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Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
February 18, 2003
[Frequency of apolipoprotein E in a Nahua population]
Roberto Alfonso Suástegui Román, Petra Yescas Gómez, Jorge Luis Guerrero Camacho, et al.
Breast Cancer Research and Treatment
|
September 16, 2016
Clinical implications of routine genomic mutation sequencing in PIK3CA/AKT1 and KRAS/NRAS/BRAF in metastatic breast cancer
Juan Miguel Cejalvo, J Alejandro Pérez-Fidalgo, Gloria Ribas, et al.
Journal of Neuroscience Methods
|
September 11, 2020
Identification of brain structures and blood vessels by conventional ultrasound in rats
Mari Carmen Gómez-de Frutos, Iván García-Suárez, Fernando Laso-García, et al.
Digital Health
|
May 17, 2023
Neurodata Tracker: Software for computational assessment of hand motor skills based on optical motion capture in a virtual environment
David López, Laura Casado-Fernández, Fernando Fernández, et al.
Epilepsy & Behavior : E&B
|
June 15, 2016
High-dose versus low-dose valproate for the treatment of juvenile myoclonic epilepsy: Going from low to high
Laura E Hernández-Vanegas, Aurelio Jara-Prado, Adriana Ochoa, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
May 9, 2019
Letter to the Editor
Nancy Monroy-Jaramillo, Aurelio Cerón, Elizabeth León, et al.
Scientific Reports
|
March 31, 2019
The miRNA-449 family mediates doxorubicin resistance in triple-negative breast cancer by regulating cell cycle factors
Eduardo Tormo, Sandra Ballester, Anna Adam-Artigues, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
May 3, 2018
Phenotypic Variability in a Mexican Mestizo Family with Retinal Vasculopathy with Cerebral Leukodystrophy and TREX1 Mutation p.V235Gfs*6
Nancy Monroy-Jaramillo, Aurelio Cerón, Elizabeth León, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 13, 2007
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population
Elisa Alonso, Leticia Martínez-Ruano, Irene De Biase, et al.
Epilepsy Research
|
September 24, 2014
Late onset Lafora disease and novel EPM2A mutations: breaking paradigms
Aurelio Jara-Prado, Adriana Ochoa, María Elisa Alonso, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 106) with videos related to
Sort By:
Page
of 11
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
February 18, 2003
[Frequency of apolipoprotein E in a Nahua population]
Roberto Alfonso Suástegui Román, Petra Yescas Gómez, Jorge Luis Guerrero Camacho, et al.
Breast Cancer Research and Treatment
|
September 16, 2016
Clinical implications of routine genomic mutation sequencing in PIK3CA/AKT1 and KRAS/NRAS/BRAF in metastatic breast cancer
Juan Miguel Cejalvo, J Alejandro Pérez-Fidalgo, Gloria Ribas, et al.
Journal of Neuroscience Methods
|
September 11, 2020
Identification of brain structures and blood vessels by conventional ultrasound in rats
Mari Carmen Gómez-de Frutos, Iván García-Suárez, Fernando Laso-García, et al.
Digital Health
|
May 17, 2023
Neurodata Tracker: Software for computational assessment of hand motor skills based on optical motion capture in a virtual environment
David López, Laura Casado-Fernández, Fernando Fernández, et al.
Epilepsy & Behavior : E&B
|
June 15, 2016
High-dose versus low-dose valproate for the treatment of juvenile myoclonic epilepsy: Going from low to high
Laura E Hernández-Vanegas, Aurelio Jara-Prado, Adriana Ochoa, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
May 9, 2019
Letter to the Editor
Nancy Monroy-Jaramillo, Aurelio Cerón, Elizabeth León, et al.
Scientific Reports
|
March 31, 2019
The miRNA-449 family mediates doxorubicin resistance in triple-negative breast cancer by regulating cell cycle factors
Eduardo Tormo, Sandra Ballester, Anna Adam-Artigues, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion
|
May 3, 2018
Phenotypic Variability in a Mexican Mestizo Family with Retinal Vasculopathy with Cerebral Leukodystrophy and TREX1 Mutation p.V235Gfs*6
Nancy Monroy-Jaramillo, Aurelio Cerón, Elizabeth León, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 13, 2007
Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population
Elisa Alonso, Leticia Martínez-Ruano, Irene De Biase, et al.
Epilepsy Research
|
September 24, 2014
Late onset Lafora disease and novel EPM2A mutations: breaking paradigms
Aurelio Jara-Prado, Adriana Ochoa, María Elisa Alonso, et al.
Page
of 11