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

Molecular genetic testing in von Willebrand disease: past, present, and beyond

血管性血友病分子遗传学检测:过去、现在和未来

Seidizadeh, Omid; Lillicrap, David

Factor VIII in vitro bioequivalence of denecimig (Mim8) hemostatic effect by thrombin generation assays

通过凝血酶生成试验评估因子VIII与denecimig(Mim8)的体外生物等效性止血作用

Lund, Jacob; Ezban, Mirella; Jensen, Kasper; Lillicrap, David

Translational insights from nonclinical studies of AAV gene therapies for hemophilia: mechanisms underpinning variability and durability of gene expression

来自非临床研究中AAV基因疗法治疗血友病的转化性见解:基因表达变异性和持久性的潜在机制

Fong, Sylvia; Swystun, Laura L; Batty, Paul; Lillicrap, David

Mild or moderate hemophilia is not always a mild or moderate bleeding disorder: Back to the clinical phenotype

轻度或中度血友病并不总是轻度或中度出血性疾病:回到临床表型

Rodeghiero, Francesco; Ghiotto, Lisanna; Pontalto, Luca; Casini, Alessandro; Castaman, Giancarlo; Abdul-Kadir, Rezan; Berntorp, Erik; Bodó, Imre; Degenaar-Dujardin, Manon; Fijnvandraat, Karin; Gresele, Paolo; Key, Nigel S; Lassila, Riitta; Leebeek, Frank W G; Lillicrap, David; Makris, Mike; Meijer, Stephan; Mezzano, Diego; Noris, Patrizia; Pabinger, Ingrid; Ragni, Margaret V; Silva, David; Srivastava, Alok; Tosetto, Alberto; Windyga, Jerzy; Zieger, Barbara

Regulation of immune responses to therapeutic factor VIII by transplacental delivery of Fc-fused immunodominant factor VIII domains or peptides

通过胎盘递送Fc融合的免疫优势因子VIII结构域或肽段来调节对治疗性因子VIII的免疫反应

Reyes-Ruiz, Alejandra; Delignat, Sandrine; Azam, Aurélien; Daventure, Victoria; Dourthe, Leslie; Mimoun, Angelina; McCluskey, Geneviève; Georgescu, Maria T; Lillicrap, David; Dimitrov, Jordan D; Lacroix-Desmazes, Sebastien

Effect of age on ISTH-BAT scores and low VWF diagnosis in the Zimmerman Program

年龄对 ITH-BAT 评分和 Zimmerman 项目中低 VWF 诊断的影响

Atiq, Ferdows; Christopherson, Pamela A; Doherty, Dearbhla; Hulshof, Anne-Marije; Haberichter, Sandra L; Flood, Veronica H; Lavin, Michelle; O'Connell, Niamh M; Ryan, Kevin; Byrne, Mary; Grabell, Julie; James, Paula D; Lillicrap, David; Montgomery, Robert R; Di Paola, Jorge; O'Donnell, James S

Identification of multiple novel procoagulant plasma ligands for stabilin-2.

鉴定出多种新型促凝血血浆配体,用于稳定蛋白-2。

Underwood Mary, Da Veiga Leprevost Felipe, Basrur Venkatesha, Nesvizhskii Alexey I, Rawley Orla, Golden Krista, Emmer Brian, Lillicrap David, Desch Karl

Factor XIII deficiency due to compound heterozygosity for 2 F13A1 variants

由于两种 F13A1 变异体的复合杂合性导致的 XIII 因子缺乏症

Odame, Jodie; Malcolmson, Caroline; Wakefield, Cindy; Bourque, Tammy; Lillicrap, David; Rawley, Orla; Bowman, Mackenzie; Carcao, Manuel; Bouskill, Vanessa

Large deletions in the F8 gene predict immune tolerance induction failure in people with severe hemophilia A

F8基因的大片段缺失预示着重度A型血友病患者免疫耐受诱导失败。

Oomen, Ilja; Abdi, Amal; Broer, Linda; Camelo, Ricardo M; Callado, Fábia M R A; Carvalho, Luany E M; Calcaterra, Ilenia L; Carcao, Manuel; Castaman, Giancarlo; Eikenboom, Jeroen C J; Fischer, Kathelijn; Franco, Vivian K B; Geissler, Judy; Kuijpers, Taco W; Leebeek, Frank W G; Lillicrap, David; Lorenzato, Cláudia S; Mancuso, Maria Elisa; Matino, Davide; Di Minno, Matteo N D; Mo, Aomei; Mohseny, Alex B; Nagelkerke, Sietse Q; Oldenburg, Johannes; Rezende, Suely Meireles; Rivard, Georges-Etienne; Rydz, Natalia; Schols, Saskia E M; Tanck, Michael W T; Voorberg, Jan; Fijnvandraat, Karin; Gouw, Samantha C

Genomic testing for bleeding disorders (GT4BD): protocol for a randomised controlled trial evaluating the introduction of whole genome sequencing early in the diagnostic pathway for patients with inherited bleeding disorders as compared with standard of care

出血性疾病基因组检测(GT4BD):一项随机对照试验方案,旨在评估在遗传性出血性疾病患者诊断流程早期引入全基因组测序与标准治疗相比的效果。

Chaigneau, Megan; Bowman, Mackenzie; Grabell, Julie; Conboy, Megan; Johnson, Ana; Thorpe, Kevin; Guerin, Andrea; Dinchong, Rachelle; Paterson, Andrew; Good, David; Mahar, Alyson; Callum, Jeannie; Wheaton, Laura; Leung, Jennifer; Khalife, Roy; Sholzberg, Michelle; Lillicrap, David; James, Paula D