日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

APOLD1 loss causes endothelial dysfunction involving cell junctions, cytoskeletal architecture, and Weibel-Palade bodies, while disrupting hemostasis

APOLD1 缺失会导致涉及细胞连接、细胞骨架结构和 Weibel-Palade 体的内皮功能障碍,同时破坏止血

Simon Stritt, Paquita Nurden, Alan T Nurden, Jean-François Schved, Jean-Claude Bordet, Maguelonne Roux, Marie-Christine Alessi, David-Alexandre Trégouët, Taija Mäkinen, Muriel Giansily-Blaizot

The GPIIb-IIIa defect of platelets in Glanzmann thrombasthenia

格氏血小板无力症中的血小板GPIIb-IIIa缺陷

Nurden, Alan T

A single F153Sβ3 mutation causes constitutive integrin αIIbβ3 activation in a variant form of Glanzmann thrombasthenia

单个 F153Sβ3 突变导致格氏血小板无力症变异型中整合素 αIIbβ3 的组成型激活。

Koukouritaki, Sevasti B; Thinn, Aye Myat M; Ashworth, Katrina J; Fang, Juan; Slater, Haley S; Du, Lily M; Nguyen, Huong Thi Thu; Pillois, Xavier; Nurden, Alan T; Ng, Christopher J; Di Paola, Jorge; Zhu, Jieqing; Wilcox, David A

Inherited platelet diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy

血小板计数正常的遗传性血小板疾病:表型、基因型和诊断策略

Nurden, Paquita; Stritt, Simon; Favier, Remi; Nurden, Alan T

Profiling the Genetic and Molecular Characteristics of Glanzmann Thrombasthenia: Can It Guide Current and Future Therapies?

分析格氏血小板无力症的遗传和分子特征:能否指导当前和未来的治疗?

Nurden, Alan

Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome

灰血小板综合征中免疫失调和颗粒缺陷的新表现

Sims, Matthew C; Mayer, Louisa; Collins, Janine H; Bariana, Tadbir K; Megy, Karyn; Lavenu-Bombled, Cecile; Seyres, Denis; Kollipara, Laxmikanth; Burden, Frances S; Greene, Daniel; Lee, Dave; Rodriguez-Romera, Antonio; Alessi, Marie-Christine; Astle, William J; Bahou, Wadie F; Bury, Loredana; Chalmers, Elizabeth; Da Silva, Rachael; De Candia, Erica; Deevi, Sri V V; Farrow, Samantha; Gomez, Keith; Grassi, Luigi; Greinacher, Andreas; Gresele, Paolo; Hart, Dan; Hurtaud, Marie-Françoise; Kelly, Anne M; Kerr, Ron; Le Quellec, Sandra; Leblanc, Thierry; Leinøe, Eva B; Mapeta, Rutendo; McKinney, Harriet; Michelson, Alan D; Morais, Sara; Nugent, Diane; Papadia, Sofia; Park, Soo J; Pasi, John; Podda, Gian Marco; Poon, Man-Chiu; Reed, Rachel; Sekhar, Mallika; Shalev, Hanna; Sivapalaratnam, Suthesh; Steinberg-Shemer, Orna; Stephens, Jonathan C; Tait, Robert C; Turro, Ernest; Wu, John K M; Zieger, Barbara; Kuijpers, Taco W; Whetton, Anthony D; Sickmann, Albert; Freson, Kathleen; Downes, Kate; Erber, Wendy N; Frontini, Mattia; Nurden, Paquita; Ouwehand, Willem H; Favier, Remi; Guerrero, Jose A

Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study

针对遗传性血小板疾病患者手术相关静脉血栓栓塞风险的抗血栓预防:SPATA-DVT 研究

Paciullo, Francesco; Bury, Loredana; Noris, Patrizia; Falcinelli, Emanuela; Melazzini, Federica; Orsini, Sara; Zaninetti, Carlo; Abdul-Kadir, Rezan; Obeng-Tuudah, Deborah; Heller, Paula G; Glembotsky, Ana C; Fabris, Fabrizio; Rivera, Jose; Lozano, Maria Luisa; Butta, Nora; Favier, Remi; Cid, Ana Rosa; Fouassier, Marc; Podda, Gian Marco; Santoro, Cristina; Grandone, Elvira; Henskens, Yvonne; Nurden, Paquita; Zieger, Barbara; Cuker, Adam; Devreese, Katrien; Tosetto, Alberto; De Candia, Erica; Dupuis, Arnaud; Miyazaki, Koji; Othman, Maha; Gresele, Paolo

Inherited thrombocytopenias: history, advances and perspectives

遗传性血小板减少症:历史、进展和展望

Nurden, Alan T; Nurden, Paquita

Is the mysterious platelet receptor GPV an unsuspected major target for platelet autoantibodies?

神秘的血小板受体GPV是否是血小板自身抗体的一个意想不到的主要靶点?

Nurden, Paquita; Nurden, Alan T

Defective Zn2+ homeostasis in mouse and human platelets with α- and δ-storage pool diseases

患有 α 和 δ 储存池疾病的小鼠和人类血小板中 Zn2+ 稳态缺陷

Sanjeev Kiran Gotru, Johanna P van Geffen, Magdolna Nagy, Elmina Mammadova-Bach, Julia Eilenberger, Julia Volz, Georgi Manukjan, Harald Schulze, Leonard Wagner, Stefan Eber, Christian Schambeck, Carsten Deppermann, Sanne Brouns, Paquita Nurden, Andreas Greinacher, Ulrich Sachs, Bernhard Nieswandt, H