02592nam 22005654a 450 991014574610332120170815111930.01-281-06935-397866110693530-470-69219-70-470-76638-7(CKB)1000000000412267(EBL)320097(OCoLC)476116674(SSID)ssj0000220769(PQKBManifestationID)11174020(PQKBTitleCode)TC0000220769(PQKBWorkID)10143462(PQKB)10090398(MiAaPQ)EBC320097(EXLCZ)99100000000041226720070108d2007 uy 0engur|n|---|||||txtccrPheochromocytoma[electronic resource] diagnosis, localization, and treatment /Karel Pacak, Jacques W.M. Lenders, Graeme EisenhoferMalden, MA ;Oxford Blackwell Pub.20071 online resource (184 p.)Description based upon print version of record.1-4051-4950-7 Includes bibliographical references and index.Historical comments -- Pathology -- Clinical presentation of pheochromocytoma -- Current trends in genetics of pheochromocytoma -- Catecholamines and adrenergic receptors -- Current trends in biochemical diagnosis of pheochromocytoma -- Current trends in localization of pheochromocytoma -- Treatment of pheochromocytoma -- Future trends and perspectives.Pheochromocytomas are rare but treacherous catecholamine-producing tumors, which if missed or not properly treated, will almost invariably prove fatal. Prompt diagnosis is, therefore, essential for effective treatment, usually by surgical resection. The manifestations are diverse and the tumor can mimic a variety of conditions, often resulting in either erroneous diagnoses or a delayed diagnosis. Reflecting the recent leaps in understanding this condition, Pheochromocytoma: Diagnosis, Localization, and Treatment provides a comprehensive update on the improvements in the diagnosis, locPheochromocytomaElectronic books.Pheochromocytoma.616.99616.99445Pacak Karel881323Lenders Jacques W. M881324Eisenhofer Graeme881325MiAaPQMiAaPQMiAaPQBOOK9910145746103321Pheochromocytoma1968252UNINA