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Published in Molecular genetics & genomic medicine (01.11.2020)
Published in Molecular genetics & genomic medicine (01.11.2020)
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Carbajal Rodríguez, Luis, Navarrete Martínez, Juana Inés
Published in Acta pediátrica de México (2015)
Published in Acta pediátrica de México (2015)
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Newborn screening for six lysosomal storage disorders in a cohort of Mexican patients: Three-year findings from a screening program in a closed Mexican health system
Navarrete-Martínez, Juana Inés, Limón-Rojas, Ana Elena, Gaytán-García, Maria de Jesús, Reyna-Figueroa, Jesús, Wakida-Kusunoki, Guillermo, Delgado-Calvillo, Ma. del Rocío, Cantú-Reyna, Consuelo, Cruz-Camino, Héctor, Cervantes-Barragán, David Eduardo
Published in Molecular genetics and metabolism (01.05.2017)
Published in Molecular genetics and metabolism (01.05.2017)
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Are there biosimilar orphan drugs for Gaucher disease? An overview in Mexico
Castañeda-Hernández, G, Carbajal-Rodríguez, L, Cerón-Rodríguez, M, Correa- González, LC, Esquivel-Aguilar, A, Franco-Ornelas, SJ, García Ortiz, JE, Hernández- Guadarrama, CM, Navarrete-Martínez, JI, Santillán-Hernández, Y, Terreros-Muñoz, E
Published in GaBI Journal (01.06.2019)
Published in GaBI Journal (01.06.2019)
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Prevalencia de anemias hemolíticas hereditarias detectadas por tamiz metabólico ampliado en los servicios de salud de Petróleos Mexicanos
Hernández-Verdugo, Lizbeth Yamilet, Fernández-Bautista, María Fernanda, Domínguez-Camacho, Alejandra, Medina-Pérez, Cristal, Navarrete-Martínez, Juana Inés, Cervantes-Barragán, David Eduardo, Galindo-Delgado, Patricia
Published in Revista mexicana de pediatría (Sociedad Mexicana de Pediatría) (01.03.2023)
Published in Revista mexicana de pediatría (Sociedad Mexicana de Pediatría) (01.03.2023)
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