47,XXY/48,XXXY/49,XXXXY mosaic with hydrocephaly: a case report and review of the literature

by Dueñas-Arias Jesús E, Aguilar-Medina Maribel, Arámbula-Meraz Eliakym, Valenzuela-Camacho Juliana B, Vega-Solano Angelina, Granados Julio, Ramos-Payán Rosalío
Published 2007-09-01

Kernicterus by glucose-6-phosphate dehydrogenase deficiency: a case report and review of the literature

by Cossio de Gurrola Gladys, Araúz Juan, Durán Elfilda, Aguilar-Medina Maribel, Ramos-Payán Rosalío, García-Magallanes Noemí, Pacheco Gerardo, Arámbula Meraz Eliakym
Published 2008-05-01

Tetralogy of Fallot associated with macrocephaly-capillary malformation syndrome: a case report and review of the literature

by Dueñas-Arias Jesus E, Arámbula-Meraz Eliakym, Frías-Castro Luis O, Ramos-Payán Rosalio, Quibrera-Matienzo Jose A, Luque-Ortega Fred, Aguilar-Medina E Maribel
Published 2009-09-01

Identification of novel mutation in cathepsin C gene causing Papillon-Lefèvre Syndrome in Mexican patients

by Romero-Quintana José G, Frías-Castro Luis O, Arámbula-Meraz Eliakym, Aguilar-Medina Maribel, Dueñas-Arias Jesús E, Melchor-Soto Jesús D, Romero-Navarro José G, Ramos-Payán Rosalío
Published 2013-01-01