Titlebook: Renal Tumors of Childhood; Biology and Therapy Kathy Pritchard-Jones,Jeffrey S. Dome Book 2014 The Editor(s) (if applicable) and The Author

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书目名称Renal Tumors of Childhood影响因子(影响力)




书目名称Renal Tumors of Childhood影响因子(影响力)学科排名




书目名称Renal Tumors of Childhood网络公开度




书目名称Renal Tumors of Childhood网络公开度学科排名




书目名称Renal Tumors of Childhood被引频次




书目名称Renal Tumors of Childhood被引频次学科排名




书目名称Renal Tumors of Childhood年度引用




书目名称Renal Tumors of Childhood年度引用学科排名




书目名称Renal Tumors of Childhood读者反馈




书目名称Renal Tumors of Childhood读者反馈学科排名

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Genetic Predisposition to Wilms Tumour,mours occur in approximately 5 % of cases, and Wilms tumour has been reported in association with more than 50 different genetic disorders, pointing to an underlying predisposition in further individuals. There is conclusive evidence of an increased risk of Wilms tumour in only a small number of dis

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Clinical Presentation,en. However, specific details of the history, physical exam and laboratory evaluation can raise the suspicion of WT even prior to imaging or surgical procedures. Other renal tumors, such as rhabdoid tumor of the kidney (RTK), congenital mesoblastic nephroma (CMN), clear cell sarcoma of the kidney (C

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Treatment of Wilms Tumour: The SIOP Approach,pre-, intra- and postoperatively as well as chemotherapy were used, and pretreatment prior to surgery was widely accepted. However, the optimum timing of nephrectomy was the subject of lively debate between institutions. The improving imaging modalities and thus reliable radiologic diagnosis of neph

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Molecular-Targeted Therapy for Pediatric Renal Tumors,loped countries, and as such, treatment of Wilms’ tumor is regarded as one of the great successes in pediatric oncology. Without diminishing the import of such progress, it should be noted, however, that universal cure is not a reality and cure rates remain poor in developing countries where the del