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Nuria Bermejo

Hospital Universitario La Paz
H指数:18
被引数:1,064

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Optimizing Surgical Approaches for Patients with Inherited Factor VII Deficiency

优化遗传性凝血因子Ⅶ缺乏症患者的手术方法

2026-01-010
PRE
Association of laboratory test results with the bleeding history in patients with inherited platelet function disorders (the Bleeding Assesment Tool- LABoratory tests substudy): communication from the Platelet Physiology ISTH-SSC
2024-01-011
OAAI
Multicenter evaluation of light transmission platelet aggregation reagents: communication from the ISTH SSC Subcommittee on Platelet Physiology
2023-09-016
OAAI
Deciphering predictive factors for choice of thrombopoietin receptor agonist, treatment free responses, and thrombotic events in immune thrombocytopenia (vol 11, 16867, 2021)
2021-08-131
OAAI
A novel genetic variant in PTGS1 affects N-glycosylation of cyclooxygenase-1 causing a dominant-negative effect on platelet function and bleeding diathesis
2021-01-054
OAAI
Unraveling the Influence of Common von Willebrand factor variants on von Willebrand Disease Phenotype: An Exploratory Study on the Molecular and Clinical Profile of von Willebrand Disease in Spain Cohort

von Willebrand因子常见变异对von Willebrand病表型的影响: 西班牙队列中von Willebrand病的分子和临床特征的探索性研究

2020-03-053
PREAI
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC

ISTH/SSC出血评估工具对遗传性血小板疾病的验证: 来自血小板生理学SSC的交流

2020-03-0176
OAAI
Deciphering predictive factors for choice of thrombopoietin receptor agonist, treatment free responses, and thrombotic events in immune thrombocytopenia
2019-11-1319
OAAI
Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing
2019-04-1615
OAAI
Joint status in Spanish haemophilia B patients assessed using the Haemophilia Early Arthropathy Detection with Ultrasound (HEAD-US) score
2018-11-1614
OAAI
Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA
2018-10-2514
OAAI
Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes
2017-12-0135
PREAI
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): Proposal for a new diagnostic paradigm
2017-11-2234
PREAI
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
2017-10-0590
OAAI
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients
2017-09-2942
OAAI