Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Débora Riverol"'
Autor:
Vicente Medina-Arana, Alberto Bravo, H. Díaz, Juan J. González-Aguilera, Antonia M. Fernández-Peralta, Eduardo Salido, L. González, Débora Riverol, Luciano Delgado
Publikováno v:
Familial Cancer. 10:265-271
Lynch syndrome (LS) is an autosomal dominant condition that predisposes to colorectal cancer and specific other tumors. Extracolonic tumors occur mainly in the endometrium, stomach, ovary, small intestine and urinary tract. The presence of rare tumor
Autor:
Patricia Ruiz-Garbajosa, Débora Riverol, María José Ramos, Antonio Sierra, Silvia Campos, Nínive Batista, Mar Ojeda-Vargas, Isabel Montesinos
Publikováno v:
Enfermedades Infecciosas y Microbiología Clínica. 28:430-434
Resumen Introduccion En julio de 2005 se aislo el primer Enterococcus faecium resistente a vancomicina (EFRV) genotipo vanA en el Hospital Universitario de Canarias en un paciente trasplantado renal ingresado en la Unidad de Nefrologia. En los meses
Autor:
Alejandro Jiménez, M.A. Miguel, Teresa Delgado, Antonio Sierra, Isabel Montesinos, Eduardo Salido, Débora Riverol
Publikováno v:
Journal of Hospital Infection. 64:257-263
This study investigated the molecular epidemiology of meticillin-resistant Staphylococcus aureus (MRSA) in the University Hospital of the Canary Islands (HUC) in order to evaluate epidemiological changes over a six-year period. Clinical and epidemiol
Autor:
Isabel, Montesinos, Silvia, Campos, María José, Ramos, Patricia, Ruiz-Garbajosa, Débora, Riverol, Nínive, Batista, Mar, Ojeda-Vargas, Antonio, Sierra
Publikováno v:
Enfermedades infecciosas y microbiologia clinica. 28(7)
In July, 2005 the first vancomycin-resistant Enterococcus faecium (VREF) with a genotype vanA was isolated in Hospital Universitario de Canarias (HUC). From September to December 2005, VREF vanA was isolated from another 15 patients (3 nosocomial inf
Publikováno v:
Investigacion clinica. 49(4)
Primary hyperoxaluria is a congenital innate error of the metabolism of the amino acids, that is transmitted like an autosomal recessive character. Two types of hyperoxaluria exist: the primary type I, that corresponds to the peroxisomal enzymatic de
Autor:
Noel Mesa-Torres, Israel Fabelo-Rosa, Debora Riverol, Cristina Yunta, Armando Albert, Eduardo Salido, Angel L Pey
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e71963 (2013)
Primary hyperoxaluria type I (PH1) is a conformational disease which result in the loss of alanine:glyoxylate aminotransferase (AGT) function. The study of AGT has important implications for protein folding and trafficking because PH1 mutants may cau
Externí odkaz:
https://doaj.org/article/c2378c142dc74d4a8ba7001559ea2f89