Instituto Nacional de Pediatría: Buscar

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Resultados 51-60 de 101.

Resultados por ítem:

Fecha de publicación	Título	Autor(es)
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.,
2000	Bart syndrome: The congenital localized absence of skin may follow the lines of Blaschko. Report of six cases	Duran McKinster C.,
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.,
2009	Lactante de 1 mes y 20 días de edad con palidez generalizada y petequias diseminadas	Guillén Orozco M.R.
2012	CYP2W1, CYP4F11 and CYP8A1 polymorphisms and interaction of CYP2W1 genotypes with risk factors in mexican women with breast cancer	Cárdenas Rodríguez, Noemí