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心脏畸形     
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  cardiac anomalies
     One-stage correction of aortic arch obstruction associated with cardiac anomalies in 18 cases
     主动脉弓阻塞合并心脏畸形18例的一期矫治
短句来源
     Ninety-two cases of ventricular septal defects associated with various cardiac anomalies were reported.
     本文报告室间隔缺损合并其他心脏畸形92例,占同期行室间隔缺损修补术病例13%。
短句来源
     The phenotypes of the genital malformation and the dislocation of hip joint are associated with the duplication of 7p15.The cardiac anomalies is resulted from the dysfunctions of several genes on the long arm of chromosome 7.The gene associated with the craniosynostosis may locate on the region of 7p21.2→p21.3.
     结果表明 ,7p2 1 .2→p2 2是 7p部分三体综合征的关键片段 ,生殖器畸形、髋关节脱位与 7p1 5重复有关 ,心脏畸形与 7p多个基因作用有关 ,颅缝早闭基因可能位于 7p2 1 .2→p2 1 .3。
短句来源
     In one patient there was pure DCRV, and the remaining 51 patients DCRV was associated with other congenital cardiac anomalies, in which VSD was the most common (50), followed in order by pulmonary stenosis (6), aortic valve prolapse (4), atrial septal defect (2), and subaortic stenosis (1).
     单纯性DCRV 1例,合并其它先天性心脏畸形51例,以室间隔缺损(VSD)最多见(50例),其次是肺动脉瓣狭窄(6例)、主动脉瓣脱垂(4例)、房间隔缺损(2例)和主动脉瓣下狭窄等。
短句来源
     Conclusion One-stage complete correction of IAA and COA with cardiac anomalies through median sternotomy yields excellent intermediate surgical results.
     结论正中开胸一期矫治COA及IAA合并心脏畸形可获得满意的近期疗效。
短句来源
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  cardiac anomaly
     Analysis of differential expression gene between monozygotical twins with cardiac anomaly
     同卵双胎心脏畸形差异表达基因的分析
短句来源
  cardiac malformation
     It can get good result to resect diaphragm of left atrium and correct associated cardiac malformation simultaneously.
     三房心是一种罕见的心脏畸形,多合并其他心内畸形,手术切除左房内隔膜并同时矫治其他心内畸形可获得满意的效果。
短句来源
     Ebstein anomaly is an uncommon congenital cardiac malformation. From Nov.1989 to July. 1993,5 patients with Ebstein anomaly were treated surgically.
     我所自1989年11月至1993年7月为5例Ebstein心脏畸形病人施行了外科治疗。
短句来源
     Clinical significance and effect in the antenatal diagnosis of fetal congenital cardiac malformation using the four-chamber view
     四腔心切面在产前超声诊断先天性心脏畸形中的作用
短句来源
     A clinical analysis of 17 congenital bicuspid aortic valve (OBAV) cases discovered 29.4% OBAV with other cardiac malformation. OBAV may be a common complex congenital cardiac malformation.
     本文通过对17例先天性二叶式主动脉瓣(CBAV)病例的临床分析,发现29.4%的CBAV合并其他心脏畸形,可能是一种常见的复杂性先天性心脏畸形
短句来源
     Objective:To evaluate the clinical significance and effect of the anomalies seen at the four-chamber view antenatally in diagnosis of fetal congenital cardiac malformation.
     目的:分析四腔心切面所见异常在产前超声诊断先天性心脏畸形中的作用和临床意义。
短句来源
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  cardiac defects
     Based on Richardson's classification,type I in 7 cases,type II in 3,and type III in 5. Eight cases were associated with other cardiac defects (53.5%),including 4 cases with complicated cardiac defects (26.7%).
     按Richardson分型 ,I型 7例 ,II型 3例 ,III型 5例。 8例合并其他心脏畸形 ,其中 4例合并复杂畸形 (2 6 7% )。
短句来源
     Methods: A total of 45 children accepted correction of cardiac defects were allocated into three groups(group Ⅰ:no myocardial ischemia, group Ⅱ:myocardial ischemia less than 60 min, and group Ⅲ:myocardial ischemia more than 60 min). Blood samples were collected before skin incision and at 1 h, 6 h, 12 h,24 h,48 h, 72 h,96 h after operation or reperfusion. The levels of CK GA MB, LDH and h-FABP were determined.
     方法:将45例先天性心脏畸形矫治术患儿分为3组,每组15例,Ⅰ组为心肌未缺血组,Ⅱ组为心肌缺血时间小于60min组,Ⅲ组为心肌缺血时间大于60min组,分别于切皮前、开放循环后(Ⅰ组为手术结束后)1h,6h,12h,24h,48h,72h,96h取静脉血,检测血清hFABP、LDH和CKMB浓度。
短句来源
     By statistical analysis of 47 cases with Holt Qram syndrome(HOS), we found that the severity of the upper limb abnormalities and cardiac defects in HOS varied significantly with different individuals.
     通过对 47例心手综合征 (Holt Oramsyndrome ,HOS)病人上肢畸形和心脏缺损进行统计分析 ,发现心手综合征病人上肢畸形与心脏畸形均有很大的个体差异。
短句来源
     Methods: From June, 1999 to May, 2000, 45 children (30 male, 15 female) undergoing correction of cardiac defects were divided into three groups randomly: group I no myocardial ischemia, group II myocardial ischemia less than 60 minutes, group III myocardial ischemia >60 minutes.
     方法  1999年 6月至 2 0 0 0年 5月 ,45例先天性心脏畸形矫治术病儿中 ,男 30例 ,女15例。 随机分为 3组 ,每组 15例 ,I组为心肌未缺血组 ;
短句来源
     Methods: From June 1999 to March 2000, 40 children undergoing correction of cardiac defects were divided into two groups randomly: group A modified St. Thomas No1 solution, and group B using same solution but enriched with 10 mmol/L exogenous creatine phosphate.
     方法  1999年6月至 2 0 0 0年 3月 ,4 0例先天性心脏畸形矫治术 (男、女各 2 0例 )病儿随机分为两组 :冷高钾停搏液组及10mmol/L外源磷酸肌酸强化的冷高钾停搏液组。
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  cardiac anomalies
Preexisting venous channels as the persistent left superior vena cava are common in cardiac anomalies and may lead to postoperative deterioration and cyanosis.
      
There also is evidence that disturbances of autonomic function or certain structural cardiac anomalies may be more common in cluster headache sufferers.
      
Patients with VCFS have cardiac anomalies, cleft palate, learning problems, and speech and developmental delays.
      
Correction of corrected transposition of the great arteries associated with cardiac anomalies
      
Total cavopulmonary connection for complex cardiac anomalies with the functional single ventricle
      
更多          
  cardiac anomaly
Acute heart failure may be due to a congenital structural cardiac anomaly in spite of the age of 54.
      
Patients with Sano shunts tend to be more stable thus reducing the interstage mortality of this still challenging complex cardiac anomaly.
      
Congenitally corrected transposition of the great vessels is a cardiac anomaly in which the pulmonary artery and the aorta are transposed in relation to one another but in which the flow of blood is maintained in the physiologic direction.
      
Although each of these complications is rare in and of itself, this case demonstrates the entire spectrum of complications from a single uncorrected congenital cardiac anomaly.
      
Unilateral absence of a pulmonary artery is an uncommon condition and usually complicated by a cardiac anomaly.
      
更多          
  cardiac malformation
Aortico-left ventricular tunnel (ALVT) is a rare congenital cardiac malformation that presents with cardiac failure and clinical findings of severe aortic regurgitation in early infancy.
      
Therefore, knowledge of this rare cardiac malformation is mandatory if an infant presents with findings of aortic regurgitation.
      
Our case shows that complete echocardiographic evaluation is possible in infants with this complex cardiac malformation.
      
Tetralogy of Fallot is the most common cyanotic cardiac malformation in late childhood and adult, occurring in approximately 0.25 of 1000 live births.
      
Congenitally corrected transposition of the great arteries is a relatively rare cardiac malformation characterized by atrioventricular and ventriculoarterial discordance.
      
更多          
  cardiac defects
Up to 45% of the patients may have associated cardiac defects, and the development of this bizarre lesion is still unclear.
      
The hypoxia-inducible factor HIF-1 promotes intramyocardial expression of VEGF in infants with congenital cardiac defects
      
The hypoxia-inducible factor HIF-1 promotes intramyocardial expression of VEGF in infants with congenital cardiac defects
      
Mutations in these genes can cause a variety of cardiac defects even within the same family.
      
DiGeorge syndrome is characterized by conotruncal cardiac defects, hypocalcemia, and a hypoplastic thymus.
      
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