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10.1016/j.urology.2014.01.007 http://scihub22266oqcxt.onion/10.1016/j.urology.2014.01.007 C4572836!4572836!24642075     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Urology 2014 ; 83 (6): 1225-32 Nephropedia Template TP {{tp|p=24642075|t=2014. The Genetic Basis of Pheochromocytoma and Paraganglioma: Implications for Management |pdf=|usr=}}{{24642075}} gab.com Text The Genetic Basis of Pheochromocytoma and Paraganglioma: Implications for Management JO: Urology http://www.kidney.de/pget.php?&tw=1&pmid=24642075 #FOAvip Chromaffin cells are catecholamine-producing cells derived from neural crest tissue. Chromaffin tumors (ChT) are rare tumors arising from these cells and are divided into pheochromocytoma (PCC) arising from adrenal tissue and paraganglioma (PGL) arising from extra-adrenal ganglia. Previously, ?10% were believed to be hereditary, but advances in genome sequencing has shown roughly 35% of apparently sporadic tumors have a hereditary component. In this review we describe both classic and newly discovered hereditary ChT syndromes and provide recommendations for genetic testing. In many cases the genes associated with these conditions are linked to common kidney cancer pathways familiar to urologic oncologists. Twit Text FOAVip The Genetic Basis of Pheochromocytoma and Paraganglioma: Implications for Management ????Urology http://www.kidney.de/pget.php?&tw=1&pmid=24642075 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24642075 #FOAvip English Wikipedia <ref>{{Cite pmid|24642075}}</ref> The Genetic Basis of Pheochromocytoma and Paraganglioma: Implications for Management #MMPMID24642075 Shuch B; Ricketts CJ; Pacak K; Linehan WM Urology 2014[Jun]; 83 (6): 1225-32 PMID24642075show ga Chromaffin cells are catecholamine-producing cells derived from neural crest tissue. Chromaffin tumors (ChT) are rare tumors arising from these cells and are divided into pheochromocytoma (PCC) arising from adrenal tissue and paraganglioma (PGL) arising from extra-adrenal ganglia. Previously, ?10% were believed to be hereditary, but advances in genome sequencing has shown roughly 35% of apparently sporadic tumors have a hereditary component. In this review we describe both classic and newly discovered hereditary ChT syndromes and provide recommendations for genetic testing. In many cases the genes associated with these conditions are linked to common kidney cancer pathways familiar to urologic oncologists. äThe Genetic Basis of Pheochromocytoma and Paraganglioma: Implications (epmc).pdf DeepDyve Pubget Overpricing