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M Pineda

Showing results (271-280 of 395) with videos related to

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Revista De Neurologia|October 10, 2002
[Angelman syndrome: physical characteristics and behavioural phenotype in 37 patients with confirmed genetic diagnosis]M Galván-Manso, J Campistol, E Monros, et al.
Leukemia|April 25, 2008
VTD combination therapy with bortezomib-thalidomide-dexamethasone is highly effective in advanced and refractory multiple myelomaM Pineda-Roman, M Zangari, F van Rhee, et al.
Biofactors (Oxford, England)|July 29, 2006
Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disordersR Montero, R Artuch, P Briones, et al.
Cureus|May 24, 2024
Bilateral Sixth Nerve Palsy: A Rare Presentation of Primary HypophysitisJosue D Pagoada-Torres, Rodolfo Villalobos-Díaz, Luz M Pineda-Centeno, et al.
The Journal of Invasive Cardiology|July 2, 2019
Trends and Outcomes of Alternative-Access Transcatheter Aortic Valve ReplacementAndrés M Pineda, Jennifer Rymer, Alice Wang, et al.
Cerebellum (London, England)|October 21, 2011
Mild clinical and biochemical phenotype in two patients with PMM2-CDG (congenital disorder of glycosylation Ia)M Casado, M M O'Callaghan, R Montero, et al.
The Journal of Heart Valve Disease|December 21, 2016
Bicuspid Aortic Valve and Aortic Root Morphology in Hispanic PatientsSofia A Horvath, Christos G Mihos, Juan P Rodriguez-Escudero, et al.
Neuropediatrics|December 7, 2007
Folate receptor autoantibodies and spinal fluid 5-methyltetrahydrofolate deficiency in Rett syndromeV T Ramaekers, J M Sequeira, R Artuch, et al.
Developmental Medicine and Child Neurology|September 21, 2007
Secondary abnormalities of neurotransmitters in infants with neurological disordersA García-Cazorla, M Serrano, B Pérez-Dueñas, et al.
Clinical Genetics|September 10, 2010
Molecular analysis of Sanfilippo syndrome type C in Spain: seven novel HGSNAT mutations and characterization of the mutant allelesI Canals, S C Elalaoui, M Pineda, et al.
Pageof 40

Showing results (271-280 of 395) with videos related to

Sort By:
Pageof 40
Revista De Neurologia|October 10, 2002
[Angelman syndrome: physical characteristics and behavioural phenotype in 37 patients with confirmed genetic diagnosis]M Galván-Manso, J Campistol, E Monros, et al.
Leukemia|April 25, 2008
VTD combination therapy with bortezomib-thalidomide-dexamethasone is highly effective in advanced and refractory multiple myelomaM Pineda-Roman, M Zangari, F van Rhee, et al.
Biofactors (Oxford, England)|July 29, 2006
Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disordersR Montero, R Artuch, P Briones, et al.
Cureus|May 24, 2024
Bilateral Sixth Nerve Palsy: A Rare Presentation of Primary HypophysitisJosue D Pagoada-Torres, Rodolfo Villalobos-Díaz, Luz M Pineda-Centeno, et al.
The Journal of Invasive Cardiology|July 2, 2019
Trends and Outcomes of Alternative-Access Transcatheter Aortic Valve ReplacementAndrés M Pineda, Jennifer Rymer, Alice Wang, et al.
Cerebellum (London, England)|October 21, 2011
Mild clinical and biochemical phenotype in two patients with PMM2-CDG (congenital disorder of glycosylation Ia)M Casado, M M O'Callaghan, R Montero, et al.
The Journal of Heart Valve Disease|December 21, 2016
Bicuspid Aortic Valve and Aortic Root Morphology in Hispanic PatientsSofia A Horvath, Christos G Mihos, Juan P Rodriguez-Escudero, et al.
Neuropediatrics|December 7, 2007
Folate receptor autoantibodies and spinal fluid 5-methyltetrahydrofolate deficiency in Rett syndromeV T Ramaekers, J M Sequeira, R Artuch, et al.
Developmental Medicine and Child Neurology|September 21, 2007
Secondary abnormalities of neurotransmitters in infants with neurological disordersA García-Cazorla, M Serrano, B Pérez-Dueñas, et al.
Clinical Genetics|September 10, 2010
Molecular analysis of Sanfilippo syndrome type C in Spain: seven novel HGSNAT mutations and characterization of the mutant allelesI Canals, S C Elalaoui, M Pineda, et al.
Pageof 40