| Non-invasive biomarkers for Duchenne muscular dystrophy and carrier detection MA Anaya-Segura, FA García-Martínez, LÁ Montes-Almanza, BG Díaz, ... Molecules 20 (6), 11154-11172, 2015 | 53 | 2015 |
| Immunodetection analysis of muscular dystrophies in Mexico B Gómez‐Díaz, H Rosas‐Vargas, B Roque‐Ramírez, P Meza‐Espinoza, ... Muscle & nerve 45 (3), 338-345, 2012 | 43 | 2012 |
| Distrofia muscular de Duchenne: actualidad y perspectivas de tratamiento LB López-Hernández, NA Vázquez-Cárdenas, E Luna-Padrón Rev Neurol 49 (7), 369-75, 2009 | 36 | 2009 |
| Distrofias musculares en México: un enfoque clínico, bioquímico y molecular RMC Vázquez, LBL Hernández, LÁR Calderón, BG Díaz, FF Valverde, ... Revista de Especialidades Médico-Quirúrgicas 15 (3), 152-160, 2010 | 24 | 2010 |
| Duplication of SOX9 associated with 46, XX ovotesticular disorder of sex development B López-Hernández, JP Méndez, RM Coral-Vázquez, ... Reproductive BioMedicine Online 37 (1), 107-112, 2018 | 23 | 2018 |
| Comparison of mutation profiles in the Duchenne muscular dystrophy gene among populations: implications for potential molecular therapies LB López-Hernández, B Gómez-Díaz, AB Luna-Angulo, M Anaya-Segura, ... International journal of molecular sciences 16 (3), 5334-5346, 2015 | 22 | 2015 |
| Duchenne muscular dystrophy in a developing country: challenges in management and genetic counseling LB López-Hernández, B Gomez-Diaz, RE Escobar-Cedillo, ... Genetic counseling 25 (2), 129, 2014 | 20 | 2014 |
| Genetic structure and forensic parameters of 38 Indels for human identification purposes in eight Mexican populations G Martínez-Cortés, L Gusmão, R Pereira, VH Salcido, ... Forensic Science International: Genetics 17, 149-152, 2015 | 18 | 2015 |
| Low prevalence of most frequent pathogenic variants of six PARK genes in sporadic Parkinson’s disease S García, L López-Hernández, JA Suarez-Cuenca, M Solano-Rojas, ... Folia neuropathologica 52 (1), 22-29, 2014 | 17 | 2014 |
| Peripheral blood transcriptome profiling enables monitoring disease progression in dystrophic mice and patients M Signorelli, M Ebrahimpoor, O Veth, K Hettne, N Verwey, ... EMBO Molecular Medicine 13 (4), e13328, 2021 | 16 | 2021 |
| Serum levels of microRNA-206 and novel mini-STR assays for carrier detection in Duchenne muscular dystrophy MA Anaya-Segura, H Rangel-Villalobos, G Martínez-Cortés, ... International Journal of Molecular Sciences 17 (8), 1334, 2016 | 16 | 2016 |
| Analysis of ERCC1 and ERCC2 gene variants in osteosarcoma, colorectal and breast cancer B Gómez-Díaz, M de la Luz Ayala-Madrigal, M Gutiérrez-Angulo, ... Oncology Letters 9 (4), 1657-1661, 2015 | 15 | 2015 |
| Quality and safety in healthcare for medical students: challenges and the road ahead LB López-Hernández, BG Díaz, EO Zamora González, ... Healthcare 8 (4), 540, 2020 | 13 | 2020 |
| Low proteolytic clipping of histone H3 in cervical cancer J Sandoval-Basilio, N Serafín-Higuera, OD Reyes-Hernandez, ... Journal of Cancer 7 (13), 1856, 2016 | 13 | 2016 |
| Functional polymorphism rs13306560 of the MTHFR gene is associated with essential hypertension in a Mexican-Mestizo population JC Pérez-Razo, LJ Cano-Martínez, G Vargas Alarcón, ... Circulation: Cardiovascular Genetics 8 (4), 603-609, 2015 | 13 | 2015 |
| Mecanismos de señalización intracelular en cáncer de tiroides P Mondragón-Terán, LB López-Hernández, J Gutiérrez-Salinas, ... Cirugía y Cirujanos 84 (5), 434-443, 2016 | 12 | 2016 |
| Association of the rs1801133 variant in the MTHFR gene and sporadic Parkinson’s disease S García, RM Coral-Vázquez, MP Gallegos-Arreola, LÁ Montes-Almanza, ... Folia neuropathologica 53 (1), 24-28, 2015 | 12 | 2015 |
| Permeabilidad intestinal y eje intestino–hígado E Gómez-Cortés, RPC de Vaca, JE Martínez-Hernández, ... Revista de Especialidades Médico-Quirúrgicas 20 (1), 83-89, 2015 | 11 | 2015 |
| Diagnóstico y tratamiento con esteroides de pacientes con distrofia muscular de Duchenne: experiencia y recomendaciones para México NA Vázquez-Cárdenas, F Ibarra-Hernández, LB López-Hernández, ... Rev Neurol 57, 455-62, 2013 | 11 | 2013 |
| Genotype-phenotype discordance in a Duchenne muscular dystrophy patient due to a novel mutation: insights into the shock absorber function of dystrophin LB López-Hernández, D van Heusden, MA Soriano-Ursúa, ... Revista de Neurologia 52 (12), 720-724, 2011 | 9 | 2011 |
Ramón Mauricio Coral VázquezProfesor Escuela Superior de Medicina IPN在 ipn.mx 的电子邮件经过验证
