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V Delgado

Showing results (451-460 of 468) with videos related to

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American Journal of Human Genetics|June 3, 2008
Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsyMiyabi Tanaka, Richard W Olsen, Marco T Medina, et al.
Archivos De Cardiologia De Mexico|May 28, 2020
Evaluation of pharmacoinvasive strategy versus percutaneous coronary intervention in patients with acute myocardial infarction with ST segment elevation at the National Institute of Cardiology (PHASE-MX)Luis A Baeza-Herrera, Diego Araiza-Garaygordobil, Rodrigo Gopar-Nieto, et al.
Revista De Neurologia|June 12, 2023
[Family planning in men and women with multiple sclerosis. Analysis of the Andalusian Registry (2018-2022)]D Vidal-de Francisco, C Rosa-Garrido, M Ruiz-de Arcos, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|April 27, 2017
Current MitraClip experience, safety and feasibility in the NetherlandsZ Rahhab, F A Kortlandt, J F Velu, et al.
Advances in Neurology|October 29, 2004
Familial juvenile myoclonic epilepsyMaría Elisa Alonso, Marco T Medina, Iris E Martínez-Juárez, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2016
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causalityJulia N Bailey, Christopher Patterson, Laurence de Nijs, et al.
Neurology|May 30, 2008
Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsyM T Medina, T Suzuki, M E Alonso, et al.
Journal of Animal Breeding and Genetics = Zeitschrift Fur Tierzuchtung Und Zuchtungsbiologie|September 15, 2015
Genetic relationships among American donkey populations: insights into the process of colonizationJ Jordana, A Ferrando, J Miró, et al.
Nature Genetics|July 20, 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, et al.
Advances in Neurology|October 29, 2004
Childhood absence epilepsy evolving to juvenile myoclonic epilepsy: electroclinical and genetic featuresMarco T Medina, Reyna M Durón, María E Alonso, et al.
Pageof 47

Showing results (451-460 of 468) with videos related to

Sort By:
Pageof 47
American Journal of Human Genetics|June 3, 2008
Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsyMiyabi Tanaka, Richard W Olsen, Marco T Medina, et al.
Archivos De Cardiologia De Mexico|May 28, 2020
Evaluation of pharmacoinvasive strategy versus percutaneous coronary intervention in patients with acute myocardial infarction with ST segment elevation at the National Institute of Cardiology (PHASE-MX)Luis A Baeza-Herrera, Diego Araiza-Garaygordobil, Rodrigo Gopar-Nieto, et al.
Revista De Neurologia|June 12, 2023
[Family planning in men and women with multiple sclerosis. Analysis of the Andalusian Registry (2018-2022)]D Vidal-de Francisco, C Rosa-Garrido, M Ruiz-de Arcos, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|April 27, 2017
Current MitraClip experience, safety and feasibility in the NetherlandsZ Rahhab, F A Kortlandt, J F Velu, et al.
Advances in Neurology|October 29, 2004
Familial juvenile myoclonic epilepsyMaría Elisa Alonso, Marco T Medina, Iris E Martínez-Juárez, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 29, 2016
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causalityJulia N Bailey, Christopher Patterson, Laurence de Nijs, et al.
Neurology|May 30, 2008
Novel mutations in Myoclonin1/EFHC1 in sporadic and familial juvenile myoclonic epilepsyM T Medina, T Suzuki, M E Alonso, et al.
Journal of Animal Breeding and Genetics = Zeitschrift Fur Tierzuchtung Und Zuchtungsbiologie|September 15, 2015
Genetic relationships among American donkey populations: insights into the process of colonizationJ Jordana, A Ferrando, J Miró, et al.
Nature Genetics|July 20, 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, et al.
Advances in Neurology|October 29, 2004
Childhood absence epilepsy evolving to juvenile myoclonic epilepsy: electroclinical and genetic featuresMarco T Medina, Reyna M Durón, María E Alonso, et al.
Pageof 47