Vidya Nagrale,Ahmad Alduaij,Ahmad Alrustamani et al.
Vidya Nagrale et al.
Improving real-world myeloma patient access to whole body MRI through "open-access" knowledge sharing: The UK experience [0.03%]
通过"开放获取"知识共享提高真实世界骨髓瘤患者全身MRI检查的可及性：英国的经验
Martin F Kaiser,Kevin Boyd,Dow-Mu Koh et al.
Martin F Kaiser et al.
Marginal zone lymphoma expression of histidine-rich glycoprotein correlates with improved survival [0.03%]
边缘区淋巴瘤中富含组氨酸糖蛋白的表达与生存期改善有关
Tor Persson Skare,Elin Sjöberg,Mattias Berglund et al.
Tor Persson Skare et al.
Purpose: The abundant hepatocyte-expressed plasma protein histidine-rich glycoprotein (HRG) enhances antitumor immunity by polarizing inflammatory and immune cells in several mouse models, however, the clinical relevance ...
Hypertension in patients with hereditary thrombotic thrombocytopenic purpura [0.03%]
遗传性血栓性血小板减少性紫癜患者的高血压病症
Azra Borogovac,Erika Tarasco,Johanna A Kremer Hovinga et al.
Azra Borogovac et al.
Acute dilated cardiomyopathy in the setting of catastrophic antiphospholipid syndrome and thrombotic microangiopathy: A case series and review [0.03%]
抗磷脂综合征伴发微血管血栓形成的急性扩张型心肌病：病例分析及文献回顾
Melody Hermel,David Hermel,Saif Azam et al.
Melody Hermel et al.
Catastrophic antiphospholipid antibody syndrome (CAPS) is a rare form of antiphospholipid syndrome, an autoimmune condition characterized by vascular thromboses, pregnancy loss, and antiphospholipid (aPL) antibodies. Diagnosis of CAPS relie...
Paroxysmal nocturnal hemoglobinuria-phenotype cells predict a good response to eltrombopag in patients with refractory aplastic anemia [0.03%]
阵发性夜间血红蛋白尿表型细胞可预测难治性再生障碍性贫血患者对艾曲波帕的反应良好
Ken Ishiyama,Keijiro Sato,Tatsuya Imi et al.
Ken Ishiyama et al.
To identify factors affecting responsiveness to eltrombopag (EPAG), we retrospectively analyzed 38 aplastic anemia patients treated with EPAG who were refractory (n = 29) or showed an inadequate response (n = 9) to conventional therapies. T...
Zufit Hexner-Erlichman,Joanne Yacobovich,Philippe Trougouboff et al.
Zufit Hexner-Erlichman et al.
Autoimmune myelofibrosis (AIMF) is an uncommon cause of myelofibrosis associated with favorable outcome. Primary AIMF, AIMF without a known systemic autoimmune disorder, has been described in adults, but never in children. Here, we present,...
Case Reports
EJHaem. 2020 Jun 28;1(1):304-308. DOI:10.1002/jha2.38 2020
Anthony P Williams,Jessica Bate,Rachael Brooks et al.
Anthony P Williams et al.
Although survival rates for pediatric acute lymphoblastic leukemia are now excellent, this is at the expense of prolonged chemotherapy regimens. We report the long-term immune effects in children treated according to the UK Medical Research...
Diagnostic and molecular testing patterns in patients with newly diagnosed acute myeloid leukemia in the Connect® MDS/AML Disease Registry [0.03%]
美国一项急性髓系细胞白血病登记研究中的诊断及分子检测模式分析
Daniel A Pollyea,Tracy I George,Mehrdad Abedi et al.
Daniel A Pollyea et al.
Diagnostic and molecular genetic testing are key in advancing the treatment of acute myeloid leukemia (AML), yet little is known about testing patterns outside of clinical trials, especially in older patients. We analyzed diagnostic and mol...
Stomatocytes and macrothrombocytopenia: A blood film for a rare disease [0.03%]
stomatocyte和macrothrombocytopenia：罕见病的血涂片
Alessandro La Rosa,Erica Ricci,Francesca Scuderi et al.
Alessandro La Rosa et al.