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

PARC: a phase I/II study evaluating the safety and activity of pegylated recombinant human arginase BCT-100 in relapsed/refractory cancers of children and young adults

PARC:一项 I/II 期研究,旨在评估聚乙二醇化重组人精氨酸酶 BCT-100 在儿童和青少年复发/难治性癌症中的安全性和活性。

Fenwick, Nicola; Weston, Rebekah; Wheatley, Keith; Hodgson, Jodie; Marshall, Lynley; Elliott, Martin; Makin, Guy; Ng, Antony; Brennan, Bernadette; Lowis, Stephen; Adamski, Jenny; Kilday, John Paul; Cox, Rachel; Gattens, Mike; Moore, Andrew; Trahair, Toby; Ronghe, Milind; Campbell, Martin; Campbell, Helen; Williams, Molly W; Kirby, Maria; Van Eijkelenburg, Natasha; Keely, Jennifer; Scarpa, Ugo; Stavrou, Victoria; Fultang, Livingstone; Booth, Sarah; Cheng, Paul; De Santo, Carmela; Mussai, Francis

Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect Study

Simoctocog Alfa (Nuwiq) 用于既往未接受治疗的重型血友病 A 患者:NuProtect 研究的最终结果

Liesner, Ri J; Abraham, Aby; Altisent, Carmen; Belletrutti, Mark J; Carcao, Manuel; Carvalho, Manuela; Chambost, Hervé; Chan, Anthony K C; Dubey, Leonid; Ducore, Jonathan; Gattens, Michael; Gresele, Paolo; Gruel, Yves; Guillet, Benoit; Jimenez-Yuste, Victor; Kitanovski, Lidija; Klukowska, Anna; Lohade, Sunil; Mancuso, Maria Elisa; Oldenburg, Johannes; Pavlova, Anna; Pollio, Berardino; Sigaud, Marianne; Vdovin, Vladimir; Vilchevska, Kateryna; Wu, John K M; Jansen, Martina; Belyanskaya, Larisa; Walter, Olaf; Knaub, Sigurd; Neufeld, Ellis J

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

一种用于诊断遗传性出血、血栓和血小板疾病的高通量测序检测方法

Simeoni, Ilenia; Stephens, Jonathan C; Hu, Fengyuan; Deevi, Sri V V; Megy, Karyn; Bariana, Tadbir K; Lentaigne, Claire; Schulman, Sol; Sivapalaratnam, Suthesh; Vries, Minka J A; Westbury, Sarah K; Greene, Daniel; Papadia, Sofia; Alessi, Marie-Christine; Attwood, Antony P; Ballmaier, Matthias; Baynam, Gareth; Bermejo, Emilse; Bertoli, Marta; Bray, Paul F; Bury, Loredana; Cattaneo, Marco; Collins, Peter; Daugherty, Louise C; Favier, Rémi; French, Deborah L; Furie, Bruce; Gattens, Michael; Germeshausen, Manuela; Ghevaert, Cedric; Goodeve, Anne C; Guerrero, Jose A; Hampshire, Daniel J; Hart, Daniel P; Heemskerk, Johan W M; Henskens, Yvonne M C; Hill, Marian; Hogg, Nancy; Jolley, Jennifer D; Kahr, Walter H; Kelly, Anne M; Kerr, Ron; Kostadima, Myrto; Kunishima, Shinji; Lambert, Michele P; Liesner, Ri; López, José A; Mapeta, Rutendo P; Mathias, Mary; Millar, Carolyn M; Nathwani, Amit; Neerman-Arbez, Marguerite; Nurden, Alan T; Nurden, Paquita; Othman, Maha; Peerlinck, Kathelijne; Perry, David J; Poudel, Pawan; Reitsma, Pieter; Rondina, Matthew T; Smethurst, Peter A; Stevenson, William; Szkotak, Artur; Tuna, Salih; van Geet, Christel; Whitehorn, Deborah; Wilcox, David A; Zhang, Bin; Revel-Vilk, Shoshana; Gresele, Paolo; Bellissimo, Daniel B; Penkett, Christopher J; Laffan, Michael A; Mumford, Andrew D; Rendon, Augusto; Gomez, Keith; Freson, Kathleen; Ouwehand, Willem H; Turro, Ernest

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

利用人类表型本体注释和聚类分析,揭示707例不明原因出血和血小板疾病患者的遗传缺陷。

Westbury, Sarah K; Turro, Ernest; Greene, Daniel; Lentaigne, Claire; Kelly, Anne M; Bariana, Tadbir K; Simeoni, Ilenia; Pillois, Xavier; Attwood, Antony; Austin, Steve; Jansen, Sjoert Bg; Bakchoul, Tamam; Crisp-Hihn, Abi; Erber, Wendy N; Favier, Rémi; Foad, Nicola; Gattens, Michael; Jolley, Jennifer D; Liesner, Ri; Meacham, Stuart; Millar, Carolyn M; Nurden, Alan T; Peerlinck, Kathelijne; Perry, David J; Poudel, Pawan; Schulman, Sol; Schulze, Harald; Stephens, Jonathan C; Furie, Bruce; Robinson, Peter N; van Geet, Chris; Rendon, Augusto; Gomez, Keith; Laffan, Michael A; Lambert, Michele P; Nurden, Paquita; Ouwehand, Willem H; Richardson, Sylvia; Mumford, Andrew D; Freson, Kathleen