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nephritic syndrome
相关语句
  肾病综合征
     The positive rate was 67.1%in group A,26.6% in group B and 6% in patients with nephritic syndrome.
     A组的C1qAb阳性率为67.1%,而B组阳性率仅为26.6%; 肾病综合征组阳性率为6%。
短句来源
     The most common clinical syndrome was chronic nephritic syndrome(CNS)((43.8)%),followed by nephrotic syndrome(NS)((42.2)%).
     最常见的临床综合征是慢性肾炎综合征(CNS)(43.8%)和肾病综合征(NS)(42.2%)。
短句来源
     Results Nephrotic syndrome was the most common clinical manifestation(30.9%),followed by simple hematuria(25.5%),hematuria with proteinuria(23.6%),acute nephritic syndrome((18.2%)) and chronic nephritic syndrome(1.8%).
     结果临床表现为肾病综合征占30.9%、孤立性血尿占25.5%、血尿蛋白尿占23.6%、急性肾炎综合征占18.2%、慢性肾炎综合征占1.8%;
短句来源
     Transforming growth factor-beta 1(TGFβ_1) and its clinical significances in patients with nephritic syndrome
     肾病综合征患者尿TGFβ_1检测的临床意义
短句来源
     The Resistance of Insulin and the Expression of ISNR-β,CPR,eNOS in Renal Tissue in Primary Nephritic Syndrome
     原发性肾病综合征患者胰岛素抵抗及肾组织ISNR-β、CPR、eNOS的表达
短句来源
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  肾炎综合征
     The most common clinical syndrome was chronic nephritic syndrome(CNS)((43.8)%),followed by nephrotic syndrome(NS)((42.2)%).
     最常见的临床综合征是慢性肾炎综合征(CNS)(43.8%)和肾病综合征(NS)(42.2%)。
短句来源
     Results Nephrotic syndrome was the most common clinical manifestation(30.9%),followed by simple hematuria(25.5%),hematuria with proteinuria(23.6%),acute nephritic syndrome((18.2%)) and chronic nephritic syndrome(1.8%).
     结果临床表现为肾病综合征占30.9%、孤立性血尿占25.5%、血尿蛋白尿占23.6%、急性肾炎综合征占18.2%、慢性肾炎综合征占1.8%;
短句来源
     Renal lesions included asymptomatic hematuria and/or proteinuria (71.0%), acute nephritic syndrome (6.5%), nephrotic syndrome (2.6% ), rapid progressive glomerulonephritis (1.3% ), renal embolism (1.3% ), isolated pyuria(3.2%), renal lesion not directly related to IE(2.6%).
     肾损害表现包括无症状血尿和(或)蛋白尿(71.0%)、急性肾炎综合征(6.5%)、肾病综合征(2.6%)、急进性肾炎综合征(1.3%)、肾栓塞(1.3%)、单纯白细胞尿(3.2%)、非IE直接所致肾损害(2.6%)。
短句来源
     ④IgA nephropathy increased significantly (from 16.9% to 47%),which accounted for 15% patients with massive proteinuria,49.6% patients with nephritic syndrome,42.3% patients with isolated hematuria.
     (4 )在原发性肾小球疾病中 ,IgA肾病所占比例明显增多 (16.9%至 47% ) ,占大量蛋白尿患者的 15 % ,肾炎综合征的 49.6% ,单纯血尿的 42 .3 %。
短句来源
     Clinical features included proteinuria and/or hematuria (34.0%),nephrotic syndrome (47.3%),acute renal failure (10.7%),and acute nephritic syndrome (8.0%).
     临床表现蛋白 尿和(或)血尿占34.0%,肾病综合征占47.3%,急性肾衰竭占10.7%,急性肾炎综合征占8.0%。
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  肾病综合症
     Inquiry On Relation Between T lymphocyte Subgroup and Immunoglobulin IgG,IgA with Nephritic Syndrome
     T淋巴细胞亚群和IgG、IgA变化与肾病综合症关系的探讨
短句来源
     Conclusion: TT genotype of M235T angiotensinogen gene may be associated with the pathogenesis of nephritic syndrome in children.
     结论:血管紧张素M2 35T基因TT型可能与小儿肾病综合症的发病密切相关;
短句来源
     2.transfer 278 case histories with acute glomerulonephritis, nephritic syndrome and urinary tract infections and analyze them statistically.
     2、抽取1989年—1991年和1999年—2001年间的急性肾炎、肾病综合症、泌尿道感染、紫癜性肾炎病人的病案,记录其发病季节、诱因、年龄、性别、族别等进行详细统计分析。
短句来源
     Study on gene polymorphism of renin angiotensin system in children with nephritic syndrome
     小儿肾病综合症肾素-血管紧张素系统基因多态性研究
短句来源
     (3)The conductivity levels in urine samples from acute glomerulonephritis,chronic glomerulonephritis,nephritic syndrome,renal calculus,calculus of ureter,diabetes,hypertension patients are lower than from healthy controls.
     (3)急性肾小球肾炎、慢性肾小球肾炎、肾病综合症、肾结石、输尿管结石、糖尿病、高血压等病人的尿电导率均偏低。
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  “nephritic syndrome”译为未确定词的双语例句
     ③The frequency of the gene polymorphisms of the angiotensin-converting enzyme (ACE) gene: In the nephritic syndrome group, the frequency of Ⅱ, DI, DD genotype were 45.0%, 42.5%, 12.5% respectively, and in the control group, the frequency of Ⅱ, DI, DD genotype were 46.0%, 44.0%, 10.0% respectively; there was no statistic difference between the two groups (P>0.05);
     ③血管紧张素转换酶基因多态性Ⅱ、DI、DD基因型肾病组分别为4 5 0 %、4 2 5 %、12 5 % ,对照组分别为4 6 0 %、4 4 0 %、10 0 % ,差异无显著性(P >0 0 5 )。
短句来源
     IgG,IgM,IgE had significant difference between nephritic syndrome children and healthy children(Pa<0.05).
     NS与正常对照组比较,IgG、IgM、IgE具有显著性差异(Pa<0.05);
短句来源
     ②The frequency of the gene polymorphisms of angiotensin Ⅱ receptor type Ⅰ gene: In the nephritic syndrome group, the frequency of AA, AC, CC genotype were 45.0%, 27.5%, 27.5% respectively. In the control group, the frequency of AA, AC, CC genotype were 68.0%, 20.0%, 12.0% respectively; there was no statistic difference between the two groups (P>0.05).
     ②血管紧张素Ⅱ受体Ⅰ基因多态性AA、AC、CC基因型肾病组分别为4 5 0 %、2 7 5 %、2 7 5 % ,对照组分别为6 8 0 %、2 0 0 %、12 0 % ,差异无显著性(P >0 0 5 )。
短句来源
     Results: ①The frequency of the gene polymorphisms of M235T angiotensinogen gene: In the nephritic syndrome group, the frequency of MM, MT, TT genotype were 37.5%, 27.5%, 35.0% respectively, and in the control group, the frequency of MM? MT?
     结果:①血管紧张素M2 35T基因多态性MM、MT、TT基因型肾病组分别为37 5 %、2 7 5 %、35 0 % ;
短句来源
     which were striking higher than in control group(21.92% and 75.00% respectively, P<0.05) Conclusion: nephritic syndrome No.
     结果:治疗组完全缓解率和总有效率分别为33.37%和94.00%,显著高于对照组的21.92%和75.00%。
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  nephritic syndrome
Because laboratory findings revealed massive proteinuria and hypoproteinemia, he was diagnosed as having nephritic syndrome caused by minimal change disease.
      
Six months after the onset of the acute nephritic syndrome, the patient remained asymptomatic, except for microhematuria.
      
After 2 weeks of observation, blood pressure, C3 level, and ASO titer had returned to normal, although the persisting nephritic syndrome necessitated steroid therapy.
      
Nineteen years later, acute nephritic syndrome with hypocomplementemia and an increasing anti-streptolysin O (ASO) titer developed 2 weeks after the onset of an upper respiratory infection.
      
Glomerulointerstitial events in rapidly progressive nephritic syndrome, with special reference to histologic grade and stage on
      
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The clinical features of 8 cases of lupus glomerulonephritis were analyzed. Among them, 7 were females and one male. Their ages ranged from 8 to 12 years. In all but one case, the evidence of nephritic damage appeared about one month after the onset of lupus erythematosus. It is believed at the present time that pathological changes may be altered after treatment or with the changes in clinical conditions. 2 cases showing glomerulonephritis at the onset of the disease eventually developed nephritic syndrome....

The clinical features of 8 cases of lupus glomerulonephritis were analyzed. Among them, 7 were females and one male. Their ages ranged from 8 to 12 years. In all but one case, the evidence of nephritic damage appeared about one month after the onset of lupus erythematosus. It is believed at the present time that pathological changes may be altered after treatment or with the changes in clinical conditions. 2 cases showing glomerulonephritis at the onset of the disease eventually developed nephritic syndrome. Repeated searches for LE cells would be of help in diagnosis. Beneficial effects were obtained in 4 cases who received prednisone and cyclophosphamide or azathioprine combined therapy, 3 of them had remission for one to two and half yeats.

本文报道儿童狼疮性肾炎(SEEK)8例,以女性学龄儿童发病为主。除1例外,其余均于红斑性狼疮起病1个月左右出现肾损害症状。8例中,有2例起病时为肾炎后转归为肾病综合征。多次检查狼疮细胞有助于诊断。4例用类固醇与免疫抑制剂治疗,3例获得1~2 1/2年缓解。

180 cases of anaphylactoid purpura nephritis with various clinical patterns wer analysed. 51.1% of the cases showed proteinuria and/or hematuria only, 43.3% manifested as nephritic syndrome, and 5.6% as nephrotic syndrome with hematuria. There were no clinical correlations between the renal and extrarenal symptoms. The outcome of patients with steroid therapy was not significantly different from those without steroid treatment. 40.6% of the patients were cured,42.2% improved, 16.1% unchanged and...

180 cases of anaphylactoid purpura nephritis with various clinical patterns wer analysed. 51.1% of the cases showed proteinuria and/or hematuria only, 43.3% manifested as nephritic syndrome, and 5.6% as nephrotic syndrome with hematuria. There were no clinical correlations between the renal and extrarenal symptoms. The outcome of patients with steroid therapy was not significantly different from those without steroid treatment. 40.6% of the patients were cured,42.2% improved, 16.1% unchanged and 1.1% died at discharge from the hospital.76 cases were followed up for 11 months to 26 years (mean 9 years). All of them were physically normal. Detail studies had been carried out in 50 cases. 30% were cured. 24% still showed some abnormal urine findings and 46% showed abnormal urine with mild azotemia. Renal biopsy was done in 7 cases with abnormal findings. Biopsy samples were examimed with light microscopy, electron microscopy and im-munoflorescence. 5 cases were diagnosed .as mesangial proliferative glomerulonephritis, and the other 2 as membrano-proliferative glomerulonephritis. No crescent formation was found. IgA deposits in the glomeruli were seen in 5 of the 6 cases examimed. Tne outcome of this series was better than other reports.

本文对儿科医院1956年9月至1983年8月住院的过敏性紫癜肾炎(APN)180例作了临床分析,其临床表现为血尿和/或蛋白尿者占51.1%、肾炎综合征者占43.3%、肾病综合征伴血尿者占5.6%。肾损害与肾外症状无明显关系,用激素治疗与否对近期结局无明显影响,近期临床痊愈40.6%、好转42.2%、无变化16.1%、死亡1.1%。 76例随访11月至26年(平均9年),体检无异常发现。在资料完整的50例中痊愈30%、尿异常24%、尿异常伴轻度氮质血症46%。作肾活检7例,其血清C_3均正常,经光镜、电镜、免疫荧光检查2例呈膜增殖肾炎、5例呈系膜增殖肾炎,未见新月体形成,有IgA沉积者5/6例。本组APN的预后较其它文献报告佳。

The peripheral blood T lymphocyte subsets and ConA-induced suppressor cell activity (ConA-SCA) were determined in 37 patients with primary nephritic syndrome(PNS). The results showed that the patients in initial onset had the abnormal number and function of T lymphocytes, which returned to a normal level with treatment with steroid and improvement of patients'condition. The indings suggest that the immunoregulatory imbalance of this disease may be a primary change and play an important role in pathogenesis...

The peripheral blood T lymphocyte subsets and ConA-induced suppressor cell activity (ConA-SCA) were determined in 37 patients with primary nephritic syndrome(PNS). The results showed that the patients in initial onset had the abnormal number and function of T lymphocytes, which returned to a normal level with treatment with steroid and improvement of patients'condition. The indings suggest that the immunoregulatory imbalance of this disease may be a primary change and play an important role in pathogenesis of PNS.

本文检测了37例原发性肾病综合征患儿的外周血T淋巴细胞亚群和刀豆素A诱导的抑制细胞活性水平。结果显示,肾病患儿初发时就存在抑制性T细胞数量及功能的减低,并随着激素治疗及病情的好转而恢复正常,提示本病的免疫调节失衡可能是一原发性改变,在肾病发病机理中起一定的作用。

 
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