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Nuria Bermejo Vega
Nuria Bermejo Vega
Complejo Hospitalario Universitario de Cáceres. Hospital San Pedro de Alcántara
Geverifieerd e-mailadres voor ses.juntaextremadura.net
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Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)
P Knoebl, P Marco, F Baudo, P Collins, A Huth‐Kühne, L Nemes, ...
Journal of Thrombosis and Haemostasis 10 (4), 622-631, 2012
5642012
Management of bleeding in acquired hemophilia A: results from the European Acquired Haemophilia (EACH2) Registry
F Baudo, P Collins, A Huth-Kühne, H Lévesque, P Marco, L Nemes, ...
Blood, The Journal of the American Society of Hematology 120 (1), 39-46, 2012
4122012
Immunosuppression for acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)
P Collins, F Baudo, P Knoebl, H Lévesque, L Nemes, F Pellegrini, ...
Blood, The Journal of the American Society of Hematology 120 (1), 47-55, 2012
3722012
Pregnancy-associated acquired haemophilia A: results from the European Acquired Haemophilia (EACH2) registry.
CP Tengborn L, Baudo F, Huth-Kühne A, Knoebl P, E contributors.
BJOG: An International Journal of Obstetrics & Gynaecology 119 (12), 1529-37, 2012
1392012
Bleeding risk of surgery and its prevention in patients with inherited platelet disorders
S Orsini, P Noris, L Bury, PG Heller, C Santoro, RA Kadir, NC Butta, ...
haematologica 102 (7), 1192, 2017
1202017
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
JM Bastida, ML Lozano, R Benito, K Janusz, V Palma-Barqueros, ...
haematologica 103 (1), 148, 2018
1182018
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: a communication from the Platelet Physiology SSC
P Gresele, S Orsini, P Noris, E Falcinelli, MC Alessi, L Bury, M Borhany, ...
Journal of Thrombosis and Haemostasis 18 (3), 732-739, 2020
782020
Molecular and clinical profile of von Willebrand disease in Spain (PCM–EVW–ES): Proposal for a new diagnostic paradigm
J Batlle, A Pérez-Rodríguez, I Corrales, MF López-Fernández, ...
Thromb Haemost 115 (1), 40-50, 2016
692016
Relationship between calcium mobilization and platelet α-and δ-granule secretion. A role for TRPC6 in thrombin-evoked δ-granule exocytosis
E Lopez, N Bermejo, A Berna-Erro, N Alonso, GM Salido, PC Redondo, ...
Archives of biochemistry and biophysics 585, 75-81, 2015
572015
Design and application of a 23‐gene panel by next‐generation sequencing for inherited coagulation bleeding disorders
JM Bastida, M Del Rey, ML Lozano, ME Sarasquete, R Benito, ...
Haemophilia 22 (4), 590-597, 2016
552016
STIM1 tyrosine-phosphorylation is required for STIM1-Orai1 association in human platelets
E Lopez, I Jardin, A Berna-Erro, N Bermejo, GM Salido, SO Sage, ...
Cellular signalling 24 (6), 1315-1322, 2012
462012
Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes
JM Bastida, JR González-Porras, C Jiménez, R Benito, GR Ordoñez, ...
Thrombosis and haemostasis 26 (01), 66-74, 2017
442017
Homers regulate calcium entry and aggregation in human platelets: a role for Homers in the association between STIM1 and Orai1
J Isaac, A Letizia, B Nuria, MS Gines, AR Juan
Biochemical Journal 445 (1), 29-38, 2012
432012
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients
N Borràs, J Batlle, A Pérez-Rodríguez, MF López-Fernández, ...
Haematologica 102 (12), 2005, 2017
422017
Real-life management of primary immune thrombocytopenia (ITP) in adult patients and adherence to practice guidelines
ML Lozano, N Revilla, TJ Gonzalez-Lopez, S Novelli, JR González-Porras, ...
Annals of hematology 95 (7), 1089–1098, 2016
392016
Identification of seven novel SMPD1 mutations causing Niemann-Pick disease types A and B
PM Irun P, Mallén M, Dominguez C, Rodriguez-Sureda V
Clin Genet 84 (4), 356-361, 2013
352013
Efficacy, safety and pharmacokinetics of a new high‐purity factor X concentrate in subjects with hereditary factor X deficiency
SK Austin, K Kavakli, M Norton, F Peyvandi, A Shapiro
Haemophilia 22 (3), 419–425, 2016
312016
Filamin A Modulates Store-Operated Ca2+ Entry by Regulating STIM1 (Stromal Interaction Molecule 1)–Orai1 Association in Human Platelets
JJ Lopez, L Albarrán, I Jardín, J Sanchez-Collado, PC Redondo, ...
Arteriosclerosis, thrombosis, and vascular biology 38 (2), 386-397, 2018
292018
Long-term mTOR inhibitors administration evokes altered calcium homeostasis and platelet dysfunction in kidney transplant patients.
RPC López E, Berna-Erro A, Bermejo N, Brull JM
J Cell Mol Med, 2013
262013
Deciphering predictive factors for choice of thrombopoietin receptor agonist, treatment free responses, and thrombotic events in immune thrombocytopenia
ML Lozano, ME Mingot-Castellano, MM Perera, I Jarque, ...
Scientific Reports 9 (1), 16680, 2019
222019
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Artikelen 1–20