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10.12861/jrip.2015.21 http://scihub22266oqcxt.onion/10.12861/jrip.2015.21 C4594213!4594213!26468484     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26468484&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26468484.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       J+Renal+Inj+Prev 2015 ; 4 (3): 104-6 Nephropedia Template TP {{tp|p=26468484|t=2015. From headache to kidney tumor; an example of von Hippel- Lindau disease |pdf=|usr=}}{{26468484}} gab.com Text From headache to kidney tumor; an example of von Hippel- Lindau disease JO: J Renal Inj Prev http://www.kidney.de/pget.php?&tw=1&pmid=26468484 #FOAvip Background: von Hippel-Lindau disease (VHL) is a rare genetic condition caused by the mutation of the VHL tumor suppressor gene and predisposing to various benign or malignant tumors involving mainly central nervous system (CNS) and retinal hemangioblastomas (RHB). Although considered as occult, multiple renal cysts and renal cell carcinoma (RCC) are frequent in VHL, occurring in nearly two-thirds of patients. RCC is the major neoplasm and the main cause of death in patients with this condition. Case: In this report, we present a case of an occult kidney tumor revealed by neurological symptoms of cerebellar hemangioblastoma. Conclusion: Kidney tumor was diagnosed incidentally on abdominal tomography and confirmed by histopathology analysis. Twit Text FOAVip From headache to kidney tumor; an example of von Hippel- Lindau disease ????J Renal Inj Prev http://www.kidney.de/pget.php?&tw=1&pmid=26468484 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26468484 #FOAvip English Wikipedia <ref>{{Cite pmid|26468484}}</ref> From headache to kidney tumor; an example of von Hippel- Lindau disease #MMPMID26468484 Asserraji M; El Kharras A J Renal Inj Prev 2015[]; 4 (3): 104-6 PMID26468484show ga Background: von Hippel-Lindau disease (VHL) is a rare genetic condition caused by the mutation of the VHL tumor suppressor gene and predisposing to various benign or malignant tumors involving mainly central nervous system (CNS) and retinal hemangioblastomas (RHB). Although considered as occult, multiple renal cysts and renal cell carcinoma (RCC) are frequent in VHL, occurring in nearly two-thirds of patients. RCC is the major neoplasm and the main cause of death in patients with this condition. Case: In this report, we present a case of an occult kidney tumor revealed by neurological symptoms of cerebellar hemangioblastoma. Conclusion: Kidney tumor was diagnosed incidentally on abdominal tomography and confirmed by histopathology analysis. �From headache to kidney tumor; an example of von Hippel- Lindau diseas(epmc).pdf DeepDyve Pubget Overpricing