A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AML [0.03%]
一例复杂核型伴正常整倍体高超二倍体的成人AML病例及其疗效和复发研究
Abdulsamad Wafa,Suher ALmedania,Abdulmunim Aljapawe et al.
Abdulsamad Wafa et al.
Background: Chromosomal abnormalities are diagnostic and prognostic key factors in acute myeloid leukemia (AML) patients, as they play a central role for risk stratification algorithms. High hyperdiploidy (HH), a rare cyt...
Case Reports
BMC hematology. 2018 Aug 31:18:21. DOI:10.1186/s12878-018-0114-3 2018
Useful clinical features and hematological parameters for the diagnosis of dengue infection in patients with acute febrile illness: a retrospective study [0.03%]
急性发热患者登革病毒感染的临床特征及血液学参数的回顾性研究
Juthatip Chaloemwong,Adisak Tantiworawit,Thanawat Rattanathammethee et al.
Juthatip Chaloemwong et al.
Background: Dengue infection patients are presented with acute febrile illness. Clinical presentations may mimic other infections. The serology for definite diagnosis is costly and inaccessible in many hospitals. We sough...
Rapid access clinic for unexplained lymphadenopathy and suspected malignancy: prospective analysis of 1000 patients [0.03%]
不明原因淋巴结病和可疑恶性肿瘤的快速诊疗诊所：1000例前瞻性分析
Andrea Kühnl,David Cunningham,Margaret Hutka et al.
Andrea Kühnl et al.
Background: In patients presenting with peripheral lymphadenopathy, it is critical to effectively identify those with underlying cancer who require urgent specialist care. ...
Rare and unusual case of anti-factor XI antibodies in patient with plasma cell leukemia [0.03%]
一例浆细胞白血病患者的抗因子XI抗体罕见病例报告
Jean Uwingabiye,Hafid Zahid,Mohamed El Amrani et al.
Jean Uwingabiye et al.
Background: The acquired inhibitors of coagulation have been observed in very rare cases of monoclonal gammopathies. We report a very rare case of anti-factor XI antibodies in patient with plasma cell leukemia (PCL). ...
Case Reports
BMC hematology. 2018 Aug 10:18:18. DOI:10.1186/s12878-018-0100-9 2018
Identification of a novel mutation in the factor VIII gene causing severe haemophilia A [0.03%]
FⅧ基因新型突变导致严重甲型血友病的鉴定
S K Nissen,A L Laursen,L H Poulsen et al.
S K Nissen et al.
Background: Deficiency in coagulation factor VIII encoded by F8 results in the X-linked recessive bleeding disorder haemophilia A (HEMA). Here we describe the identification of a novel variant in the factor VIII gene, F8,...
Case Reports
BMC hematology. 2018 Jul 31:18:17. DOI:10.1186/s12878-018-0113-4 2018
Demographic characteristics of blood and blood components transfusion recipients and pattern of blood utilization in a tertiary health institution in southern Nigeria [0.03%]
尼日利亚南部一家三级保健机构输血和血液成分受者的人口统计特征及血液利用模式
Henshaw Uchechi Okoroiwu,Ifeyinwa Maryann Okafor
Henshaw Uchechi Okoroiwu
Background: An insight into the utilization pattern helps in future planning of blood drive. This study was conducted to describe the demographic characteristics of the transfusion recipients and pattern of blood and bloo...
Hematological profile of pregnant women at St. Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia [0.03%]
埃塞俄比亚亚的斯亚贝巴圣保罗医院 Millennium 大学医学院孕妇血液检查结果
Angesom Gebreweld,Delayehu Bekele,Aster Tsegaye
Angesom Gebreweld
Background: In pregnancy, hematological changes occur in order to meet the demands of the developing fetus and placenta, with major alterations in blood volume. Abnormal hematological profile affects pregnancy and its out...
Anemia and associated factors among children aged 6-23 months in Damot Sore District, Wolaita Zone, South Ethiopia [0.03%]
埃塞俄比亚沃尔亚塔区达莫特索雷 district 6-23 月龄儿童贫血现状及影响因素分析
Bereket Geze Malako,Melese Sinaga Teshome,Tefera Belachew
Bereket Geze Malako
Background: Anemia affects a significant part of the population in nearly every country in the globe. Iron requirements are greatest at ages 6-23 months when growth is extremely rapid and critically essential in critical ...
Adapting medical guidelines to be patient-centered using a patient-driven process for individuals with sickle cell disease and their caregivers [0.03%]
一种以患者为中心的方法：通过患者驱动的过程使镰状细胞病患者的医疗指南更具个性化
Robert Michael Cronin,Tilicia L Mayo-Gamble,Sarah-Jo Stimpson et al.
Robert Michael Cronin et al.
Background: Evidence-based guidelines for sickle cell disease (SCD) health maintenance and management have been developed for primary health care providers, but not for individuals with SCD. To improve the quality of care...
Experimental folate deficiency in human subjects: what is the influence of vitamin C status on time taken to develop megaloblastic anaemia? [0.03%]
实验性叶酸缺乏对人体受试者的影响：维生素C状态对巨幼红细胞性贫血发病时间的作用是什么？
Paul Henry Golding
Paul Henry Golding
Background: In 1962 Victor Herbert developed megaloblastic anaemia four months after commencing a severely folate-deficient diet whereas, in his self-experiment 50 years later, this author took 19 months to fully deplete ...