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10.1017/erm.2017.8 http://scihub22266oqcxt.onion/10.1017/erm.2017.8 C5687181!5687181!28716159     free     free     free Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Expert+Rev+Mol+Med 2017 ; 19 (ä): ä Nephropedia Template TP {{tp|p=28716159|t=2017. Bilateral Wilms tumour: a review of clinical and molecular features |pdf=|usr=}}{{28716159}} gab.com Text Bilateral Wilms tumour: a review of clinical and molecular features JO: Expert Rev Mol Med http://www.kidney.de/pget.php?&tw=1&pmid=28716159 #FOAvip Wilms tumour (WT) is the most common paediatric kidney cancer and affects approximately one in 10 000 children. The tumour is associated with undifferentiated embryonic lesions called nephrogenic rests (NRs) or, when diffuse, nephroblastomatosis. WT or NRs can occur in both kidneys, termed bilateral disease, found in only 5?8% of cases. Management of bilateral WT presents a major clinical challenge in terms of maximising survival, preserving renal function and understanding underlying genetic risk. In this review, we compile clinical data from 545 published cases of bilateral WT and discuss recent progress in understanding the molecular basis of bilateral WT and its associated precursor NRs in the context of the latest radiological, surgical and epidemiological features. Twit Text FOAVip Bilateral Wilms tumour: a review of clinical and molecular features ????Expert Rev Mol Med http://www.kidney.de/pget.php?&tw=1&pmid=28716159 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28716159 #FOAvip English Wikipedia <ref>{{Cite pmid|28716159}}</ref> Bilateral Wilms tumour: a review of clinical and molecular features #MMPMID28716159 Charlton J; Irtan S; Bergeron C; Pritchard-Jones K Expert Rev Mol Med 2017[]; 19 (ä): ä PMID28716159show ga Wilms tumour (WT) is the most common paediatric kidney cancer and affects approximately one in 10 000 children. The tumour is associated with undifferentiated embryonic lesions called nephrogenic rests (NRs) or, when diffuse, nephroblastomatosis. WT or NRs can occur in both kidneys, termed bilateral disease, found in only 5?8% of cases. Management of bilateral WT presents a major clinical challenge in terms of maximising survival, preserving renal function and understanding underlying genetic risk. In this review, we compile clinical data from 545 published cases of bilateral WT and discuss recent progress in understanding the molecular basis of bilateral WT and its associated precursor NRs in the context of the latest radiological, surgical and epidemiological features. äBilateral Wilms tumour: a review of clinical and molecular features (epmc).pdf DeepDyve Pubget Overpricing