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   prednisone treatment 的翻译结果: 查询用时:0.217秒
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prednisone treatment
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  强的松治疗
     The 81 ACA positive patients were treated orally with aspirin,25 ACA and ANA/ENA positive patients were treated with aspirin combined with prednisone,and 3 ANA/ENA positive patients with prednisone treatment oral.
     分别用阿斯匹林口服治疗81例ACA阳性病人 ,阿斯匹林 +强的松治疗 2 5例ACA和ANA/ENA阳性病人 ,强的松治疗 3例ANA/ENA阳性病人。
短句来源
     Methods One hundred and twenty two patients of idiopathic nephrotic syndrome with no IgA mesangial proliferative glomerulonephritis and sensitive to prednisone treatment were divided into two groups randomly.
     方法 将 12 2例呈肾病综合征表现并对强的松治疗敏感的非IgA系膜增生性肾炎患者随机分为两组 ,对照组按常规方法使用并撤减强的松 ,观察组在强的松常规治疗的基础上加用中药治疗。
短句来源
     After prednisone treatment,the blood plasma level of IL 13 was observed a significant decrease in steroid sensitive asthma ( P <0.05),and was not associated with significant changes in steroid resistant asthma ( P >0.05).
     激素抵抗或依赖型哮喘经强的松治疗 1周前后血浆IL 13质量浓度比较 ( 70 .3 5± 2 .98vs 68.5 7± 2 .3 6) ,差异无显著性 (P >0 .0 5 )。
短句来源
     Results Followed up 6 months to 15 years, 70 cases with prednisone treatment were cured (74.5%), which meaned the hemangioma was totally removed and no recurrence in 6 months follow up, 51 cases with laser treatment were cured (50%), while in the plastic surgery operation group, the cure rate was 98.6% (68 cases).
     结果 随访 6个月~ 15年 ,其中强的松治疗组治愈 70例 (占 74.5 % ) ,有效 13例 (占 13.8% ) ; 激光治疗组治愈 5 1例(占 5 0 % ) ,有效 41例 (占 40 .2 % ) ;
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     Methods: Based on the animal model of immunity infertility, seventy five pairs of Newzealand rabbits were divided into three groups: YKL treatment group (sub divided into mini , midi and maxi dosage groups), prednisone treatment group and non treatment group.
     方法 :在建立AsAb介导的免疫性不育动物模型的基础上 ,将新西兰兔随机分为 4组 ,即抑抗灵治疗组 ,强的松治疗组 ,未治疗组及阴性对照组。
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  激素治疗
     Results Before prednisone treatment,the serum levels of IL-6 in the steroid-responsive group(118.74±31.18 ng/L) and steroid-resistant group(129.62±28.14 ng/L) were significantly higher than those in the normal controls(35.13±16.21 ng/L)(P<0.05).
     结果激素治疗前,激素敏感组和激素耐药组血IL-6分别为118.74±31.18 ng/L和129.62±28.14 ng/L,均较对照组35.13±16.21 ng/L显著升高(P<0.05),激素敏感组和激素耐药组之间比较差异无显著性(P>0.05)。
短句来源
     Results After the treatment stage of CNS with full dose prednisone,the con-centration of urinary DPD was significantly higher than that in controls,before pred-nisone treatment stage,during reducing dose prednisone treatment stage and after stop-ping treatment stage of CNS respectively (P<0.01,P<0.01,P<0.05,P<0.01).
     结果肾病综合征患儿激素足量治疗后,其尿脱氧吡啶啉水平较正常对照组、激素治疗前、激素减量治疗后及激素停用后均显著升高,差异具有显著性意义(P<0.01,P<0.01,P<0.05,P<0.01)。
短句来源
     The sensibility to prednisone treatment was lower in the elder group, but the recurrence rate of nephrotic syndrome was obviously lower, 11.1% to 43% .
     老年组对激素治疗的敏感性略差; 但NS复发率明显减少,11.1%比43%。
短句来源
     24h urinary calcium lacked specificity as a guideline of evaluating bone resorption activity during the stage of prednisone treatment.
     激素治疗期间24h尿钙作为评价骨吸收的指标缺乏特异性。
短句来源
     The ACA IgG rate was significantly decreaced by prednisone treatment,the ACA IgG positive rate of the children with VMC were significantly higher than that of normal children,and were siginificantly decreased after treatment.
     VCM患儿 ACA Ig G阳性率显著升高 ,治疗 1个月后阳性率显著下降 ,以激素治疗组下降明显。
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  泼尼松
     prednisone treatment group was significantly lower than those in herbal decoction+ prednisone treatment group ( P <0 001) ②SIL2R content:Nontreatment group was significantly higher than those in normal control group( P <0 001) and treatment group( P <0 001);
     泼尼松组低于中药 +泼尼松组 (P<0 .0 0 1)。 2 SIL 2 R含量 :未治疗组高于正常对照组 (P<0 .0 0 1)和治疗组 (P<0 .0 0 1) ;
短句来源
     Conclusion Both moxibustion at Feishu (BL 13) and Gaohuang (BL 43), and prednisone treatment can significantly suppress the expression of TGF-β1mRNA in the pulmonary tissue in the rat of bleomycin-induced pulmonary fibrosis.
     结论:艾灸“肺俞”“膏肓”与泼尼松治疗均能显著抑制肺纤维化大鼠肺组织TGFβ1mRNA表达。
短句来源
     40 Wistar rats were randomized into sham operation control group(given saline),model group(given saline),prednisone treatment group,Qihong decoction treatment group(n=10).
     将40只Wistar大鼠随机分为4组:假手术组、模型组、泼尼松治疗组、芪红合剂治疗组,每组10只。
短句来源
     Objective To explore the changes of the bone density and metabolic makers in patients with systemic lupus erythematosus(SLE) after long-time prednisone treatment.
     目的:观察系统性红斑狼疮(SLE)经长期泼尼松治疗后骨密度及骨代谢生化指标的变化。
短句来源
     Changes of bone density and bone metabolic markers in patients with lupus nephritis after prednisone treatment
     狼疮肾炎泼尼松治疗后骨密度及骨代谢指标的变化
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  “prednisone treatment”译为未确定词的双语例句
     [Results]Twenty two patients responded sensitively to prednisone, whose urinary TGF-β1 was decreased after complete remission by prednisone treatment[(363.8±187.6) vs (234.5±113.2) ng/mgCr,( P <0.01)].
     【结果】22例激素敏感型患儿治疗后尿TGFβ1水平明显下降[(363.8±187.6)vs(234.5±113.2)ng/mgCr,(P<0.01)]。
短句来源
     82.6% of the patients had excellent results with prednisone treatment.
     82 6 %的患者经强的松治疗效果良好。
短句来源
     Results After treatment,the CD8 positive percent of patients of sipulin and prednisone treatment group was distinctly lower than the contrast group,CD+4/CD+8 value was remarkably higher than the contrast group(P<0.05),NK cytoactive percent was a little bit higher than the contrast group(P>005).
     结果治疗组治疗后患者CD8阳性百分率明显低于对照组、CD+4/CD+8值显著高于对照组(P<0.05),NK细胞活性百分率略高于对照组(P>0.05)。
短句来源
     (2) Serum level of IL-12, IFN-γ in the asthma attack group were significantly lower than that in the normal control group after prednisone treatment (P<0.01);
     IL-12,IFN-γ水平分别在急性发作治疗前较治疗后、健康对照组为低(P<0.01)。
短句来源
     Results (1) Serum level of IL-18 in the asthma attack group was significantly higher than that in the normal control group after prednisone treatment (P<0.01);
     结果IL-18水平急性发作期治疗前较治疗后、健康对照组为高(P<0.01)。
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  prednisone treatment
First, in each case a long-term prednisone treatment was administered.
      
Supression of fetal hematopoeitic development by prednisone treatment of pregnant rats
      
Suppression of DNA synthesis in phytohaemagglutinin stimulated lymphocytes by prednisone treatment
      
The aim of our study was to evaluate BMD in premenopausal and postmenopausal sarcoidosis patients with or without prednisone treatment and to compare their BMD values with those of a control group having the same menopausal status.
      
Protein-Losing enteropathy after the modified fontan operation: Oral prednisone treatment with biopsy and laboratory proved impr
      
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Based on an analysis of prednisone treatment in 20 cases of pemphigus, the authors suggested that the dosage of prednisone be determined according to the extent of skin involvement. For mild cases with lesions involved less than 1/3 skin surface, the initial control dosage is recommended to be 60-70mg prednisone a day. For moderately severe cases with lesions involved 2/3 skin surface, the initial control dosage is recommended to be 80-100 mg a day. For severe cases with lesions involved more...

Based on an analysis of prednisone treatment in 20 cases of pemphigus, the authors suggested that the dosage of prednisone be determined according to the extent of skin involvement. For mild cases with lesions involved less than 1/3 skin surface, the initial control dosage is recommended to be 60-70mg prednisone a day. For moderately severe cases with lesions involved 2/3 skin surface, the initial control dosage is recommended to be 80-100 mg a day. For severe cases with lesions involved more than 2/3 skin surface, the initial control dosage is recommended to be 110 - 150 mg a day or a little more. Good effects werc obtained in 4 cases treated with combining prednisone with cyclophosphamide. No effect was obtained in 3 cases treated with combining prednisone with azathioprine. When the persistent erosion and ulcer in the mouth and vulva and recurrent vesicles, bullae on the chest and the back occurred for a long period, pemphigus should be considered. The authors suggest that some laboratorial examinations be made for the early diagnosis.

作者根据强的松治疗20例天疱疮的疗效分析,建议应按病情轻重分三度:轻度者皮疹少于体表面积1/3者,初期控制量60~77mg/天;中度指皮疹约占体表面积2/3者,用量80~100mg/天;重度指皮疹超过体表面积2/3者,用量110~150mg/天或更大。4例加用环磷酰胺者获得良效,而3例加用硫唑嘌呤者未见任何效果。对口腔及外阴发生经久不愈的糜烂或溃疡以及胸、背等处反复出现水疱者应想到患天疱疮的可能,应作进一步的检查,以便早期确诊。

95 children with nephrotie syndrome were studied. The relation of sex, age, duration of attaek, edema, proteinurla, hematurila, blood pressure, urea nitrogen, plasma proteins, choesterol, immunoglobulin serum C_3, and the pattern of response toprednisone to the clinical cla sification of nephrotic syndrome were discussed. The diagnosis of refractory nephrotic syndrome may be facilitated by refering the following findings.age over 7, repeated appearance of R. B. C. and granular casts in urine, normal or increased...

95 children with nephrotie syndrome were studied. The relation of sex, age, duration of attaek, edema, proteinurla, hematurila, blood pressure, urea nitrogen, plasma proteins, choesterol, immunoglobulin serum C_3, and the pattern of response toprednisone to the clinical cla sification of nephrotic syndrome were discussed. The diagnosis of refractory nephrotic syndrome may be facilitated by refering the following findings.age over 7, repeated appearance of R. B. C. and granular casts in urine, normal or increased serum γ-globulin but diminution of C_3, persistence of abnormality in plasma proteins even after 4-8 weeks of prednisone treatment. Various infections are important factor, which usually made the treatment of nephrotic syndrome difficult.

本文对95例肾病综合征进行分析,探讨了性别、年龄、发病迁延时间、浮肿、蛋白尿、血尿、血压、尿素氮、血浆蛋白、血浆胆固醇、免疫球蛋白、补体C_3与激素反应及分型的关系。认为下列综合分析可做为判定难治性肾病综合征的参考。难治性肾病多分布在7岁以上,激素治疗4~8周血浆蛋白尚未恢复,尿镜检反复出现红细胞及颗粒管型,血清r—球蛋白不低,而补体C_3降低,提示难治性肾病。各种感染常常是造成肾病综合心难以控制,甚至死亡的重要因素。

Polyglandular autoimmune syndrome (PAS) is characterized by the dysfunction of the endocrine gland associated with other organ autoimmune disorders. There are three types: PAS type I: chief disorder-hypoparathyroidism; type Ⅱ: chief disorder-adrenal insufficiency; type Ⅲ: autoimmune thyroiditis without Addison's disease but with one or more other autoimmune diseasesRecently, the incidence of autoiommune disease involving nonendocrine organs has increased Lymphocytic infiltration is a prominent pathologic feature...

Polyglandular autoimmune syndrome (PAS) is characterized by the dysfunction of the endocrine gland associated with other organ autoimmune disorders. There are three types: PAS type I: chief disorder-hypoparathyroidism; type Ⅱ: chief disorder-adrenal insufficiency; type Ⅲ: autoimmune thyroiditis without Addison's disease but with one or more other autoimmune diseasesRecently, the incidence of autoiommune disease involving nonendocrine organs has increased Lymphocytic infiltration is a prominent pathologic feature of the organ involved.In this article, the authors report on ten cases of PAS-type Ⅲ. Five of the patients were associated with two autoimmune diseases and five cases were associated with three manifestations. Thyroid hormone and low dose prednisone treatment resulted in satisfactory improvement.

多腺体自身免疫综合征为以一种内分泌腺功能障碍为主,而同时并有其它内分泌或非分泌器官自身免疫疾患的综合征。临床分为3型:PAS I型以甲状旁腺功能低下为主;Ⅱ型以阿迪森氏病为主,Ⅲ型以自身免疫性甲状腺炎为主病。PAS合并非内分泌器官病变目增。淋巴细胞浸润为其主要病理变化。本文报告PASⅢ型10例。2病并发者5例;3病并发者5例。经强地松及/或甲状腺片治疗后均缓解。

 
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