Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Cristina Pascual-Izquierdo"'
Autor:
Maria del Mar Meijon-Ortigueira, Isabel Solares, Cecilia Muñoz-Delgado, Sinziana Stanescu, Marta Morado, Cristina Pascual-Izquierdo, Lucía Villalon Blanco, Amaya Belanger Quintana, Covadonga Pérez Menéndez-Conde, Montserrat Morales-Conejo, Jesús Villarrubia-Espinosa
Publikováno v:
Biomedicines, Vol 12, Iss 3, p 579 (2024)
Gaucher disease is an inherited disorder in which there is a deficiency of the enzyme glucocerebrosidase, which leads to the accumulation of glucosylceramide. Although much scientific evidence is now available, there is still limited data on the impa
Externí odkaz:
https://doaj.org/article/c0b14991a0d948f48d6d5020a2c89ed5
Autor:
Tomás José González-López, Abelardo Bárez, Angel Bernardo-Gutiérrez, Silvia Bernat, Mariana Canaro-Hirnyk, Laura Entrena-Ureña, Fernando Fernández-Fuertes, José María Guinea de Castro, Reyes Jiménez-Bárcenas, Cristina Pascual-Izquierdo, Blanca Sánchez-González, Isidro Jarque
Publikováno v:
Infectious Diseases and Therapy, Vol 12, Iss 2, Pp 303-315 (2022)
Abstract Primary immune thrombocytopenia (ITP) is an acquired autoimmune disease with highly variable presentation, characteristics, and clinical course. Thrombocytopenia is a common complication of many viral infections, including SARS-CoV-2. In add
Externí odkaz:
https://doaj.org/article/9d60d1cdd8804819acff85433f980a34
Autor:
Marie Scully, Jovanna Baptista, Indranil Bhattacharya, Spero Cataland, Paul Coppo, Loredana Cuccia, Tina Dutt, Shih-Han Susan Huang, Cristina Pascual Izquierdo, María Eva Mingot-Castellano, Aric Parnes, Katerina Pavenski, Kavitha Rajavel, Isidro Jarque, Linda T. Wang, Miguel Fernández Zarzoso, Andy Zhu, Björn Mellgård
Publikováno v:
HemaSphere, Vol 7, p e8651306 (2023)
Externí odkaz:
https://doaj.org/article/9d54802998ac49a9a2cc851f16a18103
Autor:
Inés Gómez Seguí, Eva Frances Aracil, Mingot-Castellano Maria Eva, M Vara Pampliega, Rosa Goterris, F García Candel, Cristina Pascual Izquierdo, Julio del Rio Garma, Luisa Guerra Dominguez, Isabel Vicuña Andrés, Jose Garcia-Arroba Peinado, Saioa Zalba Marcos, Julia Vidan Estevez, Elena Gonzalez, Veronica Campuzano Saavedra, Jose Maria Garcia Gala, S Ortega Sanchez, Jorge Martínez Nieto, Laura Pardo Gambarte, Maria Sole Rodríguez, Marta Fernandez Docampo, Laura F. Ávila Idrovo, Luis M. Hernández, Joan Cid, Javier DE LA Rubia
Publikováno v:
HemaSphere, Vol 7, p e929835e (2023)
Externí odkaz:
https://doaj.org/article/3045e0557cd34ae480e28590145bc2b0
Autor:
Javier DE LA Rubia, Inés Gómez-Seguí, Joan Cid, David Valcárcel, Rosa Goterris, Miguel Fernández Zarzoso, María Eva Mingot-Castellano, Cristina Pascual Izquierdo, Ana Oliva Hernández, Jorge Martínez Nieto, Laura F. Ávila Idrovo, María Liz Paciello Coronel, Luis M. Hernández
Publikováno v:
HemaSphere, Vol 7, p e61163bd (2023)
Externí odkaz:
https://doaj.org/article/9045b3c1f2ff47c4bfd77ac66e872a16
Autor:
Mariana Bastos‐Oreiro, Javier Ortiz, Virginia Pradillo, Eduardo Salas, Carolina Marínez‐Laperche, Andrés Muñoz, Ismael Buño, José Luis Diéz‐Martin, Jose Manuel Soria, Cristina Pascual Izquierdo
Publikováno v:
Cancer Medicine, Vol 10, Iss 21, Pp 7585-7592 (2021)
Abstract Background The incorporation of genetic variables into risk scores for predicting venous thromboembolic events (VTE) could improve their capacity to identify those patients for whom thromboprophylaxis would be most beneficial. Proof‐of‐c
Externí odkaz:
https://doaj.org/article/021f82f706714db2a1f0bf6a63bba45f
Autor:
Fernando García-Boyano, Clara M. Castro Ávila, Miguel Arguello-Tomás, Álvaro Moreno Cuervo, José Manuel Ligero Ramos, Cristina Pascual-Izquierdo
Publikováno v:
Annals of Vascular Surgery - Brief Reports and Innovations, Vol 2, Iss 3, Pp 100102- (2022)
Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a syndrome that resembles to heparin-induced thrombocytopenia (HIT). Platelet factor 4 (PF-4) reacts to a vaccine component resulting formation of immune complex that stimulates an autoimmu
Externí odkaz:
https://doaj.org/article/3a2385cfa2cd4a3c92fcafa5c49761b3
Autor:
María Eva Mingot-Castellano, José María Bastida, Gonzalo Caballero-Navarro, Laura Entrena Ureña, Tomás José González-López, José Ramón González-Porras, Nora Butta, Mariana Canaro, Reyes Jiménez-Bárcenas, María del Carmen Gómez del Castillo Solano, Blanca Sánchez-González, Cristina Pascual-Izquierdo, on behalf of the GEPTI
Publikováno v:
Pharmaceuticals, Vol 15, Iss 7, p 779 (2022)
Primary immune thrombocytopenia (ITP) is an autoimmune disorder that causes low platelet counts and subsequent bleeding risk. Although current corticosteroid-based ITP therapies are able to improve platelet counts, up to 70% of subjects with an ITP d
Externí odkaz:
https://doaj.org/article/8391b7c27bbe4a9cbc81a84cc39a076f
Autor:
María Eva Mingot-Castellano, Nora Butta, Mariana Canaro, María del Carmen Gómez del Castillo Solano, Blanca Sánchez-González, Reyes Jiménez-Bárcenas, Cristina Pascual-Izquierdo, Gonzalo Caballero-Navarro, Laura Entrena Ureña, Tomás José González-López, on behalf of the GEPTI
Publikováno v:
Vaccines, Vol 10, Iss 6, p 961 (2022)
Worldwide vaccination against SARS-CoV-2 has allowed the detection of hematologic autoimmune complications. Adverse events (AEs) of this nature had been previously observed in association with other vaccines. The underlying mechanisms are not totally
Externí odkaz:
https://doaj.org/article/9a6016f6518641e89ea83f10372fba19
Autor:
Inés Gómez-Seguí, Cristina Pascual Izquierdo, María Eva Mingot Castellano, Javier de la Rubia Comos
Publikováno v:
Expert Review of Hematology. 16:17-32
Severe ADAMTS13 deficiency defines thrombotic thrombocytopenic purpura (TTP). ADAMTS13 is responsible for VWF cleavage. In the absence of this enzyme, widespread thrombi formation occurs, causing microangiopathic anemia and thrombocytopenia, and lead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9b126bda18654be7bc54038aaf5a021
https://doi.org/10.1080/17474086.2023.2159803
https://doi.org/10.1080/17474086.2023.2159803