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J Arenas

Showing results (241-250 of 378) with videos related to

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Neurologia (Barcelona, Spain)|October 1, 1994
[Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases]J Arpa, Y Campos, A Cruz Martínez, et al.
Human Mutation|June 22, 2000
Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiencyM A Martín, J C Rubio, P del Hoyo, et al.
Cancer Research|April 27, 2021
The Transcription Factor SLUG Uncouples Pancreatic Cancer Progression from the RAF-MEK1/2-ERK1/2 PathwayFaiz Bilal, Enrique J Arenas, Kim Pedersen, et al.
Journal of Child Neurology|March 12, 1999
Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunctionM Castro-Gago, A Alonso, E Pintos-Martínez, et al.
Muscle & Nerve|July 9, 1999
Molecular analysis in Spanish patients with muscle carnitine palmitoyltransferase deficiencyM A Martín, J C Rubio, F De Bustos, et al.
Anales De Medicina Interna (Madrid, Spain : 1984)|January 1, 1993
[Levels of lipoprotein(a), other lipids and lipoproteins in adolescents from the health area of Alcoy]J J Arenas Jiménez, C Quílez Ivorra, J F Sastre Pascual, et al.
Neurology|February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibersJ Arenas, Y Campos, B Bornstein, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIEA Blazquez, M A Martín, M C Lara, et al.
Plants (Basel, Switzerland)|December 11, 2022
Susceptibility of Novel Promising Citrus Rootstocks to White Root RotJuan M Arjona-López, Frederick G Gmitter, Estefanía Romero-Rodríguez, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|July 1, 1992
An electrically powered total artificial heart. Over 1 year survival in the calfA J Snyder, G Rosenberg, J Reibson, et al.
Pageof 38

Showing results (241-250 of 378) with videos related to

Sort By:
Pageof 38
Neurologia (Barcelona, Spain)|October 1, 1994
[Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases]J Arpa, Y Campos, A Cruz Martínez, et al.
Human Mutation|June 22, 2000
Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiencyM A Martín, J C Rubio, P del Hoyo, et al.
Cancer Research|April 27, 2021
The Transcription Factor SLUG Uncouples Pancreatic Cancer Progression from the RAF-MEK1/2-ERK1/2 PathwayFaiz Bilal, Enrique J Arenas, Kim Pedersen, et al.
Journal of Child Neurology|March 12, 1999
Congenital hydranencephalic-hydrocephalic syndrome associated with mitochondrial dysfunctionM Castro-Gago, A Alonso, E Pintos-Martínez, et al.
Muscle & Nerve|July 9, 1999
Molecular analysis in Spanish patients with muscle carnitine palmitoyltransferase deficiencyM A Martín, J C Rubio, F De Bustos, et al.
Anales De Medicina Interna (Madrid, Spain : 1984)|January 1, 1993
[Levels of lipoprotein(a), other lipids and lipoproteins in adolescents from the health area of Alcoy]J J Arenas Jiménez, C Quílez Ivorra, J F Sastre Pascual, et al.
Neurology|February 5, 1999
A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibersJ Arenas, Y Campos, B Bornstein, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIEA Blazquez, M A Martín, M C Lara, et al.
Plants (Basel, Switzerland)|December 11, 2022
Susceptibility of Novel Promising Citrus Rootstocks to White Root RotJuan M Arjona-López, Frederick G Gmitter, Estefanía Romero-Rodríguez, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|July 1, 1992
An electrically powered total artificial heart. Over 1 year survival in the calfA J Snyder, G Rosenberg, J Reibson, et al.
Pageof 38