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Resultados por ítem:

Fecha de publicación	Título	Autor(es)
2015	Association of HMOX1 and NQO1 polymorphisms with metabolic syndrome components	Martínez Hernández A
2015	Clinical and Genotypic Spectrum of Chronic Granulomatous Disease in 71 Latin American Patients: First Report from the LASID Registry	Borges de Oliveira-Junior, Edgar
2013	Características clínicas y terapéuticas de pacientes con inmunodeficiencia común variable en dos hospitales de tercer nivel de atención de la Ciudad de México	Dorbeker Azcona, Raúl
2013	Clinical and genetic analysis of patients with X-linked hyper-IgM syndrome	Vargas Hernadez A
2008	BCR-ABL, ETV6-RUNX1 and E2A-PBX1: Prevalence of the most common acute lymphoblastic leukemia fusion genes in Mexican patients	Jimínez Morales S.,
2000	Benign cephalic histiocytosis progressing into juvenile xanthogranuloma: A non-Langerhans cell histiocytosis transforming under the influence of a virus?	Rodriguez Jurado R.,
2013	A multi-country study of intussusception in children under 2 years of age in Latin America: Analysis of prospective surveillance data	Sáez Llorens, Xavier
2015	Cysticidal activity of extracts and isolated compounds from Teloxys graveolens: In vitro and in vivo studies	Palomares Alonso Francisca
2015	A critical proton MR spectroscopy marker of Alzheimer's disease early neurodegenerative change: Low hippocampal NAA/Cr ratio impacts APOE Îµ 4 Mexico City children and their parents	Calderón Garcidueñas, Lilian
2014	Persistencia bilateral de la arteria hialoidea. Reporte de un caso	Borbolla Pertierra A.M.,