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

Wolf Presence near a Temporary Sheep Pasture in Flanders: A Descriptive Camera-Trap Study

弗兰德斯临时牧羊场附近狼群活动:一项描述性相机陷阱研究

Driessen, Bert; Pellens, Lore; Bollen, Celine; Tavernier, Jasper; Freson, Louis

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy

小核RNA基因RNU2-2的突变会导致严重的神经发育障碍,并伴有明显的癫痫症状。

Greene, Daniel; De Wispelaere, Koenraad; Lees, Jon; Codina-Solà, Marta; Jensson, Brynjar O; Hales, Emma; Katrinecz, Andrea; Nieto Molina, Esther; Pascoal, Sonia; Pfundt, Rolph; Schot, Rachel; Sevilla Porras, Marta; Sleutels, Frank; Valenzuela, Irene; Wijngaard, Robin; Arroyo Carrera, Ignacio; Atton, Giles; Casas-Alba, Didac; Donnelly, Deirdre; Duat Rodríguez, Anna; Fernández Garoz, Bárbara; Foulds, Nicola; García-Navas Núñez, Deyanira; González Alguacil, Elena; Jarvis, Joanna; Kant, Sarina G; Madrigal Bajo, Irene; Martinez-Monseny, Antonio F; McKee, Shane; Ortiz Cabrera, Nelmar Valentina; Rodríguez-Revenga Bodi, Laia; Sariego Jamardo, Andrea; Stefansson, Kari; Sulem, Patrick; Suri, Mohnish; Van Karnebeek, Clara; Vasudevan, Pradeep; Vega Pajares, Ana Isabel; Carracedo, Ángel; Engelen, Marc; Lapunzina, Pablo; Morgan, Natasha P; Morte, Beatriz; Rump, Patrick; Stirrups, Kathy; Tizzano, Eduardo F; Barakat, Tahsin Stefan; O'Donoghue, Michael; Pérez-Jurado, Luis Alberto; Freson, Kathleen; Mumford, Andrew D; Turro, Ernest

Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy)

生殖系 RUNX1 缺陷(伴有髓系恶性肿瘤的家族性血小板疾病)急性髓系白血病的疾病特征和预后

Ernst, Martijn P T; Versluis, Jurjen; Valk, Peter J M; Bierings, Marc; Tamminga, Rienk Y J; Hooimeijer, Louise H; Döhner, Konstanze; Gresele, Paolo; Tawana, Kiran; Langemeijer, Saskia M C; Van der Reijden, Bert A; Podgornik, Helena; Sever, Matjaz; Tvedt, Tor H A; Vulliamy, Tom; Fitzgibbon, Jude; Dokal, Inderjeet; Baliakas, Panagiotis; Bastida, José M; Pohlkamp, Christian; Haferlach, Torsten; Larcher, Lise; Soulier, Jean; Schutgens, Roger E G; Freson, Kathleen; Duployez, Nicolas; Löwenberg, Bob; Ericson, Katrin; Cammenga, Jörg; Ripperger, Tim; Raaijmakers, Marc H G P

Transcriptome profiling of megakaryocytes and platelets: Application to GP9- and IKZF5-related thrombocytopenia

巨核细胞和血小板转录组分析:在GP9和IKZF5相关血小板减少症中的应用

De Wispelaere, Koenraad; Ver Donck, Fabienne; Ramaekers, Kato; Thys, Chantal; Eto, Koji; Labarque, Veerle; Turro, Ernest; Freson, Kathleen

Implementation and clinical utility of multigene panels for bleeding, platelet, and thrombotic disorders

多基因检测在出血、血小板和血栓性疾病中的应用及临床价值

Ramanan, Radha; Verstraete, Andreas; Van Laer, Christine; Freson, Kathleen

Clinical utility of panel-based genetic sequencing for von Willebrand disease

基于基因组测序的血管性血友病临床应用价值

Ramanan, Radha; Van Laer, Christine; Baert, Sarissa; Kint, Cyrielle; Van Geet, Chris; Van Thillo, Quentin; Verhamme, Peter; Vanassche, Thomas; McFadyen, James D; Perkins, Andrew C; Tran, Huyen A; Labarque, Veerle; Freson, Kathleen

Illustrated capsules from the Advanced Course in Platelet Research

血小板研究高级课程的图文概要

Di Buduo, Christian Andrea; Abbonante, Vittorio; Malara, Alessandro; Balduini, Alessandra; Waller, Amie K; Watson, Steve P; Martin, Eleyna M; Bridge, Lloyd; Gibbins, Jonathan; Hers, Ingeborg; Masson, Claire; Eckly, Anita; Poulter, Natalie S; Martínez-García, Beatriz; Aguila, Sonia; Gresele, Paolo; Momi, Stefania; Amstrong, Paul; Rondina, Matthew; Troitiño, Sara; García, Ángel; Bastida, José M; Quilez, Ana Marín; Fuentes, Ana Sánchez; Rivera, José; Torres-Ruiz, Raul; Ojeda-Walczuk, Paula; Morgan, Neil V; Morena, Belen de la; Ramaekers, Kato; Tran, My; De Wispelaere, Koen; Freson, Kathleen; Bergmeier, Wolfgang; Greinacher, Andreas; He, Fan; Oh, Stephen; Di Paola, Jorge; Semple, John W; Lozano, María L; Llamas, Pilar; Ward, Chris

Epidemiology of Venous Thromboembolism in Belgium: A Cohort Study

比利时静脉血栓栓塞症的流行病学:一项队列研究

Verstraete, Andreas; Cauwenberghs, Nicholas; Calhori, Shayan; Van Durme, Joren; Freson, Kathleen; Verhamme, Peter; Kuznetsova, Tatiana; Vanassche, Thomas

Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders

U4 snRNA基因RNU4-2的突变会导致最常见的单基因神经发育障碍之一。

Greene, Daniel; Thys, Chantal; Berry, Ian R; Jarvis, Joanna; Ortibus, Els; Mumford, Andrew D; Freson, Kathleen; Turro, Ernest

Prospective, international, multisite comparison of platelet isolation techniques for genome-wide transcriptomics: communication from the SSC of the ISTH

国际血栓与止血学会(ISTH)科学标准委员会(SSC)的报告:前瞻性、国际性、多中心血小板分离技术在全基因组转录组学中的比较研究。

Meenakshi Banerjee ,Jesse W Rowley ,Chris J Stubben ,Neal D Tolley ,Kathleen Freson ,Benjamin Nelson ,Béla Nagy Jr ,Zsolt Fejes ,Antoinette M Blair ,Ernest Turro ,Paolo Gresele ,Giulia Ciarrocca Taranta ,Loredana Bury ,Emanuela Falcinelli ,Marie Lordkipanidzé ,Marie-Christine Alessi ,Andrew D Johnson ,Tamam Bakchoul ,Sofia Ramstrom ,Mattia Frontini ,Marina Camera ,Marta Brambilla ,Robert A Campbell ,Matthew T Rondina