Tipo |
Título / Nombre |
Autor(es) |
Año |
|
Ten New Cases of Hermansky-Pudlak Syndrome in the Iberian Peninsula: Identification of Novel Genetic Variants in HPS3, HPS4, HPS6 and DTNBP1 Associated with Significant Clinical Complications |
Bastida JM, Morais S, Palma-Barqueros V, Benito R, Bermejo N, Karkucak M, Trapero-Marugan M, Bohdan N, Pereira M, Marín-Quílez A, Oliveira J, Yucel Y, Santos R, González-Porras JR, Lima M, Rivera J |
2018 |
|
Coagulación intravascular diseminada |
Bermejo Vega N |
2018 |
|
Diagnosis and management of von Willebrand disease in Spain |
Batlle J, Pérez-Rodríguez A, Corrales I, Borràs N, Rodríguez-Trillo Á, Lourés E, Cid AR, Bonanad S, Cabrera N, Moret A, Parra R, Mingot-Castellano ME, Navarro N, Altisent C, Pérez-Montes R, Marcellini S, Moreto A, Herrero S, Soto I, Fernández-Mosteirín N, Jiménez-Yuste V, Alonso N, de Andrés Jacob A, Fontánez E, Campos R, Paloma MJ, Bermejo Vega N, Berrueco R, Mateo J, Arribalzaga K, Marco P, Palomo Á, Castro Quismondo N, Iñigo B, Nieto MDM, Vidal R, Martínez MP, Aguinaco R, Tenorio M, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Dobom M, Aguilar C, Batlle López F, Vidal F, López-Fernández MF |
2018 |
|
Role of multimeric analysis of von Willebrand factor (VWF) in von Willebrand disease (VWD) diagnosis: Lessons from the PCM-EVW-ES Spanish project |
Pérez-Rodríguez A, Batlle J, Corrales I, Borràs N, Rodríguez-Trillo Á, Lourés E, Cid AR, Bonanad S, Cabrera N, Moret A, Parra R, Mingot-Castellano ME, Navarro N, Altisent C, Pérez-Montes R, Marcellini S, Moreto A, Herrero S, Soto I, Fernández Mosteirín N, Jiménez-Yuste V, Alonso N, de Andrés Jacob A, Fontanes E, Campos R, Paloma MJ, Bermejo N, Berrueco R, Mateo J, Arribalzaga K, Marco P, Palomo Á, Castro Quismondo N, Iñigo B, Nieto MDM, Vidal R, Martínez MP, Aguinaco R, Tenorio M, Ferreiro M, García-Frade J, Rodríguez-Huerta AM, Cuesta J, Rodríguez-González R, García-Candel F, Dobón M, Aguilar C, Batlle F, Vidal F, López-Fernández MF |
2018 |
|
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders |
Bastida JM, Lozano ML, Benito R, Janusz K, Palma-Barqueros V, Del Rey M, Hernández-Sánchez JM, Riesco S, Bermejo N, González-García H, Rodriguez-Alén A, Aguilar C, Sevivas T, López-Fernández MF, Marneth AE, van der Reijden BA, Morgan NV, Watson SP, Vicente V, Hernández-Rivas JM, Rivera J, González-Porras JR |
2018 |
|
Stanniocalcin 2 Regulates Non-capacitative Ca2+ Entry and Aggregation in Mouse Platelets |
López E, Gómez-Gordo L, Cantonero C, Bermejo N, Pérez-Gómez J, Granados MP, Salido GM, Rosado Dionisio JA, Redondo Liberal PC |
2018 |
|
Filamin A Modulates Store-Operated Ca2+ Entry by Regulating STIM1 (Stromal Interaction Molecule 1)-Orai1 Association in Human Platelets |
López JJ, Albarrán L, Jardín I, Sánchez-Collado J, Redondo PC, Bermejo N, Bobe R, Smani T, Rosado JA |
2018 |
|
Síndrome coronario agudo en pacientes con trombocitopenia. Respuesta |
Bermejo N |
2017 |
|
Long Term Antiaggregation in a Patient with Severe Factor XI Deficiency |
Sigüenza R, Bermejo N, Casas I, Pérez Leal F, Cáceres S, Ibáñez F |
2017 |
|
Effect of Pregnancy on the Clinical Course of ITP Pregnant Women and Their Newborns. Resuts of a Spanish Case Series of 297 Primary ITP Pregnancies |
González-López TJ, Olivera P, Jarque I, Bastida JM, Bernat S, Sánchez-González B, Bolaños E, Pérez-Rus G, Huerta AR, Fernández-Fuertes F, Martínez-Robles V, Martínez-Badas MP, Pérez-Montes R, Penarrubia Ponce MJ, Conesa V, Bermejo N, Caballero G, Álvarez Román MT, Fernández-Miñano C, Guerrero L, Marcellini S, Sierra Pacho M, Pardal E, Pastoriza C, López Ansoar ME, de Cabo E, Hermida G, Sanz MA |
2017 |