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Molecular Genetics & Genomic Medicine|October 1, 2019
Mutational spectrum of Mexican patients with tyrosinemia type 1: In silico modeling and predicted pathogenic effect of a novel missense FAH variantIsabel Ibarra-González, Cynthia Fernández-Lainez, Miguel Angel Alcántara-Ortigoza, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|December 21, 2012
Liver exhibits thermal variations according to the stage of fibrosis progression: A novel use of modulated-differential scanning calorimetry for research in hepatologyGalileo Escobedo, José Luis Arjona-Román, Rosalía Meléndez-Pérez, et al.
Meta Gene|January 22, 2015
Polymorphism analysis and new JAG1 gene mutations of Alagille syndrome in Mexican populationEdgar Ricardo Vázquez-Martínez, Gustavo Varela-Fascinetto, Constanza García-Delgado, et al.
Plos One|April 28, 2010
Cellular senescence in livers from children with end stage liver diseaseGabriela Gutierrez-Reyes, Maria del Carmen Garcia de Leon, Gustavo Varela-Fascinetto, et al.
Annals of Hepatology|June 19, 2019
Guidelines for the diagnosis and treatment of extrahepatic portal vein obstruction (EHPVO) in childrenJudith Flores-Calderón, Segundo Morán-Villota, Solange-Heller Rouassant, et al.
Transplantation|May 21, 2016
Consensus, Dilemmas, and Challenges in Living Donor Liver Transplantation in Latin AmericaPaolo R Salvalaggio, João Seda Neto, Jefferson Andre Alves, et al.
International Journal of Molecular Sciences|August 14, 2025
A Retrospective Study of Clinical and Genetic Features in a Long-Term Cohort of Mexican Children with Alagille SyndromeRodrigo Vázquez-Frias, Gustavo Varela-Fascinetto, Carlos Patricio Acosta-Rodríguez-Bueno, et al.
The Journal of Allergy and Clinical Immunology. in Practice|January 28, 2023
Is Your Kid Actin Out? A Series of Six Patients With Inherited Actin-Related Protein 2/3 Complex Subunit 1B Deficiency and Review of the LiteratureEstefanía Vásquez-Echeverri, Marco Antonio Yamazaki-Nakashimada, Edna Venegas Montoya, et al.
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