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
   skeletal deformity 的翻译结果: 查询用时:0.196秒
图标索引 在分类学科中查询
所有学科
畜牧与动物医学
口腔科学
儿科学
更多类别查询

图标索引 历史查询
 

skeletal deformity
相关语句
  骨骼畸形
     Subarticular bone absorption 7 cases(50.0%),Skeletal deformity 5 cases(41.6%);
     软骨下骨吸收7例(50.0%); 骨骼畸形5例(41.6%);
短句来源
     Fetal death rates in rats were 10.2%, 17.4%, 24.8% and 61.1%, proportions of skeletal deformity were 1 89%, 3.12%, 17.28% and 78.57%, and embryo deformity rates were 3.16%, 5.32%, 13.79% and 40.48% 48 hours after exposure, respectively for those exposed to various doses of arsenic.
     胎鼠死亡率分别为10.2%,17.4%,24.8%和61.1%; 骨骼畸形率为1.89%,3.12%,17.28%和78.57%;
短句来源
     The threshold of teratogenic effect of AN through subcutaneous injection was 15 mg/kg body weight,and the teratogenic index was 6\^3.The major malformation was skeletal deformity,and the major external malformations were tail deletion and short tail.
     本实验皮下注射AN染毒的致畸最低剂量为 15mg·kg-1,致畸指数为 6 3,以骨骼畸形为主 ,外观畸形主要为无尾、短尾等。
短句来源
     Bronchial obliteration was seen bronchoscopically in one case, while skeletal deformity and cardiovascular malformation were found in 9 and 2 cases, respectively.
     支气管镜检示支气管闭塞 1例 ,伴发骨骼畸形 9例 ,心血管畸形 2例。
短句来源
  “skeletal deformity”译为未确定词的双语例句
     To study the state of bone metabolism in children with skeletal deformity .
     【目的】 研究有骨骼畸形的小儿体内骨代谢状况。
短句来源
  相似匹配句对
     To study the state of bone metabolism in children with skeletal deformity .
     【目的】 研究有骨骼畸形的小儿体内骨代谢状况。
短句来源
     Madelung Deformity
     Madelung氏畸形
短句来源
     Severity of dentofacial deformity, the motivations and the outcome of surgery in skeletal Class Ⅲ patients
     Ⅲ类错畸形的骨骼畸形程度与治疗动机和治疗结果(英文)
短句来源
     Hemangioma of skeletal mucle
     四肢肌肉血管瘤
短句来源
     Skeletal Deformities in Poultry
     禽的骨骼畸形
短句来源
查询“skeletal deformity”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。
  skeletal deformity
We emphasize that parathyroidectomy should be performed in patients with our criteria, before progression of vascular calcification and skeletal deformity.
      
However, the timing of this operation was important, because skeletal deformity and vessel calcification did not improve after parathyroidectomy.
      
In our experience, parathyroidectomy is an effective treatment; however, the timing of the operation is important, because skeletal deformity and vessel calcification cannot be expected to diminish even after successful surgery.
      
The type IA osteogenesis imperfecta (OI) phenotype is characterized by multiple fractures, blue sclerae, and minimal skeletal deformity without dentinogenesis imperfecta.
      
Neurologic function, cerebrospinal fluid (CSF) circulation, skeletal deformity and the urinary transport system need to be kept in mind and need to be treated with cooperation between the different specialties.
      
更多          


This is a preliminary report of X-ray diagnosis on osteopetrosis ga-llinarum. Twenty natural cases of the disease were discovered and studied by X-ray examination.Avian skeleton radiography is a useful and practicable aid to the diagnosis of osteopetrosis and is a more reliable method than others to detect lesions of the bones in live chickens.Radiographic signs of the disease are increase in density of bilateral bones, osteosclerosis with thickening of the cortex and stricture or obliteration of the medullary...

This is a preliminary report of X-ray diagnosis on osteopetrosis ga-llinarum. Twenty natural cases of the disease were discovered and studied by X-ray examination.Avian skeleton radiography is a useful and practicable aid to the diagnosis of osteopetrosis and is a more reliable method than others to detect lesions of the bones in live chickens.Radiographic signs of the disease are increase in density of bilateral bones, osteosclerosis with thickening of the cortex and stricture or obliteration of the medullary cavity. Pathologic changes of the skeleton were observed in most bones of the body, but they were most frequently encountered in the long bones of the extremities. The pathologic process affected the tibia first and its incidence was the highest (20/20), while the figures of other bones were, for the femur 12/20, the coracoid 11/20, the ulna 11/20 and the radius 11/20. The lowest incidences were encountered in the metatarsus 6/20 and phalanges 3/20. X-ray presentation of the disease might be divided into the following types. ( a ) fusiform deformity and sclerosis of the long bones in the extremities, especially in the metatarsus; (b)deformity of the long bones of the pelvic extremities with diffuse osteosclerosis; ( c ) difuse osteosclerosis without skeletal deformity; (d) partly proliferation and sclerosis in the endosteum or small focal osteosclerosis, which were ordinarily well-defined in the tibia and were sometimes found in the femur or ulna. The first type of X-ray presentation might only be in young chickens, while other types might generally occur in adult chickens without "bootlike" deformity of the metatarsus.Differential diagnosis of other avian osteopathies, for example, rickets, osteoporosis, periostosis, staphylococcosis, chronic osteomyelitis, osteosarcoma and Paget's disease was discussed. Radiopraphy of a shank is recommended as a means to detect this disease in general survey.

1、本文在国内首次报告了鸡骨质石化病的X线诊断,利用X线检查,共发现了20只本病的自然病鸡。鸡的骨骼X线照相对诊断骨质石化病是有效可行的。在生前检出骨骼的病变较其他方法更为可靠。 2、本病的X线征为双侧骨骼的密度增高和骨质硬化,骨皮质变厚,骨髓腔变窄甚至闭塞。病变可见于多骨,但最常发生在四肢长骨。最先损害的是胫骨,其发生率最高(20/20);股骨其次(12/20);而乌喙骨、尺骨和桡骨再其次,均为11/20;跖骨较低(6/20);趾骨最低,只有3/20发生病变。其X线表现可分为四种类型:(1)四肢长骨(尤其跖骨)梭状畸形与骨质硬化;(2)后肢长骨畸形与泛发性骨质硬化;(3)泛发性骨质硬化但无骨骼畸形;(4)胫骨骨内膜局限性增生硬化或小灶性硬化,有时累及股骨或尺骨。第一种类型的表现可能只发生于仔鸡。没有跖骨“靴样”畸形的其他类型通常见于成年鸡。 3、对其他骨病如佝偻病、骨质疏松、骨膜骨质增生、葡萄球菌病、慢性骨髓炎、成骨肉瘤和佩吉特氏病(Paget’s disease)等的区别诊断作了讨论,并建议在大群检疫时用一侧胫骨的X线照相作为检出该病的方法。

Five cases of Holt-Oram Syndrome were reported.Two of them were consideredto be sporadic mutation.All patients had various degrees of skeletal defects.Therewas striking asymmetry of skeletal involvement,with the left side more severelyaffected.The most frequently involved structures were the thumbs(5 cases)andfirst metacarpal(5 cases),less frequently were the carpal bones,while arm bonesincluding the shoulder girdle were somewhat involved in various degrees.3 patients had well-defined cardiac abnormalities,2...

Five cases of Holt-Oram Syndrome were reported.Two of them were consideredto be sporadic mutation.All patients had various degrees of skeletal defects.Therewas striking asymmetry of skeletal involvement,with the left side more severelyaffected.The most frequently involved structures were the thumbs(5 cases)andfirst metacarpal(5 cases),less frequently were the carpal bones,while arm bonesincluding the shoulder girdle were somewhat involved in various degrees.3 patients had well-defined cardiac abnormalities,2 cases had congenital heartdisease,(1 VSD+left vena cava superior,1 ASD),1 case had cardiomegalywith undefined lesion.ECG was available in 2 cases with rhythm disturbance.CHD is not a constant feature of HOS,but family members of HOS patients withspecial skeletal defects alone must be considered as having HOS,since they canhave offsprings affected with both CHD+skeletal defects.Case 1 and 2 were theexample.There was no correlation between the severity of skeletal deformity and thepresence of cardiac disease.Consideration of HOS is important in the evaluation of patients with CHD.A searchfor associated skeletal defect is justified and often appropriate genetic counsellingfor both the patient and parents.

从五例家族性先心病台并上肢骨发育畸形患者的 X 线检查,征实拇指及第一掌骨缺如或发育不全,其他骨亦可有类似改变。病变常不对称,左侧显著。心电图常有节律障碍。多数患者有先心病——房缺或室缺。先心痛和骨缺损二者的严重程度似无明确关系。

A new broad-spectrum anthelmintic agent tribendimidin wasstudied for its mutagenicity and teratogenicity.No mutagenic effect was obser-ved by the following three tests:Salmonella/microsome system with TA 97,TA 98,TA100 and TA 102;micronucleus test in NIH mice administered up to500 mg/kg(about 1/2 LD50);in vitro chromosomal aberration test with Chinesehamster lung fibroblast cell line.No evidence of external and internal malfor-mations and skeletal deformities were observed in pregnant rats administeredorally...

A new broad-spectrum anthelmintic agent tribendimidin wasstudied for its mutagenicity and teratogenicity.No mutagenic effect was obser-ved by the following three tests:Salmonella/microsome system with TA 97,TA 98,TA100 and TA 102;micronucleus test in NIH mice administered up to500 mg/kg(about 1/2 LD50);in vitro chromosomal aberration test with Chinesehamster lung fibroblast cell line.No evidence of external and internal malfor-mations and skeletal deformities were observed in pregnant rats administeredorally up to daily dose of 200 mg/kg from d8 to d10 of gestation.

驱钩新化合物王苯双脒(Tribendimidin)用鼠伤寒沙门氏菌/微粒体酶系统检测,对 TA 97,TA98,TA 100及 TA 102菌株未见诱变性。小鼠 ig 500 mg/kg 后24 h 的骨髓微核试验结果为阴性,未见染色体畸变。培养的中国仓鼠肺成纤维细胞系的染色体畸变试验也为阴性。孕大鼠于 d 8~d 10每日 ig 200 mg/kg,未见有胚胎毒性及致畸性。

 
<< 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skeletal deformity的内容
在知识搜索中查有关skeletal deformity的内容
在数字搜索中查有关skeletal deformity的内容
在概念知识元中查有关skeletal deformity的内容
在学术趋势中查有关skeletal deformity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