Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maria Cristina Pascual Izquierdo"'
Autor:
Maria Cristina Pascual Izquierdo, Yolanda Martinez, Moraima Jiménez, Joan Cid, Aurora Viejo, Verónica Campuzano, Gemma Moreno Jiménez, David Valcárcel, Rosa Goterris, Miquel Lozano, Sandra Ortega, Ana Oliva, Luis Hernández, Sunil Lakhwani, Irene Garcia-Garcia, Jorge M. Nieto, Inmaculada Tallón, Saioa Zalba, Julio del Río-Garma, Miguel Fernández Zarzoso, Jon Ander Atucha Fernández, Maria Eva Mingot-Castellano, Inés Gómez-Seguí, Helena González, María Solé
Publikováno v:
Blood. 136:20-21
Introduction: Autoimmune thrombotic thrombocytopenic purpura (aTTP) is a severe disease caused by the production of autoantibodies against von Willebrand factor (vWF)-cleaving ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin-1 motifs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::110da1edcc85f442d91eec6e41bab904
https://doi.org/10.1182/blood-2020-136627
https://doi.org/10.1182/blood-2020-136627
Autor:
Isabel Caparrós, Gonzalo Caballero, Jose Angel Hernandez-Rivas, Miguel A. Sanz, Inmaculada Soto Ortega, Fernando Fernández-Fuertes, Luis Javier garcia Frade, Blanca Sanchez-Gonzalez, Isabel Regalado, Silvia Bernat, Pável E Olivera, Tomás José González-López, Isidro Jarque, Carmen Pastoriza, Maria Cristina Pascual Izquierdo, María Paz Martínez-Badas, Gloria Perez Segura, Daniel Martínez-Carballeira
Publikováno v:
Blood. 134:2352-2352
Background: Successful discontinuation of eltrombopag in certain immune thrombocytopenia (ITP) patients after complete response has already been demonstrated. However, the frequency of this phenomenon and type of candidate patients are still matter o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::273d084cb6ad094051e3df0fcb422344
https://doi.org/10.1182/blood-2019-129274
https://doi.org/10.1182/blood-2019-129274
Autor:
Angel Salgado, Cristina Amunarriz, M. Elena Moreno, Michael Calviño, Consuelo Martinez Redondo, Julio del Río-Garma, Margarita Berberana, Ana Oliva, Jose Garcia-Arroba, Gemma Mancebo Moreno, Rosa Goterris, Jesús Martín, Victoria Gonzalez, Jose Antonio Moreno, Faustino García-Candel, Luis Hernández, Julia Vidan, Jesus Fernandez-Sojo, Moreno M. Dolores, Carmen Fernandez, José Carlos Hernández, Aurora Viejo, Luisa Maria Guerra, Marina Gordillo, Joan Cid, Jose Maria Garcia-Gala, Nieves Alonso, M. Fernández, Melisa Daorta, Rafael Del Orbe, Maria Cristina Pascual Izquierdo, Sara Nistal Gil, Maite Calderon, Ramón Salinas, Javier de la Rubia, Maria Eva Mingot-Castellano, Sol Sanchez, Xavier Solanich, Esther Chica, Inés Gómez-Seguí, María Luisa Antelo, Carmen Ballester
Publikováno v:
Blood. 134:4910-4910
Introduction: Acquired thrombotic thrombocytopenic purpura (aTTP) is a rare disease characterized by a severe deficiency of the enzymatic activity of ADAMTS13 caused by autoantibodies, with an incidence of 3-4 x106inhabitants per year according to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8e053253dec6cae39e9ad5aa71b9f21
https://doi.org/10.1182/blood-2019-123258
https://doi.org/10.1182/blood-2019-123258