M. A. Ramírez-García

The intellectual developmental disorders Mexico study: situational diagnosis, burden, genomics and intervention proposal.

M. Medina-Mora, L. Salvador-Carulla, G. Ángeles, 2016, Salud publica de Mexico.

A Novel De Novo EFNB1 Gene Mutation in a Mexican Patient with Craniofrontonasal Syndrome

J. Zenteno, M. A. Ramírez-García, O. Chacon-Camacho, 2013, Case reports in genetics.

Brief Report: Delayed Diagnosis of Treatable Inborn Errors of Metabolism in Children with Autism and Other Neurodevelopmental Disorders

E. Lazcano-Ponce, I. Ibarra-González, M. Vela-Amieva, 2020, Journal of autism and developmental disorders.

Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice

Robert P. Carson, Robert C. Pedersen, Sean T. Hwang, 2022, JAMA neurology.

Clinical and Molecular Findings of Intermediate Allele Carriers in the HTT Gene from the Mexican Mestizo Population

S. Romero-Hidalgo, J. Zenteno, M. A. Ramírez-García, 2022, Neurodegenerative Diseases.

Strategies for decreasing the O2 content in the upgraded biogas purified via microalgae-based technology.

A. González-Sánchez, M. A. Ramírez-García, M. Franco-Morgado, 2020, Journal of environmental management.

Low quality of life, increased number of anti-seizure drugs, and the lack of caregiver support are associated with internalized stigma in adult Mexican patients with epilepsy

A. Fresán-Orellana, A. Jara-Prado, I. Martínez-Juárez, 2023, Epilepsy & Behavior.

Presymptomatic Testing for Huntington's Disease in Mexico: 28 Years of Experience.

M. A. Ramírez-García, M. Chávez-Oliveros, P. Yescas-Gómez, 2024, Archives of medical research.

Association of variants in the ABCB1, CYP2C19 and CYP2C9 genes for Juvenile Myoclonic Epilepsy.

A. Delgado-Escueta, A. Jara-Prado, R. Durón, 2023, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology.