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hematological disease
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  血液病
     Objective To reseach the condition of human parvovirus B19 (HPVB19) infection in children's hematological disease (leukemia, idiopathic thrombcytopenic purpura, anaemia) and the relationship between them.
     目的:了解儿童血液病人(白血病、血小板减少性紫癜、贫血)细小病毒B19(Human parvovirus B19,HPVB19)感染的状况及其关系。
短句来源
     Clinical Characteristics in 18 Cases of Sever Pneumonia after Allogeneic Hematopoietic Stem Cell Transplantation for Malignant Hematological Disease
     恶性血液病异基因造血干细胞移植后并发重症肺炎18例临床分析
短句来源
     All of 4 patients with CML at blast crisis stage had positive expresion of WT1. As contrast, neither 10 volunteers, nor 10 patients with no hematological disease were WT1 positive.
     16例慢性粒细胞白血病 (CML )中的 7例 (44 % ) WT1表达阳性 ,其中 4例急变者全部为阳性 ,10名正常人及 10例非血液病患者的 WT1表达阴性。
短句来源
     T Cell Clonality in Hematological Disease and Autoimmune Disease Using Analysis of TCR Vβ Gene Repertoire
     应用TCR Vβ基因谱分析血液病与免疫性疾病的T细胞克隆性
短句来源
     Conclusion The infection of HPVB19 may associate with the children's hematological disease. The infection of HPVB19 often occurs in children with leucocythemia treated by chemotherapy, and causes the bone marrow depression and chronic anaemia.
     结论:HPVB19感染可能与儿童血液病发病有关,进行化疗时白血病患儿易继发HPVB19感染,并可致骨髓抑制和慢性贫血。
短句来源
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  血液系统疾病
     Results:158 cases(43.2%)are diagnosed as disease of hematological system,in which 75 cases are leukemia and the other 83 cases consist of other hematological disease;
     结果:诊断血液系统疾病患者158例(43.2%),其中各种白血病75例,其它血液系统疾病83例;
短句来源
     Application of CIK cells to malignant hematological disease
     CIK细胞在恶性血液系统疾病中的应用研究
短句来源
     To monitor engraftment after allogenic bone marrow transplantation (Allo-BMT) in treatment hematological disease and genetic diseases,cellular in situ polymerase chain reaction (in situ PCR) was carried out on peripheral blood and marrow cells from 2 female patients with acute myelogenous leukemia (AML) after marrow ablative therapy followed by male donor marrow infusion,by use of human Y chromosome specific primer pairs Y3 and Y4,with direct incorporating nonisotopic nucleotide Dig-11-dUTP.
     为监测异性别骨髓移植(BMT)治疗某些血液系统疾病和遗传性疾病的植入状态,利用人Y染色体特异性片段扩增引物Y3、Y4,采用非放射性核苷类似物Dig-11-dUTP直接掺入法,对2例急性粒细胞性白细胞进行原位聚合酶链反应(insituPCR)。
短句来源
     Objective To study the feasibility and clinical outcome of granulocyte-colony stimulating factor (G-CSF) mobilized allogeneic bone marrow (G-BM) plus G-CSF mobilized peripheral blood stem cells (G-PBSC) transplantation for malignant hematological disease.
     目的 探讨粒细胞集落刺激因子 (G CSF)动员的异基因骨髓与外周血干细胞混合移植治疗血液系统疾病的可行性与疗效。 方法 供者给予G CSF连续 4~ 6天皮下注射 ,注射后第 3天从髂后上嵴抽取G CSF动员的骨髓血 ,第 4天开始取外周血干细胞。
短句来源
     ConclusionsOur data may have great significance for the empirical use of antimicrobial agents in the treatment of infections in patients with hematological disease.
     结论本研究结果对血液系统疾病合并感染患者的经验性用药有重要的参考价值。
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  “hematological disease”译为未确定词的双语例句
     Rapid Amplification of cDNA Ends and Its Application in Hematological Disease
     cDNA末端快速扩增技术及其在血液疾病上的应用
短句来源
     MethodsA total of 355 bacterial strains were isolated from 270 patients with hematological disease from January 2000 to June 2004.Antimicrobial susceptibility testing was done by Kirby-Bauer method and the data was analyzed by WHONET 5.2 software.
     方法收集我院血液科2000年1月—2004年6月的住院患者临床分离菌株用Kirby-Bauer法进行药敏试验,并应用WHONET5.2软件分析数据。
短句来源
     Waldenstrm′s macroglobulinemia (WM) is one of malignant hematological disease on account of abnormal proliferation of B lymphocyte clone and the pathologic cells of WM possess ability to secrete monoclonal immunoglobulin M. In this study, the diagnosis and morphological characteristics of 2 patients with WM were analyzed.
     Waldenstr m巨球蛋白血症 (WM)是由B淋巴细胞克隆异常增殖所致的血液系统恶性肿瘤 ,其病理细胞具有分泌单克隆免疫球蛋白M的功能。 本研究对 2例WM患者的诊断经过及形态学特点进行了分析。
短句来源
     In this paper, we had observed neutrophils with ring shaped nuclei in bone marrow of 72 patients with various kinds of hematological disease and 26 patients with infectlous granulocytosis. Neutrophils with ring shaped nuclei was found in 20 of 21 patients with chronic myelocytic leukemia(CML),X0.08±0. 52;
     本文对72例不同血液疾病和26例感染性疾病骨髓中环状核粒细胞进行观察,结果表明慢粒21例中出现环状核粒细胞20例,环状核粒细胞比值x0.80±0.52。
短句来源
     In order to get clinical information about safety and feasibility of successively double autologous hemopoietic stem cell transplants (SD-AHSCT) in malignant hematological disease patients, the complications and hematological reconstitution after SD-AHSCT in 20 patients were analyzed retrospectively.
     为了解自体外周血与骨髓造血干 祖细胞先后双次移植 (SD AHSCT)的安全性与可行性 ,对我科开展的 2 0例SD AHSCT的移植相关并发症及造血重建情况进行了回顾性分析。
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  hematological disease
The cardiotoxicity of adriamycin limits its clinical use as a powerful drug for solid tumors and malignant hematological disease.
      
PNH is a very rare autoimmune hematological disease.
      
Sibling cases of Mycobacterium avium complex disease associated with hematological disease
      
In addition, SCID mice readily support normal and pathologic human hematopoiesis differentiation and is useful for testing innovative hematological disease therapy.
      
Skeletal high turnover in patients with osteoporosis and systemic hematological disease
      
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Recent change of blood pictures by self-control and clinical observation before and after fetal liver cell suspension infusion (FLI) in the treatment of 46 patients with hematological diseases for 130 person-times in recent two years were reported.There were 64 episodes fo FLI in chemotherapy group. Two weeks after FLI, WBC and BPC rose quickly to more than 20% in 75% and 70% of cases respec-were significant differences of WBC and BPC when compared to the self-control group with chemotherapy only(P<0.001),but...

Recent change of blood pictures by self-control and clinical observation before and after fetal liver cell suspension infusion (FLI) in the treatment of 46 patients with hematological diseases for 130 person-times in recent two years were reported.There were 64 episodes fo FLI in chemotherapy group. Two weeks after FLI, WBC and BPC rose quickly to more than 20% in 75% and 70% of cases respec-were significant differences of WBC and BPC when compared to the self-control group with chemotherapy only(P<0.001),but the change of reticulocytes tively. There was mild. The clinical condition, hemogram and marrow picture of two patients with refractory ALL in the late improved by FLI after the lash-chemotherapy with high dosage (1000mg) of MTX. FLI could also rise blood pictures in the group of hematic tonic diseases after no cure of conventional treatment. Among those, the therapuetc effect of FLI for acute, agranulocytosis was dramatic and rapid. It is possible that FLI play a role of peculiar effect.One out of 3 cases with pure red cell aplasia returned to remission for 25 months after self-FLI. It seems the autogenic FLI is more efficient than allogenic FLI. A patient with acute myelofibrosis was treated with routine cure and FL1 of 17 times for 20 months, his blood picture revealed mild temporary improvement, while he returned to marked remission after the treatment with vitamin D3. It showed that FLI cooperate with relative cure would make more efficienty.The response of FLI in aplastic anemia, refractory anemia and idiopathic thrombocytopenic purpura was not marked and persistent. This results may relate to their special pathogenesis.The number of infusion cells and ABO blood group were not relate to thera-puetic effect. The different blood group between the donor and recipient for FLI is safe and no side effect. We infer that hormonal factors are seemingly more important than cell factors in the major mechanism of FLI effect.

用自身对比法分析观察血液病46例,FLI30例次治疗前后血象及临床疗效。化疗组FLI后两周WBC及BPC上升20%以上者分别为75%及70.3%;与自身单纯化疗相比相差非常显著(P<0.001);但Ret改变不明显。升血药组中急性粒缺疗效显著迅速,纯红再障一例经自身FLI后缓解两年未复发。AMF一例FLI17次仅有短暂血象改善,后加用维生D_3治疗后缓解15个月。慢性再障,难治性贫血及ITP疗效不显著不持久。FLI的细胞数量与疗效无明显相关、供受者ABO血型不同的FLI无不良反应。FLI疗效机制中体液因素比细胞因素似更重要。

This paper reported 3,263 hospitalized cases with hematological diseases in the first affiliated hospital to Sun Yat sen university from Jan, 1960 to Dec, 1986, accounting for 5.73% of all patients of internal medicine during the same period. They were divided into 23 groups of which 6 showed higher incidence of acutele ukemia (21.91%), aplastic anemia (14.13%), chronic granulocytic leukemia (11.55%), idiopathic thrombocytopenic anemia (9.29%), malignant lymphoma (9.13%) and iron deficiency anemia (7.11%)...

This paper reported 3,263 hospitalized cases with hematological diseases in the first affiliated hospital to Sun Yat sen university from Jan, 1960 to Dec, 1986, accounting for 5.73% of all patients of internal medicine during the same period. They were divided into 23 groups of which 6 showed higher incidence of acutele ukemia (21.91%), aplastic anemia (14.13%), chronic granulocytic leukemia (11.55%), idiopathic thrombocytopenic anemia (9.29%), malignant lymphoma (9.13%) and iron deficiency anemia (7.11%) . Total mortality was 18.73%. The importand cause of death were hemorrhage (37.3%), anemia (31.1%) and infection (25.2%).

本文报导了我院1960~1986年血液病的住院病例3,263例,占内科住院病例的5.73%。共有23种血液病。其中急白21.91%,再障14.13%,慢粒白11.55%,ITP9.29%,淋巴瘤9.13%和缺铁性贫血7.11%。死亡病例611例(18.73%)。死亡原因中出血37.3%,贫血31.1%和感染25.2%为多见。

Megakaryocytes of hematological diseases were retrospectively reviewed in ourcore biopsies.The diseases included various types of leukemia,myelofibrosis,chronic aplastic anemia,myelodysplastic syndromes,paroxysmal nocturnal hemoglobinuria,multiple myeloma,lymphoma of bone marrow,hemolytic anemia,primary thrombo-cytosis,idiopathic thrombocytopenic purpura,polycythemia vera,etc.It was verifiedthat in normal bone marrow,the megakaryocytes were distributed sparsely,but theymight gather in groups in hyperplastic...

Megakaryocytes of hematological diseases were retrospectively reviewed in ourcore biopsies.The diseases included various types of leukemia,myelofibrosis,chronic aplastic anemia,myelodysplastic syndromes,paroxysmal nocturnal hemoglobinuria,multiple myeloma,lymphoma of bone marrow,hemolytic anemia,primary thrombo-cytosis,idiopathic thrombocytopenic purpura,polycythemia vera,etc.It was verifiedthat in normal bone marrow,the megakaryocytes were distributed sparsely,but theymight gather in groups in hyperplastic conditions.The megakaryoblasts and immaturemegakaryocytes tended to gather intimately along trabeculae of the bone marrow,the number of megakaryocytes was significantly decreased in aplastic anemia ordecreased in certain degrees in pure erythrocytic anemia,ALL,CLL,PNH,multiple myeloma,or in rare cases of ITP.The cells were increased in numberin primary thrombocytosis,ITP,MF and CML.The structural anormaly involvedmicro-megakaryocytes,large megakaryocytes with mononuclei,bi-,tri-or poly-nuclei megakaryocytes,megakaryocytes with many nuclei arranged in ring-forms,megakaryocytes,with other cells in the demarcation systems,degenerated megakary-ocytes,naked megakaryocytes and megakaryocytic cytoplasma without nuclei.Thesignificance of these abnormal appearances in blood disease was discussed.

本文通过对本院历年来各种血液病骨髓活检的组织学观察,将所见的各种正常和异常的巨核细胞的数量、分布及形态学的变化作了描述,并对各种异常巨核细胞在血液病中的意义进行了讨论。巨核细胞是骨髓中体积最大,形态比较特殊而变化多样的细胞,它和其它骨髓造血细胞不同的是,随着细胞的发育成熟,倍体数增加,胞体逐渐由小变大,最大可达正常细胞的数十倍。在一些疾病因较其它造血细胞对致病因素更敏感,巨核细胞的数量常可发生很大改变。正常成熟的巨核细胞容易辨认,但幼稚或异常巨核细胞则容易被误认为其它造血或非造血细胞,为此我们对本院历年来的骨髓活检标本650例(次)中所见的正常及异常巨核细胞作一描述。

 
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