in vivo: the effect of hyperinsulinemiaP Ebeling, J A Tuominen, J Arenas, et al.
Neuroradiology|January 20, 2000
Mitochondrial diseases in children: neuroradiological and clinical features in 17 patientsA Muñoz, F Mateos, R Simón, et al.
Mycopathologia|April 29, 1977
[Epidemic outbreak of tinea corporis due to Microsporum gypseum]B Sierra de Arroyave, A Yepes, J Arenas, et al.
Muscle & Nerve|December 11, 1999
A missense mutation W797R in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.
Human Mutation|February 19, 2000
Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Pageof 38