Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Álvarez Román, MT"'
Autor:
Alvarèz Román, MT, Benitez Hidalgo, O, Blatny, J, Bührlen, M, Carvalho, M, Castaman, G, Chambost, H, Rosa Cid, A, Escuriola-Ettingshausen, C, Fischer, K, Van Geet, C, Gretenkort Andersson, N, Kartal-Kaess, M, Knudsen, H, Königs, C, Koskenvuo, M, Male, C, Stamm Mikkelsen, T, Molinari, A, Motwani, J, Nolan, B, d’Oiron, R, Oldenburg, J, Olivieri, M, Oudot, C, Pergantou, H, Pinto, F, Ranta, S, Zápotocká, E, Kenet, G, Carcao, M, Rivard, G, Fischer, Kathelijn, Kenet, Gili, Kurnik, Karin, Carcao, Manuel, Oldenburg, Johannes, Stamm-Mikkelsen, Torben, Cid Haro, Ana Rosa, Koskenvuo, Minna, Blatny, Jan, Königs, Christoph
Publikováno v:
In Blood Advances 23 January 2024 8(2):369-377
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology and severity of the associated bleeding symptoms are highly heterogeneous, adding to the difficulties of diagnosis and management. Evidence-based guid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::a394a2e63c85181b88c838cff66e4c92
https://openaccess.sgul.ac.uk/id/eprint/113572/1/1-s2.0-S0268960X21000394-main.pdf
https://openaccess.sgul.ac.uk/id/eprint/113572/1/1-s2.0-S0268960X21000394-main.pdf
Autor:
Álvarez Román, MT, Butta Coll, N, García Barcenilla, S, Pérez González, L, de la Plaza Collazo, I, De la Corte Rodríguez, H, Romero Garrido, JA, Martín Salces, M, Rivas Pollmar, MI, Cebanu, T, González‐Zorrilla, E, Acuña, P, Monzón Manzano, E, Merchán, EC, Trelles Martínez, R, Blanco Bañares, MJ, Gutiérrez Alvariño, M, Jiménez Yuste, V
Publikováno v:
Haemophilia
Introduction We present the first registry of patients with congenital bleeding disorders and COVID‐19. The study has been carried out in the Community of Madrid, which has the highest number of cases in Spain. The objective is to understand the in
Autor:
Garcia-Martínez I, Borràs N, Martorell M, Parra R, Altisent C, Ramírez L, Álvarez-Román MT, Nuñez R, Megias-Vericat JE, Corrales I, Alonso S, Vidal F
Publikováno v:
THROMBOSIS AND HAEMOSTASIS
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
The pharmacokinetic (PK) response of severe hemophilia A (HA) patients to infused factor VIII (FVIII) shows substantial variability. Several environmental and genetic factors are associated with changes in FVIII plasma levels and infused FVIII PK. Ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::1bcab0f49cb0a4ebbf2225b3a2073aa5
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=13144
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=13144
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Fernandez-Bello, Ihosvany *, Alvarez-Román, MT *, de la Corte-Rodríguez, H *, Butta, N *, Hernández-Moreno, AL *, Rivas Muñoz, S *, Martín-Salces, M *, Rodriguez-Merchan, EC *, Canales Albendea, Miguel, Jiménez-Yuste, V *
Publikováno v:
In Blood 2 December 2016 128(22):4975-4975
Autor:
Jose María Guinea de Castro, M. Fernanda López-Fernández, Maria Luisa Lozano, M. Teresa Álvarez Román, Blanca Sánchez González, Tomás José González-López, Luis Fernando Fernández Fuertes, Isidro Jarque, David Valcárcel Ferreiras, Jose Ramon Gonzalez Porras, M. Eva Mingot-Castellano
Publikováno v:
Advances in Hematology, Vol 2019 (2019)
Advances in Hematology
Scientia
Advances in Hematology
Scientia
Delphi method; Primary immune thrombocytopenia; Clinical guideline Método Delphi; Trombocitopenia inmune primaria; Guía clínica Consens Delphi; Trombocitopènia immune primària; Guia clínica Background and Objective. Diagnosis and management of
Autor:
José Luis Trillo-Mata, Amparo Santamaría, José Luis Poveda, María Teresa Álvarez-Román, M. Tort, José Antonio Vinagre Romero, Ignacio Cuervo-Arango, Rafael Pérez-Santamarina, X. Badia
Publikováno v:
Scientia
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Recercat. Dipósit de la Recerca de Catalunya
instname
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Haemophilia A; Inhibitors; Drug value Hemofilia A; Inhibidores; Valores del medicamento Hemofília A; Inhibidors; Valors del medicament Patients with moderate to severe haemophilia A are at a higher risk of developing FVIII inhibitors that require th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f85a2e3f250c03a2157cb40f081c9eb1
http://hdl.handle.net/11351/5216
http://hdl.handle.net/11351/5216
Autor:
Álvarez Román MT; Thrombosis and Haemostasis Unit, University Hospital La Paz, Madrid, Spain., Kragh N; Sobi, Swedish Orphan Biovitrum AB, 112 76, Stockholm, Sweden. nana.kragh@sobi.com., Guyot P; Sanofi, Cambridge, MA, USA., Wilson A; Sanofi, Cambridge, MA, USA., Wojciechowski P; Assignity, Krakow, Poland.; Putnam PHMR, Krakow, Poland., Margas W; Assignity, Krakow, Poland.; Putnam PHMR, Krakow, Poland., Wdowiak M; Putnam PHMR, Krakow, Poland., Santagostino E; Sobi, Basel, Switzerland., Arnaud A; Sanofi, Cambridge, MA, USA.
Publikováno v:
Advances in therapy [Adv Ther] 2024 Nov 22. Date of Electronic Publication: 2024 Nov 22.
Autor:
Oldenburg J; Institute of Experimental Hematology and Transfusion Medicine, University Hospital Bonn, Medical Faculty, University of Bonn, Bonn, Germany., Hay C; University Department of Haematology, Manchester Royal Infirmary, Manchester, UK., Peyvandi F; Angelo Bianchi Bonomi Hemophilia and Thrombosis Center and Fondazione Luigi Villa, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy.; Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy., Tagliaferri A; Regional Reference Center for Inherited Bleeding Disorders, University Hospital of Parma, Parma, Italy., Holme PA; Department of Haematology, Oslo University Hospital, Institute of Clinical Medicine, University of Oslo, Oslo, Norway., Álvarez-Román MT; Department of Haematology, La Paz University Hospital-IdiPaz, Madrid, Spain., Biron-Andréani C; Haemophilia Treatment Centre, Department of Biological Haematology, University Hospital Montpellier, Montpellier, France., Malmström H; Observational Research, Sobi, Stockholm, Sweden., Bystrická L; Global Medical Affairs and Clinical Development, Sobi, Stockholm, Sweden., Lethagen S; Global Medical Affairs and Clinical Development, Sobi, Stockholm, Sweden.; Haemostasis and Thrombosis Centre, Copenhagen University, Copenhagen, Denmark.
Publikováno v:
European journal of haematology [Eur J Haematol] 2024 Oct 21. Date of Electronic Publication: 2024 Oct 21.