助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   bone 在 心血管系统疾病 分类中 的翻译结果: 查询用时:0.176秒
图标索引 在分类学科中查询
所有学科
心血管系统疾病
外科学
生物医学工程
口腔科学
内分泌腺及全身性疾病
中药学
特种医学
预防医学与卫生学
肿瘤学
更多类别查询

图标索引 历史查询
 

bone
相关语句
  骨髓
    A study on T cell clones from bone marrow of an aplastic anemia patient
    再生障碍性贫血骨髓T淋巴细胞克隆的研究
短句来源
    Studies on Migration and Its Mechanism in Bone Marrow Mesenchymal Stem Cell Transplantation for Myocardial Infarction in Rats
    大鼠骨髓间充质干细胞移植修复梗死心肌过程中的迁移现象及机制研究
短句来源
    The Experimental Study of Bone Marrow Mononuclear Cell Transplantation on Infarcted Cardiac Function
    骨髓单个核细胞移植对心肌梗死后心功能影响的实验研究
短句来源
    Therapeutic Effects of Bone Marrow Stem Cells Mobilization with G-CSF on Acute Myocardial Infarction in Rats
    G-CSF动员骨髓干细胞治疗大鼠急性心肌梗死的疗效观察
短句来源
    Preliminary Study on Biological Properties of Bone Marrow Mesenchymal Stem Cells and Therapeutic Effection on Myocardial Ischemia
    骨髓间质干细胞的生物学特性及对心肌缺血治疗作用的初步研究
短句来源
更多       
  “bone”译为未确定词的双语例句
    IgD MULTIPLE MYELOMA (WITH 2 CASES SHOWING DIFFUSE SCLEROTIC BONE LESIONS)
    IgD型骨髓瘤(2例伴弥漫性骨质硬化)
短句来源
    LARGE VOLUME CRYOPRESERVATION OF HUMAN BONE MARROW AND CLINICAL APPLICATION
    大容积人骨髓的低温保存及临床应用
短句来源
    Clinical and Pathologic Analysis of Bone Marrow Fibrosis—Discussion on classification
    骨髓纤维化临床与病理分析—关于分型问题的讨论
短句来源
    Study on hemopoietic strcmal stem cells I .Hemopoietic reconstitution cf bone marrow in situ
    造血基质干细胞的研究Ⅰ.原位骨髓的造血重建
短句来源
    Study on hemopoietic stromal stem cells II. Kemcpcietic reconstitution of bone marrow of ectopically implanted bone
    造血基质干细胞的研究Ⅱ.异位移植骨髓的造血重建
短句来源
更多       
查询“bone”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  bone
Biomimetic strengthening polylactide scaffold materials for bone tissue engineering
      
The novel composite mainly consists of nano-hydroxyapatite (n-HA), which is the main inorganic content in natural bone tissue for the PLA.
      
The crystal degree of the n-HA in the composite is low and the crystal size is very small, which is similar to that of natural bone.
      
The biomimetic three-dimensional porous composite can serve as a kind of excellent scaffold material for bone tissue engineering because of its microstructure and properties.
      
The effects of hematopoietic stem/progenitor cells (HSPCs) expanded in the two step coculture with human bone marrow mesenchymal stem cells (hMSCs) on the hematopoietic reconstruction of irradiated NOD/SCID mice were studied.
      
更多          


Chromosome analysis of metaphases from bone marrow cells or cul-tured peripheral blood lymphocytes of 15 patients with blood disorderswas carried out. The final diagnoses of 12 patients were confirmed aschronic myeloid leukemia(CML). The clinical diagnoses of another 2 pa-tients were acute myeloid leukemia(AML), and the other 1 was secondarypolycythemia. Cytogenetically, the Ph~1 chromosomes were found among 11 of 12 pa-tients with CML, the mean of Ph~1 positive cells was 72.3%. The presenceof Ph~1 chromosomes...

Chromosome analysis of metaphases from bone marrow cells or cul-tured peripheral blood lymphocytes of 15 patients with blood disorderswas carried out. The final diagnoses of 12 patients were confirmed aschronic myeloid leukemia(CML). The clinical diagnoses of another 2 pa-tients were acute myeloid leukemia(AML), and the other 1 was secondarypolycythemia. Cytogenetically, the Ph~1 chromosomes were found among 11 of 12 pa-tients with CML, the mean of Ph~1 positive cells was 72.3%. The presenceof Ph~1 chromosomes in 2 cases with AML was emphasized and their diag-noses were discussed in detail. The percentage of Ph~1 positive cells in thecase of so called secondary polycythemia was 69.4%, the revised diagno-sis of this case was more likely to be polycythemia vera.

对15例血液病患者进行了骨髓或外周血培养细胞的染色体观察。15例中12例临床确诊为慢性粒细胞白血病,2例诊断为急性粒细胞白血病,1例为继发性红细胞增生症。在12例慢性粒细胞白血病中,11例Ph~1染色体为阳性(阳性率平均为72.3%),1例为Ph~1阴性;2例急性粒细胞白血病患者的骨髓中期分裂细胞具Ph~1染色体者分别占1/4及1/5,其中1例还发现微小体;1例继发性红细胞增生症患者,70%的骨髓中期分裂细胞为Ph~1染色体阳性,并发现染色体碎裂细胞。

This paper reports 5 cases of IgD multiple myeloma which is a very uncommon disease. In contrast to the other types of myeloma, these patients were younger in age, the oldest being 53 years of age, and 2 cases were below the age of 40. Their clinical manifestations appeared more severe ; extra-skeletal infiltrations were more common with hepatosplenomegaly in 3 cases and hepatomegaly in 1 case, the lymph nodes were enlarged in 1 case, biopsy of which showed infiltration of tumor cells. Anemia was present in...

This paper reports 5 cases of IgD multiple myeloma which is a very uncommon disease. In contrast to the other types of myeloma, these patients were younger in age, the oldest being 53 years of age, and 2 cases were below the age of 40. Their clinical manifestations appeared more severe ; extra-skeletal infiltrations were more common with hepatosplenomegaly in 3 cases and hepatomegaly in 1 case, the lymph nodes were enlarged in 1 case, biopsy of which showed infiltration of tumor cells. Anemia was present in 3 cases, the hemoglobin level in one case was only 3.5g %.Two cases had thrombocytopenia and purpura. Promyelocytes, myelocytes and nucleated red cells were seen in the peripheral blood smear in 2 cases. Bence-Jones protein was present in 4 cases, but the BUN was normal in all cases. Blood calcium was normal in 4 cases and the alkaline phosphatase level was increased in 3 cases. Serum analysis by cellulose acetate membrane electrophoresis showed the IgD M-protein to move between β and γ1 zones, with a slightly broader base and lower spike. Serum immunoelectrophoresis performed in 4 cases revealed heavy precipitin arcs against the anti-IgD serum. Semiquantitative determinations of IgD by the double immunodiffusion method showed the IgD content was not very high, in one of the cases it was only positive at 1 : 20, but the IgG, IgA and IgM were diminished in 4 cases, and were at the lower limit of normal values in 1 case.Two of the 5 cases were associated with diffuse sclerotic changes of the bones involving the spine, pelvis, ribs,clavicles and femurs which are considered extremely rare.

本文报道少见的IgD型多发性骨髓瘤5例。与其他类型的骨髓瘤比较,发病年龄轻,症状稍重,肝、脾、淋巴结多见有瘤细胞浸润,血清中IgD含量并不很高,而其它类型的Ig含量常减少。有骨质损害。其中有2例伴有更为罕见的弥漫性骨质硬化。

Pure red cell aplasia is a rare and special type of aplastic anemia. Bone marrow shows normal cellularity and normal white cell and platelet counts but there is a re-duced count in red series only. The primary and secondary forms of the disorder were noted, the former being immunologically orientated. Treatment with immunosuppressive agents often yielded satisfactory results. Six cases were observed in the Zhongshan Hospital since 1974. Four were male and two female. The ages ranged from 25 to 76 years....

Pure red cell aplasia is a rare and special type of aplastic anemia. Bone marrow shows normal cellularity and normal white cell and platelet counts but there is a re-duced count in red series only. The primary and secondary forms of the disorder were noted, the former being immunologically orientated. Treatment with immunosuppressive agents often yielded satisfactory results. Six cases were observed in the Zhongshan Hospital since 1974. Four were male and two female. The ages ranged from 25 to 76 years. No primary causes could be found, but one case had a tumor of undetermined nature in the thoracic cavity and another case had a history of contact with agricul-tural insecticides. The hematological findings revealed red cell count 1.02-1.95 million/mm~3, hemoglobin 3.S-7.5gm% and reticulocyte 0-0.5%, platelet and white cell counts were, normal. Bone marrow normoblast ranged from 0 to 3.5%. Immunoglobulin deter-mined in four cases showed normal value. The treatment differs from that of the aplastic anemia generally encountered. All six cases were treated with long-term mas-sive doses of androgen without any improvement. In three cases, corticostcroid was beneficial. In another case, after unsatisfactory treatment with corticosteroid, azathio-prine was used. The patient showed clinical improvement with his hemoglobulin main-tained above 9 gm%. The diagnosis and treatment of the disease were briefly discussed.

单纯性红细胞再障是一种罕见特殊类型的再障,血象及骨髓象中仅有红细胞减少而粒细胞及巨核细胞数正常.发病机制与免疫有关。本文报道自1964年来收治的6例。治疗用雄激素均无效,3例对皮质激素有效,1例经各种治疗无效后,用6硫唑嘌呤有效.本文对诊断及治疗进行了讨论.

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关bone的内容
在知识搜索中查有关bone的内容
在数字搜索中查有关bone的内容
在概念知识元中查有关bone的内容
在学术趋势中查有关bone的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社