[Adenovirus-induced liver failure in adults following allogeneic hematopoietic stem cell transplantation: a report of two cases and literature review] [0.03%]
[异基因造血干细胞移植成人受者腺病毒性肝炎致肝衰竭两例报道及文献复习]
X J Wang,N Wang,Y Yang et al.
X J Wang et al.
Human adenovirus (HAdV) hepatitis is a rare but rapidly progressive and often fatal complication following allogeneic hematopoietic stem cell transplantation. The present study reported the management of two patients with lymphoproliferativ...
[Secondary treatment-free remission in chronic myeloid leukemia in the chronic phase: a case series and literature review] [0.03%]
慢性期慢性髓性白血病无需二线治疗即获得分子学缓解的临床病例及其文献回顾
T J Huang,Y Wu,Y Wei et al.
T J Huang et al.
Data and guidelines for a second attempt at treatment-free remission (TFR) in patients with chronic myeloid leukemia in the chronic phase (CML-CP) are limited. We retrospectively analyzed the clinical data of six patients with CML-CP who at...
[Clinical characteristics of RUNX1-mutated acute myeloid leukemia patients] [0.03%]
RUNX1突变急性髓系白血病的临床特征分析
Y X Dong,W J Dai,W Q Zhang et al.
Y X Dong et al.
We retrospectively analyzed the RUNX1 mutation status and clinical characteristics of 323 newly diagnosed acute myeloid leukemia (AML) patients treated in the Second Affiliated Hospital of Anhui Medical University from February 2018 to May ...
[Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis] [0.03%]
[白细胞致死性遗传性纤溶酶原缺乏症家系研究及机制分析]
Y F Lu,D D Yu,Q Y Xu et al.
Y F Lu et al.
Objective: To investigate the molecular mechanisms underlying compound heterozygous mutations in a patient with hereditary plasminogen (PLG) deficiency. Methods: The proband presented to the First Affiliated Hospital of Wenzhou Medical Univ...
[Haploidentical hematopoietic stem cell transplantation for advanced myelodysplastic syndrome patients with recurrent genetic abnormalities] [0.03%]
haploidentical造血干细胞移植治疗复发性遗传学异常的难治性骨髓增生异常综合征患者
H T Gao,F F Tang,Y Y Zhang et al.
H T Gao et al.
Objective: To evaluate the efficacy of haploidentical hematopoietic stem cell transplantation (haplo-HSCT) in advanced myelodysplastic syndrome (MDS) patients with recurrent genetic abnormalities. Methods: We conducted a retrospective analy...
[External validation and incremental value assessment of the RR6 prognostic model in Chinese myelofibrosis patients treated with ruxolitinib: focusing on overall survival] [0.03%]
RR6预后模型在中国ruxolitinib治疗的原发性骨髓纤维化患者中的外部验证及增量价值分析：侧重总生存期终点
N N Liu,B Li,T J Qin et al.
N N Liu et al.
Objective: To validate the Response to Ruxolitinib After 6 Months (RR6) prognostic model in Chinese patients with myelofibrosis (MF) treated with ruxolitinib and assess its incremental prognostic value when integrated with high molecular ri...
[The value of T-cell receptor gene rearrangement in the auxiliary diagnosis of T-cell large granular lymphocytic leukemia] [0.03%]
T细胞受体基因重排在T细胞大颗粒淋巴细胞白血病辅助诊断中价值探讨
L Y Zhu,H M Jin,Y J Wu et al.
L Y Zhu et al.
Objective: To explore the characteristics and auxiliary diagnostic value of T-cell receptor (TCR) gene rearrangement in T-cell abnormal clonal diseases, including T-cell large granular lymphocytic leukemia (T-LGLL) . Methods: Altogether, 10...
[Comparative analysis of long-term efficacy between the CCCG-ALL-2015 and CCLG-ALL-2008 protocols in adolescents with acute lymphoblastic leukemia] [0.03%]
CCCG-ALL-2015方案与CCLG-ALL-2008方案治疗青少年急性淋巴细胞白血病的远期疗效比较分析
S Lin,H Lyu,X Y Li et al.
S Lin et al.
Objective: To compare the long-term efficacy and safety of the CCCG-ALL-2015 and CCLG-ALL-2008 protocols in treating adolescents and older children (aged ≥10 years) with acute lymphoblastic leukemia (ALL) and explore the key factors affect...
[Clinical characteristics and prognosis of myelodysplastic neoplasms with chromosome 1 abnormalities] [0.03%]
[1号染色体异常骨髓增生异常肿瘤的临床特点和预后]
Z L Kuang,B Li,T J Qin et al.
Z L Kuang et al.
Objective: To characterize the clinical and molecular features and evaluate the prognostic outcomes of patients with myelodysplastic neoplasms (MDS) with chromosome 1 abnormalities. Methods: We retrospectively analyzed 1 498 newly diagnosed...
R Fu,H Liu
R Fu
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired clonal disorder of hematopoietic stem cells with diverse clinical manifestations, making it susceptible to missed diagnosis or misdiagnosis. Early clinical screening through mult...