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A Cabello

Showing results (111-120 of 239) with videos related to

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Physical Review Letters|August 8, 2009
Experimental test of quantum contextuality in neutron interferometryH Bartosik, J Klepp, C Schmitzer, et al.
Brain : a Journal of Neurology|October 1, 1986
Hereditary motor and sensory neuropathy type II. Clinicopathological study of a familyJ Berciano, O Combarros, J Figols, et al.
The British Journal of Oral & Maxillofacial Surgery|November 24, 2024
Arthroscopic anatomy of the anteromedial wall of the temporomandibular joint: Implications in articular disc displacementB García-Medina, A Cabello-Serrano, A Martínez-Sahuquillo, et al.
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.
Neurocirugia (Asturias, Spain)|March 28, 2006
Complete surgical resection of high-grade astroblastoma with long time survival: case report and review of the literatureP Miranda, R D Lobato, A Cabello, et al.
Diabetes|January 1, 1986
Chlorpropamide raises fructose-2,6-bisphosphate concentration and inhibits gluconeogenesis in isolated rat hepatocytesL Monge, M Mojena, J L Ortega, et al.
Journal of the Neurological Sciences|March 8, 2000
Time window for clinical effectiveness of mass evacuation in a rat balloon model mimicking an intraparenchymatous hematomaE Lopez Valdes, A Hernandez Lain, L Calandre, et al.
Revista Espanola De Cardiologia|June 1, 1994
[Multiple heart valve involvement in renal polycystic disease in the adult]F López Pardo, A Cabello González, I Moreno Maqueda, et al.
Acta Neuropathologica|June 27, 2000
Suprasellar chordoid gliomaJ R Ricoy, R D Lobato, B Báez, 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.
Pageof 24

Showing results (111-120 of 239) with videos related to

Sort By:
Pageof 24
Physical Review Letters|August 8, 2009
Experimental test of quantum contextuality in neutron interferometryH Bartosik, J Klepp, C Schmitzer, et al.
Brain : a Journal of Neurology|October 1, 1986
Hereditary motor and sensory neuropathy type II. Clinicopathological study of a familyJ Berciano, O Combarros, J Figols, et al.
The British Journal of Oral & Maxillofacial Surgery|November 24, 2024
Arthroscopic anatomy of the anteromedial wall of the temporomandibular joint: Implications in articular disc displacementB García-Medina, A Cabello-Serrano, A Martínez-Sahuquillo, et al.
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.
Neurocirugia (Asturias, Spain)|March 28, 2006
Complete surgical resection of high-grade astroblastoma with long time survival: case report and review of the literatureP Miranda, R D Lobato, A Cabello, et al.
Diabetes|January 1, 1986
Chlorpropamide raises fructose-2,6-bisphosphate concentration and inhibits gluconeogenesis in isolated rat hepatocytesL Monge, M Mojena, J L Ortega, et al.
Journal of the Neurological Sciences|March 8, 2000
Time window for clinical effectiveness of mass evacuation in a rat balloon model mimicking an intraparenchymatous hematomaE Lopez Valdes, A Hernandez Lain, L Calandre, et al.
Revista Espanola De Cardiologia|June 1, 1994
[Multiple heart valve involvement in renal polycystic disease in the adult]F López Pardo, A Cabello González, I Moreno Maqueda, et al.
Acta Neuropathologica|June 27, 2000
Suprasellar chordoid gliomaJ R Ricoy, R D Lobato, B Báez, 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.
Pageof 24