Acceder Registro /

ISABEL LOPEZ EXPOSITO

Buscador

Lozano-Rivas, N; Linares, LF; Marras-Fernandez-Cid, C; Garcia-Hernandez, AM; Alguero, MDC; Iniesta, F; Sanchez-Salinas, D; Lopez-Lucas, MD; Rodriguez-Valiente, M; Cabanas, V; Garcia-Bernal, D; Molina, MDM; Lopez, S; Ramirez-Tovar, F; Sara, JER; Garcia, B; Blanquer, M; Fernandez-Delgado, JAO; Espinosa, M; Zamarro, J; Becerra-Ratia, J; Peris, JL; Lopez-Exposito, I; Bafalliu, JA; Ruiz-Espejo, F; Domenech, E; Morales-Cano, MD; Arrabal, PM; Soler, G; Vera, A; Guzman-Aroca, F; Moraleda, JM; Sackstein, R. CLINICAL TRIAL OF INTRAVENOUS INFUSION OF FUCOSYLATED BONE MARROW MESENCHYMAL STEM CELLS IN PATIENTS WITH OSTEOPOROSIS. ANNALS OF THE RHEUMATIC DISEASES. 2018; 77:1625-1625. 10.1136/annrheumdis-2018-eular.4728
AÑO: 2018; IF: 14.299
Vera-Carbonell A, López-González V, Bafalliu JA, Ballesta-Martínez MJ, Fernández A, Guillén-Navarro E, López-Expósito I. Clinical comparison of 10q26 overlapping deletions: delineating the critical region for urogenital anomalies. Am J Med Genet A. 2015 Apr;167A(4):786-90. doi: 10.1002/ajmg.a.36949. PubMed PMID: 25655674.
AÑO: 2015; IF: 2.082
López-Expósito I, Ballesta-Martinez MJ, Bafalliu JA, Vera-Carbonell A, Domingo-Jiménez R, López-González V, Fernández A, Guillén-Navarro E. Array CGH detection of a novel cryptic deletion at 3q13 in a complex chromosome rearrangement. Genomics. 2014 Apr;103(4):288-91. doi: 10.1016/j.ygeno.2014.02.008. PubMed PMID: 24607569.
AÑO: 2014; IF: 2.284
Vera-Carbonell A, López-González V, Bafalliu JA, Piñero-Fernández J, Susmozas J, Sorli M, López-Pérez R, Fernández A, Guillén-Navarro E, López-Expósito I. Pre- and postnatal findings in a patient with a novel rec(8)dup(8q)inv(8)(p23.2q22.3) associated with San Luis Valley syndrome. Am J Med Genet A. 2013 Sep;161A(9):2369-75. doi: 10.1002/ajmg.a.36103. PubMed PMID: 23894102.
AÑO: 2013; IF: 2.048
Sánchez-Ferrer ML, Machado-Linde F, Martínez-Espejo Cerezo A, Peñalver Parres C, Ferri B, López-Expósito I, Abad L, Parrilla JJ. Management of a dichorionic twin pregnancy with a normal fetus and an androgenetic diploid complete hydatidiform mole. Fetal Diagn Ther. 2013;33(3):194-200. doi: 10.1159/000338926. PubMed PMID: 22832009.
AÑO: 2013; IF: 2.295

Instituto de Investigación Sanitaria Acreditado

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Fondo Social Europeo "El FSE Invierte en tu futuro"

Fondo Social Europeo

Sello de Calidad Europeo "HR Excellence in Research"

HRS4R