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J Arenas

Showing results (281-290 of 378) with videos related to

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Radiologia|April 20, 2024
Prevalence and prognostic meaning of interstitial lung abnormalities in remote CT scans of patients with interstitial lung disease treated with antifibrotic therapyM M García Mullor, J J Arenas-Jiménez, A Ureña Vacas, et al.
Muscle & Nerve|March 1, 2002
Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathyY Campos, A García, A López, et al.
Journal of Inherited Metabolic Disease|March 30, 2018
Non-osteogenic muscle hypertrophy in children with McArdle diseaseI Rodríguez-Gómez, A Santalla, J Díez-Bermejo, et al.
Journal of the Neurological Sciences|September 10, 1997
Decreased cerebrospinal fluid levels of neutral and basic amino acids in patients with Parkinson's diseaseJ A Molina, F J Jiménez-Jiménez, P Gomez, et al.
Journal of the Neurological Sciences|September 15, 1996
Neurotransmitter amino acids in cerebrospinal fluid of patients with Parkinson's diseaseF J Jiménez-Jiménez, J A Molina, C Vargas, et al.
Transplantation Proceedings|November 22, 2005
Benefits of early biopsy on the outcome of kidney transplantationJ Dominguez, A Kompatzki, R Norambuena, et al.
International Journal of Sports Medicine|June 13, 2006
Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?M Pérez, M A Martin, S Cañete, et al.
Revista De Neurologia|January 19, 2000
[Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases]M Castro-Gago, V González-Conde, M J Fernández-Seara, et al.
Journal of Experimental & Clinical Cancer Research : CR|December 22, 1999
Matrix metalloproteinases expressed in squamous cell carcinoma of the oral cavity: correlation with clinicopathologic features and neo-adjuvant chemotherapy responseF J Arenas-Huertero, R Herrera-Goepfert, R Delgado-Chavez, et al.
Neuromuscular Disorders : NMD|June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathyY Campos, J Gámez, A García, et al.
Pageof 38

Showing results (281-290 of 378) with videos related to

Sort By:
Pageof 38
Radiologia|April 20, 2024
Prevalence and prognostic meaning of interstitial lung abnormalities in remote CT scans of patients with interstitial lung disease treated with antifibrotic therapyM M García Mullor, J J Arenas-Jiménez, A Ureña Vacas, et al.
Muscle & Nerve|March 1, 2002
Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathyY Campos, A García, A López, et al.
Journal of Inherited Metabolic Disease|March 30, 2018
Non-osteogenic muscle hypertrophy in children with McArdle diseaseI Rodríguez-Gómez, A Santalla, J Díez-Bermejo, et al.
Journal of the Neurological Sciences|September 10, 1997
Decreased cerebrospinal fluid levels of neutral and basic amino acids in patients with Parkinson's diseaseJ A Molina, F J Jiménez-Jiménez, P Gomez, et al.
Journal of the Neurological Sciences|September 15, 1996
Neurotransmitter amino acids in cerebrospinal fluid of patients with Parkinson's diseaseF J Jiménez-Jiménez, J A Molina, C Vargas, et al.
Transplantation Proceedings|November 22, 2005
Benefits of early biopsy on the outcome of kidney transplantationJ Dominguez, A Kompatzki, R Norambuena, et al.
International Journal of Sports Medicine|June 13, 2006
Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?M Pérez, M A Martin, S Cañete, et al.
Revista De Neurologia|January 19, 2000
[Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases]M Castro-Gago, V González-Conde, M J Fernández-Seara, et al.
Journal of Experimental & Clinical Cancer Research : CR|December 22, 1999
Matrix metalloproteinases expressed in squamous cell carcinoma of the oral cavity: correlation with clinicopathologic features and neo-adjuvant chemotherapy responseF J Arenas-Huertero, R Herrera-Goepfert, R Delgado-Chavez, et al.
Neuromuscular Disorders : NMD|June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathyY Campos, J Gámez, A García, et al.
Pageof 38