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Resultados 31-40 de 71.
Resultados por ítem:
Fecha de publicaciónTítuloAutor(es)
2016A comparison of different antibiotic regimens for the treatment of infective endocarditisMartí Carvajal, Arturo J
2006Association analysis of the PTPN22 gene in childhood-onset systemic lupus erythematosus in Mexican populationBaca V.
2015Association of HMOX1 and NQO1 polymorphisms with metabolic syndrome componentsMartínez Hernández A
2015Clinical and Genotypic Spectrum of Chronic Granulomatous Disease in 71 Latin American Patients: First Report from the LASID RegistryBorges de Oliveira-Junior, Edgar
2013Características clínicas y terapéuticas de pacientes con inmunodeficiencia común variable en dos hospitales de tercer nivel de atención de la Ciudad de MéxicoDorbeker Azcona, Raúl
2013Clinical and genetic analysis of patients with X-linked hyper-IgM syndromeVargas Hernadez A
2008BCR-ABL, ETV6-RUNX1 and E2A-PBX1: Prevalence of the most common acute lymphoblastic leukemia fusion genes in Mexican patientsJimínez Morales S.,
2000Bart syndrome: The congenital localized absence of skin may follow the lines of Blaschko. Report of six casesDuran McKinster C.,
2013A multi-country study of intussusception in children under 2 years of age in Latin America: Analysis of prospective surveillance dataSáez Llorens, Xavier
2015A critical proton MR spectroscopy marker of Alzheimer's disease early neurodegenerative change: Low hippocampal NAA/Cr ratio impacts APOE ε 4 Mexico City children and their parentsCalderón Garcidueñas, Lilian