| Rights | Preview | Issue Date | Title | Author(s) | Type |
| openAccess |  | 2010 | Antithrombin Murcia (K241E) causing antithrombin deficiency: a possible role for altered glycosylation | Martínez-Martínez, Irene; Ordóñez, Adriana; Navarro-Fernández, José; Pérez-Lara, Ángel; Gutiérrez-Gallego, Ricardo; Giraldo, R.  ; Martínez, Constantino; Llop, Esther; Vicente, Vicente; Corral, Javier | Artículo |
| openAccess |  | 2018 | Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders | Bastida, J. M.; Lozano, Maria Luisa; Benito, Rocío; Janusz, Kamila; Palma-Barqueros, Verónica; Rey, Mónica del; Hernandez-Sánchez, Jesus M.; Riesco, Susana; Bermejo, Nuria; González-García, Hermenegildo; Rodriguez-Alén, Agustín; Aguilar, Carlos; Sevivas, Teresa; López-Fernández, María F.; Marneth, Anna E.; Reijden, Bert A. van der; Morgan, Neil V.; Watson, Steve P.; Vicente, Vicente; Hernández, Jesús M. ; Rivera, Jose; González-Porras, José R. | Artículo |
| openAccess |  | 2010 | L718P mutation in the membrane-proximal cytoplasmic tail of [beta]3 promotes abnormal [alpha]IIb[beta]3 clustering and lipid microdomain coalescence, and associates to thrombasthenia-like phenotype | Jayo, Asier ; Conde, Isabel ; Lastres, Pedro ; Martínez, Constantino; Rivera, José; Vicente, Vicente; González-Manchón, Consuelo | Artículo |
| closedAccess |  | Apr-2002 | Nonsense mutation in exon-19 of GPIIb associated with thrombasthenic phenotype. Failure of GPIIb(delta597-1008) to form stable complexes with GPIIIa | García Arias-Salgado, Elena ; Tao, Jianming; González-Manchón, Consuelo ; Butta, Nora ; Vicente, Vicente; Sánchez Ayuso, Matilde ; Parrilla, Roberto L. | Artículo |
| closedAccess |  | 2016 | Uniparental disomy causes deficiencies of vitamin K-dependent proteins | Dasi, M. A.; Gonzalez-Conejero, R.; Izquierdo, S.; Padilla, Jose; García, Juan L. ; Garcia-Barberá, N.; Argilés, B.; Morena-Barrio, M. E. de la; Hernandez-Sánchez, Jesus M.; Hernández, Jesús M. ; Vicente, Vicente; Corral, J. | Artículo |
| closedAccess |  | 2017 | Wiskott–Aldrich syndrome in a child presenting with macrothrombocytopenia | Bastida, J. M.; Rey, Mónica del; Revilla, Nuria; Benito, Rocío; Pérez-Andrés, Martin; González, Berta; Riesco, Susana; Janusz, Kamila; Padilla, Jose; Hortal Benito-Sendin, Ana; Bueno, David; Blanco, Elena; Hernández, Jesús M. ; Vicente, Vicente; Rivera, Jose; González-Porras, José R.; Lozano, Maria Luisa | Artículo |
