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J Arenas

Showing results (111-120 of 378) with videos related to

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Pediatric Neurology|July 1, 1995
Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndromeY Campos, T Garcia-Silva, C R Barrionuevo, et al.
FEBS Letters|March 14, 1994
Effects of L-carnitine on the pyruvate dehydrogenase complex and carnitine palmitoyl transferase activities in muscle of endurance athletesJ Arenas, R Huertas, Y Campos, et al.
Annals of Internal Medicine|November 1, 1987
Cyclosporine-induced acute renal failure in the nephrotic syndromeM Praga, R Martinez, M Lizasoain, et al.
Journal of the American Board of Family Medicine : JABFM|September 18, 2021
Associations of Race, Insurance, and Zip Code-Level Income with Nonadherence Diagnoses in Primary and Specialty Diabetes CareSourik Beltrán, Daniel J Arenas, Itzel J López-Hinojosa, et al.
Human Mutation|November 26, 1999
A novel missense mutation 15747 T>C in the mitochondrial cytochrome b geneI Aguilera, J R García-Lozano, J Bautista, et al.
Radiologia|October 4, 2007
[Holoprosencephaly. Role of magnetic resonance imaging in prenatal diagnosis]J Arenas Ramírez, P García González, B Duplá Paruges, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Clinical Chemistry|December 1, 1988
Activities of creatine kinase and its isoenzymes in serum in various skeletal muscle disordersJ Arenas, V Diaz, G Liras, et al.
American Journal of Human Genetics|October 16, 1999
About the "Pathological" role of the mtDNA T3308C mutationellipsisH Rocha, C Flores, Y Campos, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 8, 2000
Levels of nitric oxide are markedly increased in cerebrospinal fluid from patients with severe head injuryJ A Navarro-Gonzálvez, J Arenas, R Díez Lobato, et al.
Pageof 38

Showing results (111-120 of 378) with videos related to

Sort By:
Pageof 38
Pediatric Neurology|July 1, 1995
Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndromeY Campos, T Garcia-Silva, C R Barrionuevo, et al.
FEBS Letters|March 14, 1994
Effects of L-carnitine on the pyruvate dehydrogenase complex and carnitine palmitoyl transferase activities in muscle of endurance athletesJ Arenas, R Huertas, Y Campos, et al.
Annals of Internal Medicine|November 1, 1987
Cyclosporine-induced acute renal failure in the nephrotic syndromeM Praga, R Martinez, M Lizasoain, et al.
Journal of the American Board of Family Medicine : JABFM|September 18, 2021
Associations of Race, Insurance, and Zip Code-Level Income with Nonadherence Diagnoses in Primary and Specialty Diabetes CareSourik Beltrán, Daniel J Arenas, Itzel J López-Hinojosa, et al.
Human Mutation|November 26, 1999
A novel missense mutation 15747 T>C in the mitochondrial cytochrome b geneI Aguilera, J R García-Lozano, J Bautista, et al.
Radiologia|October 4, 2007
[Holoprosencephaly. Role of magnetic resonance imaging in prenatal diagnosis]J Arenas Ramírez, P García González, B Duplá Paruges, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A homozygous missense mutation (A659D) in the myophosphorylase gene in a Spanish patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Clinical Chemistry|December 1, 1988
Activities of creatine kinase and its isoenzymes in serum in various skeletal muscle disordersJ Arenas, V Diaz, G Liras, et al.
American Journal of Human Genetics|October 16, 1999
About the "Pathological" role of the mtDNA T3308C mutationellipsisH Rocha, C Flores, Y Campos, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 8, 2000
Levels of nitric oxide are markedly increased in cerebrospinal fluid from patients with severe head injuryJ A Navarro-Gonzálvez, J Arenas, R Díez Lobato, et al.
Pageof 38