LEADER 01902nam 2200433 450 001 9910688217703321 005 20230629190301.0 035 $a(CKB)5400000000042362 035 $a(NjHacI)995400000000042362 035 $a(EXLCZ)995400000000042362 100 $a20230629d2021 uy 0 101 0 $aeng 135 $aur||||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aPheochromocytoma, Paraganglioma and Neuroblastoma /$fedited by Pasquale Cianci, Enrico Restini and Amit Agrawal 210 1$aLondon :$cIntechOpen,$d2021. 210 4$dİ2021 215 $a1 online resource (xi, 130 pages) $cillustrations 311 $a1-83968-949-8 320 $aIncludes bibliographical references. 330 $aPheochromocytoma, paraganglioma and neuroblastoma are the most common neural crest-derived tumors in adults and children, respectively. These neoplasms are associated with significant morbidity and mortality. Some international studies currently underway are researching and evaluating the presence of any similarities and differences between these tumors. Hopefully, future results will reveal several potential novel genes and pathways that might have major roles in the pathogenesis and progression of these neoplasms. This book discusses epidemiology, genetics, and treatment of these malignancies. 606 $aNeuroblastoma 606 $aNonchromaffin paraganglioma 606 $aPheochromocytoma 615 0$aNeuroblastoma. 615 0$aNonchromaffin paraganglioma. 615 0$aPheochromocytoma. 676 $a616.9948 702 $aCianci$b Pasquale 702 $aRestini$b Enrico 702 $aAgrawal$b Amit 801 0$bNjHacI 801 1$bNjHacl 906 $aBOOK 912 $a9910688217703321 996 $aPheochromocytoma, Paraganglioma and Neuroblastoma$92823108 997 $aUNINA