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Fecha de publicación	Título	Autor(es)
2005	Descripción del cuadro clínico y defecto molecular de pacientes con enfermedad granulomatosa crónica en el Instituto Nacional de Pediatría	Staines Boone, Aide Tamara
2011	DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice	Randall Katrina L
2015	A novel CD40LG deletion causes the hyper-IgM syndrome with normal CD40L expression in a 6-month-old child	Lopez Herrera, Gabriela
2012	Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity	Lopez Herrera, Gabriela
2012	Increased pro-inflammatory cytokine production after lipopolysaccharide stimulation in patients with X-linked agammaglobulinemia	Gonzalez Serrano, Maria Edith
2016	Functional and Biochemical Characterization of Three Recombinant Human Glucose-6-Phosphate Dehydrogenase Mutants: Zacatecas, Vanua-Lava and Viangchan	Gómez Manzo, Saúl
2013	Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome	Nakamura K
2004	Sepsis grave por chromobacterium violaceum asociada a enfermedad granulomatosa crónica : reporte de un caso y revisión de la literatura	Cordova Ortega, Joaquin Antonio
2016	An uncommon inheritance pattern in Niemann-Pick disease type C: Identification of probable paternal germline mosaicism in a Mexican family	Cervera Gaviria M.,
2008	Analysis of the CTNS gene in nephropathic cystinosis Mexican patients: Report of four novel mutations and identification of a false positive 57-kb deletion genotype with LDM-2/exon 4 multiplex PCR assay	Alcántara Ortigoza, Miguel Ángel