{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,28]],"date-time":"2026-03-28T08:30:11Z","timestamp":1774686611471,"version":"3.50.1"},"reference-count":70,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2009,1,1]],"date-time":"2009-01-01T00:00:00Z","timestamp":1230768000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2009,1,1]],"date-time":"2009-01-01T00:00:00Z","timestamp":1230768000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Hormones"],"published-print":{"date-parts":[[2009,1]]},"DOI":"10.14310\/horm.2002.1219","type":"journal-article","created":{"date-parts":[[2014,1,29]],"date-time":"2014-01-29T13:20:11Z","timestamp":1391001611000},"page":"29-38","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":37,"title":["Familial pheochromocytoma"],"prefix":"10.1007","volume":"8","author":[{"given":"Zoran","family":"Erlic","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hartmut P. H.","family":"Neumann","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2009,1,1]]},"reference":[{"key":"8010029_CR1","doi-asserted-by":"publisher","DOI":"10.1007\/978-1-4612-5668-7","volume-title":"Anatomy and topography. In The Paraganglionic Chemoreceptor System","author":"F Zak","year":"1982","unstructured":"Zak F, Lawson W 1982 Anatomy and topography. In The Paraganglionic Chemoreceptor System. Springer-Verlag."},{"key":"8010029_CR2","doi-asserted-by":"publisher","first-page":"617","DOI":"10.1136\/jmg.39.9.617","volume":"39","author":"BE Baysal","year":"2002","unstructured":"Baysal BE, 2002 Hereditary paraganglioma targets diverse paraganglia. J Med Genet 39: 617\u2013622.","journal-title":"J Med Genet"},{"key":"8010029_CR3","volume-title":"Pheochromocytoma. In Harrison\u2019s Principles of Internal Medicine","author":"H Neumann","year":"2008","unstructured":"Neumann H 2008 Pheochromocytoma. In Harrison\u2019s Principles of Internal Medicine, The McGraw-Hill Companies, Inc; New York"},{"key":"8010029_CR4","volume-title":"WHO Classification of Tumours, Pathology and genetics of tumours of endocrine organs Lyon","author":"RA DeLellis","year":"2004","unstructured":"DeLellis RA, Lloyd RV, Heitz PU, Eng C, 2004 World Health Organization (2004) WHO Classification of Tumours, Pathology and genetics of tumours of endocrine organs Lyon, IARC Press."},{"key":"8010029_CR5","doi-asserted-by":"publisher","first-page":"13","DOI":"10.1097\/01.cco.0000147900.12325.d9","volume":"17","author":"H Yeo","year":"2005","unstructured":"Yeo H, Roman S, 2005 Pheochromocytoma and functional paraganglioma. Curr Opin Oncol 17: 13\u201318.","journal-title":"Curr Opin Oncol"},{"key":"8010029_CR6","doi-asserted-by":"publisher","first-page":"651","DOI":"10.1007\/BF03345810","volume":"15","author":"C Proye","year":"1992","unstructured":"Proye C, Vix M, Goropoulos A, Kerlo P, Lecomte-Houcke M, 1992 High incidence of malignant pheochromocytoma in a surgical unit. 26 cases out of 100 patients operated from 1971 to 1991. J Endocrinol Invest 15: 651\u2013663.","journal-title":"J Endocrinol Invest"},{"key":"8010029_CR7","doi-asserted-by":"publisher","first-page":"1987","DOI":"10.1002\/1097-0142(197711)40:5<1987::AID-CNCR2820400502>3.0.CO;2-R","volume":"40","author":"MM Melicow","year":"1977","unstructured":"Melicow MM, 1977 One hundred cases of pheochromocytoma (107 tumours) at the Columbia-Presbyterian Medical Center, 1926\u20131976: a clinicopathological analysis. Cancer 40: 1987\u20132004.","journal-title":"Cancer"},{"key":"8010029_CR8","doi-asserted-by":"publisher","first-page":"551","DOI":"10.1097\/00000478-200205000-00002","volume":"26","author":"LD Thompson","year":"2002","unstructured":"Thompson LD, 2002 Pheochromocytoma of the Adrenal gland Scaled Score (PASS) to separate benign from malignant neoplasms: a clinicopathologic and immunophenotypic study of 100 cases. Am J Surg Pathol 26: 551\u2013566.","journal-title":"Am J Surg Pathol"},{"key":"8010029_CR9","doi-asserted-by":"publisher","first-page":"4865","DOI":"10.1210\/jc.2007-1253","volume":"92","author":"E Thouennon","year":"2007","unstructured":"Thouennon E, Elkahloun AG, Guillemot J, et al, 2007 Identification of potential gene markers and insights into the pathophysiology of pheochromocytoma malignancy. J Clin Endocrinol Metab 92: 4865\u20134872.","journal-title":"J Clin Endocrinol Metab"},{"key":"8010029_CR10","doi-asserted-by":"publisher","first-page":"329","DOI":"10.1007\/s12022-006-0004-2","volume":"17","author":"AM McNicol","year":"2006","unstructured":"McNicol AM, 2006 Histopathology and immunohisto-chemistry of adrenal medullary tumours and paragangliomas. Endocr Pathol 17: 329\u2013336.","journal-title":"Endocr Pathol"},{"key":"8010029_CR11","doi-asserted-by":"publisher","first-page":"1459","DOI":"10.1056\/NEJMoa020152","volume":"346","author":"HP Neumann","year":"2002","unstructured":"Neumann HP, Bausch B, McWhinney SR, et al, 2002 Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 346: 1459\u20131466.","journal-title":"N Engl J Med"},{"issue":"14","key":"8010029_CR12","first-page":"1686","volume":"292","author":"HP Neumann","year":"2004","unstructured":"Neumann HP, Pawlu C, Peczkowska M, et al, 2004 Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. [erratum appears in JAMA. 2004 Oct 13;292(14): 1686]. JAMA 292: 943\u2013951.","journal-title":"JAMA"},{"key":"8010029_CR13","doi-asserted-by":"publisher","first-page":"111","DOI":"10.1038\/ncpendmet0726","volume":"4","author":"M Peczkowska","year":"2008","unstructured":"Peczkowska M, Cascon A, Prejbisz A, et al, 2008 Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation. Nat Clin Pract Endocrinol Metab 4: 111\u2013115.","journal-title":"Nat Clin Pract Endocrinol Metab"},{"key":"8010029_CR14","doi-asserted-by":"publisher","first-page":"8812","DOI":"10.1200\/JCO.2005.03.1484","volume":"23","author":"L Amar","year":"2005","unstructured":"Amar L, Bertherat J, Baudin E, et al, 2005 Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 23: 8812\u20138818.","journal-title":"J Clin Oncol"},{"key":"8010029_CR15","doi-asserted-by":"publisher","first-page":"244","DOI":"10.1007\/BF01938677","volume":"103","author":"F Fr\u00e4nkel","year":"1886","unstructured":"Fr\u00e4nkel F, 1886 Ein Fall von doppelseitigem, v\u00f6llig latent verlaufenen Nebennierentumor und gleichzeitiger Nephritis mit Ver\u00e4nderungen am Circulationsapparat und Retinits. Virchows Archiv f\u00fcr Pathologie, Anatomie und Physiologie 103: 244\u2013263.","journal-title":"Virchows Archiv f\u00fcr Pathologie, Anatomie und Physiologie"},{"key":"8010029_CR16","doi-asserted-by":"publisher","first-page":"1311","DOI":"10.1056\/NEJMoa071407","volume":"357","author":"H M Neumann","year":"2007","unstructured":"Neumann HP MD, Alexander Vortmeyer, Dieter Schmidt, et al, 2007 Evidence for MEN 2 in the Original Description of Classic Pheochromocytoma. N Engl J Med 357: 1311\u20131315.","journal-title":"N Engl J Med"},{"key":"8010029_CR17","first-page":"1623","volume":"47","author":"S Suzuki","year":"1910","unstructured":"Suzuki S, 1910 \u00dcber zwei Tumoren aus Nebennierenmark-gewebe. Berliner Klinische Wochenschrift 47: 1623.","journal-title":"Berliner Klinische Wochenschrift"},{"key":"8010029_CR18","doi-asserted-by":"publisher","first-page":"1531","DOI":"10.1056\/NEJM199311183292103","volume":"329","author":"HP Neumann","year":"1993","unstructured":"Neumann HP, Berger DP, Sigmund G, et al, 1993 Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease. N Engl J Med 329: 1531\u20131538.","journal-title":"N Engl J Med"},{"key":"8010029_CR19","doi-asserted-by":"publisher","first-page":"848","DOI":"10.1126\/science.287.5454.848","volume":"287","author":"BE Baysal","year":"2000","unstructured":"Baysal BE, Ferrell RE, Willett-Brozick JE, et al, 2000 Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 287: 848\u2013851.","journal-title":"Science"},{"key":"8010029_CR20","doi-asserted-by":"publisher","first-page":"49","DOI":"10.1086\/321282","volume":"69","author":"D Astuti","year":"2001","unstructured":"Astuti D, Latif F, Dallol A, et al, 2001 Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am J Hum Genet 69: 49\u201354.","journal-title":"Am J Hum Genet"},{"key":"8010029_CR21","doi-asserted-by":"publisher","first-page":"586","DOI":"10.1136\/jmg.2007.051045","volume":"44","author":"M Mannelli","year":"2007","unstructured":"Mannelli M, Ercolino T, Giache V, Simi L, Cirami C, Parenti G, 2007 Genetic screening for pheochromocytoma: should SDHC gene analysis be included? J Med Genet 44: 586\u2013587.","journal-title":"J Med Genet"},{"key":"8010029_CR22","doi-asserted-by":"publisher","first-page":"1609","DOI":"10.1210\/jc.2007-1989","volume":"93","author":"P Pigny","year":"2008","unstructured":"Pigny P, Vincent A, Cardot Bauters C, et al, 2008 Paraganglioma after maternal transmission of a succinate dehydrogenase gene mutation. J Clin Endocrinol Metab 93: 1609\u20131615.","journal-title":"J Clin Endocrinol Metab"},{"key":"8010029_CR23","doi-asserted-by":"publisher","first-page":"1573","DOI":"10.1210\/jc.2008-0569","volume":"93","author":"HP Neumann","year":"2008","unstructured":"Neumann HP, Erlic Z, 2008 Maternal Transmission of Symptomatic Disease with SDHD Mutation: Fact or Fiction? J Clin Endocrinol Metab 93: 1573\u20131575.","journal-title":"J Clin Endocrinol Metab"},{"key":"8010029_CR24","doi-asserted-by":"publisher","first-page":"149","DOI":"10.1196\/annals.1353.015","volume":"1073","author":"G Opocher","year":"2006","unstructured":"Opocher G, Schiavi F, Iacobone M, et al, 2006 Familial nonsyndromic pheochromocytoma. Ann N Y Acad Sci 1073: 149\u2013155.","journal-title":"Ann N Y Acad Sci"},{"key":"8010029_CR25","doi-asserted-by":"publisher","first-page":"9651","DOI":"10.1158\/0008-5472.CAN-05-1427","volume":"65","author":"PL Dahia","year":"2005","unstructured":"Dahia PL, Hao K, Rogus J, et al, 2005 Novel pheochromocytoma susceptibility loci identified by integrative genomics. Cancer Res 65: 9651\u20139658.","journal-title":"Cancer Res"},{"key":"8010029_CR26","doi-asserted-by":"publisher","first-page":"181","DOI":"10.1126\/science.2134734","volume":"249","author":"MR Wallace","year":"1990","unstructured":"Wallace MR, Marchuk DA, Andersen LB, et al, 1990 Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. Science 249: 181\u2013186.","journal-title":"Science"},{"key":"8010029_CR27","doi-asserted-by":"publisher","first-page":"1617","DOI":"10.1056\/NEJM198112313052704","volume":"305","author":"VM Riccardi","year":"1981","unstructured":"Riccardi VM, 1981 Von Recklinghausen neurofibromatosis. N Engl J Med 305: 1617\u20131627.","journal-title":"N Engl J Med"},{"key":"8010029_CR28","doi-asserted-by":"publisher","first-page":"13","DOI":"10.1007\/s10689-004-6128-y","volume":"4","author":"G Opocher","year":"2005","unstructured":"Opocher G, Conton P, Schiavi F, Macino B, Mantero F, 2005 Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1. Fam Cancer 4: 13\u201316.","journal-title":"Fam Cancer"},{"key":"8010029_CR29","doi-asserted-by":"publisher","first-page":"2729","DOI":"10.1056\/NEJMc066006","volume":"354","author":"B Bausch","year":"2006","unstructured":"Bausch B, Borozdin W, Neumann HPH, 2006 European-American Pheochromocytoma Study G. Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma. N Engl J Med 354: 2729\u20132731.","journal-title":"N Engl J Med"},{"key":"8010029_CR30","doi-asserted-by":"publisher","first-page":"3999","DOI":"10.1210\/jc.2005-0064","volume":"90","author":"A Machens","year":"2005","unstructured":"Machens A, Brauckhoff M, Holzhausen HJ, Thanh PN, Lehnert H, Dralle H, 2005 Codon-specific development of pheochromocytoma in multiple endocrine neoplasia type 2. J Clin Endocrinol Metab 90: 3999\u20134003.","journal-title":"J Clin Endocrinol Metab"},{"key":"8010029_CR31","doi-asserted-by":"publisher","first-page":"800","DOI":"10.1016\/j.surg.2007.09.013","volume":"142","author":"FJ Quayle","year":"2007","unstructured":"Quayle FJ, Fialkowski EA, Benveniste R, Moley JF, 2007 Pheochromocytoma penetrance varies by RET mutation in MEN 2A. Surgery 142: 800\u2013805.","journal-title":"Surgery"},{"key":"8010029_CR32","doi-asserted-by":"publisher","first-page":"1052","DOI":"10.1016\/0140-6736(91)91705-Y","volume":"337","author":"HP Neumann","year":"1991","unstructured":"Neumann HP, Wiestler OD, 1991 Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus. [see comment]. Lancet 337: 1052\u20131054.","journal-title":"Lancet"},{"key":"8010029_CR33","doi-asserted-by":"publisher","first-page":"1317","DOI":"10.1126\/science.8493574","volume":"260","author":"F Latif","year":"1993","unstructured":"Latif F, Tory K, Gnarra J, et al, 1993 Identification of the von Hippel-Lindau disease tumor suppressor gene. [see comment]. Science 260: 1317\u20131320.","journal-title":"Science"},{"key":"8010029_CR34","doi-asserted-by":"publisher","first-page":"328","DOI":"10.1136\/jmg.33.4.328","volume":"33","author":"ER Maher","year":"1996","unstructured":"Maher ER, Webster AR, Richards FM, et al, 1996 Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations. J Med Genet 33: 328\u2013332.","journal-title":"J Med Genet"},{"key":"8010029_CR35","doi-asserted-by":"publisher","first-page":"193","DOI":"10.1038\/nrc1013","volume":"3","author":"C Eng","year":"2003","unstructured":"Eng C, Kiuru M, Fernandez MJ, Aaltonen LA, 2003 A role for mitochondrial enzymes in inherited neoplasia and beyond. Nat Rev Cancer 3: 193\u2013202.","journal-title":"Nat Rev Cancer"},{"key":"8010029_CR36","doi-asserted-by":"publisher","first-page":"12","DOI":"10.1186\/1741-7007-5-12","volume":"5","author":"BE Baysal","year":"2007","unstructured":"Baysal BE, Lawrence EC, Ferrell RE, 2007 Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA. BMC Biol 5: 12.","journal-title":"BMC Biol"},{"key":"8010029_CR37","doi-asserted-by":"publisher","first-page":"56","DOI":"10.1007\/BF00225075","volume":"95","author":"EC Mariman","year":"1995","unstructured":"Mariman EC, van Beersum SE, Cremers CW, Struycken PM, Ropers HH, 1995 Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13. 1: evidence for genetic heterogeneity. Hum Genet 95: 56\u201362.","journal-title":"Hum Genet"},{"key":"8010029_CR38","doi-asserted-by":"publisher","first-page":"27","DOI":"10.1007\/s00108-008-2196-7","volume":"50","author":"N Reisch","year":"2009","unstructured":"Reisch N, Walz MK, Erlic Z, Neumann HP, 2009 [Pheochromocytoma \u2014 still a challenge]. Der Internist 50: 27\u201335","journal-title":"Der Internist"},{"key":"8010029_CR39","doi-asserted-by":"publisher","first-page":"827","DOI":"10.1210\/jc.2005-1862","volume":"91","author":"DE Benn","year":"2006","unstructured":"Benn DE, Gimenez-Roqueplo AP, Reilly JR, et al, 2006 Clinical presentation and penetrance of pheochromocytoma\/paraganglioma syndromes. J Clin Endocrinol Metab 91: 827\u2013836.","journal-title":"J Clin Endocrinol Metab"},{"key":"8010029_CR40","doi-asserted-by":"publisher","first-page":"703","DOI":"10.1136\/jmg.2004.019224","volume":"41","author":"BE Baysal","year":"2004","unstructured":"Baysal BE, Willett-Brozick JE, Filho PA, Lawrence EC, Myers EN, Ferrell RE, 2004 An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma. J Med Genet 41: 703\u2013709.","journal-title":"J Med Genet"},{"key":"8010029_CR41","doi-asserted-by":"publisher","first-page":"2057","DOI":"10.1001\/jama.294.16.2057","volume":"294","author":"F Schiavi","year":"2005","unstructured":"Schiavi F, Boedeker CC, Bausch B, et al, 2005 Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. JAMA 294: 2057\u20132063.","journal-title":"JAMA"},{"key":"8010029_CR42","doi-asserted-by":"publisher","first-page":"153","DOI":"10.1086\/381054","volume":"74","author":"S Vanharanta","year":"2004","unstructured":"Vanharanta S, Buchta M, McWhinney SR, et al, 2004 Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. Am J Hum Genet 2004;74: 153\u2013159.","journal-title":"Am J Hum Genet"},{"key":"8010029_CR43","doi-asserted-by":"publisher","first-page":"1054","DOI":"10.1056\/NEJMc071191","volume":"357","author":"SR McWhinney","year":"2007","unstructured":"McWhinney SR, Pasini B, Stratakis CA, 2007 Familial gastrointestinal stromal tumours and germ-line mutations. N Engl J Med 357: 1054\u20131056.","journal-title":"N Engl J Med"},{"key":"8010029_CR44","first-page":"869","volume":"10","author":"PF Plouin","year":"1981","unstructured":"Plouin PF, Degoulet P, Tugaye A, Ducrocq MB, Menard J, 1981 [Screening for phaeochromocytoma: in which hypertensive patients? A semiological study of 2585 patients, including 11 with phaeochromocytoma (author\u2019s transl)]. La Nouvelle presse medicale 10: 869\u2013872.","journal-title":"La Nouvelle presse medicale"},{"key":"8010029_CR45","doi-asserted-by":"publisher","first-page":"681","DOI":"10.1530\/eje.0.1500681","volume":"150","author":"JP Baguet","year":"2004","unstructured":"Baguet JP, Hammer L, Mazzuco TL, Chabre O, et al, 2004 Circumstances of discovery of phaeochromocytoma: a retrospective study of 41 consecutive patients. Eur J Endocrinol 150: 681\u2013686.","journal-title":"Eur J Endocrinol"},{"key":"8010029_CR46","doi-asserted-by":"publisher","first-page":"619","DOI":"10.1530\/eje.0.1410619","volume":"141","author":"M Mannelli","year":"1999","unstructured":"Mannelli M, Ianni L, Cilotti A, Conti A, 1999 Pheochro-mocytoma in Italy: a multicentric retrospective study. Eur J Endocrinol 141: 619\u2013624.","journal-title":"Eur J Endocrinol"},{"key":"8010029_CR47","first-page":"1154","volume":"100","author":"C Proye","year":"1986","unstructured":"Proye C, Fossati P, Fontaine P, et al, 1986 Dopamine-secreting pheochromocytoma: an unrecognized entity? Classification of pheochromocytomas according to their type of secretion. Surgery 100: 1154\u20131162.","journal-title":"Surgery"},{"key":"8010029_CR48","doi-asserted-by":"publisher","first-page":"477","DOI":"10.1007\/s11906-004-0044-2","volume":"6","author":"WM Manger","year":"2004","unstructured":"Manger WM, Eisenhofer G, 2004 Pheochromocytoma: diagnosis and management update. Current Hypertens Rep 6: 477\u2013484.","journal-title":"Current Hypertens Rep"},{"key":"8010029_CR49","volume-title":"Williams Textbook of Endocrinology","author":"WF Young Jr","year":"2008","unstructured":"Young WF Jr 2008 Endocrine hypertension. In Williams Textbook of Endocrinology, Philadelphia, PA, Saunders Elsevier."},{"key":"8010029_CR50","doi-asserted-by":"crossref","unstructured":"Mariola Peczkowska, Zoran Erlic, Michael M. Hoffmann, et al, Impact of Screening Kindreds for SDHD p. Cys11X as a Common Mutation Associated with Paraganglioma Syndrome Type 1. J Clin Endocrinol Metab 93: 4818-4825.","DOI":"10.1210\/jc.2008-1290"},{"key":"8010029_CR51","doi-asserted-by":"publisher","first-page":"1427","DOI":"10.1001\/jama.287.11.1427","volume":"287","author":"JW Lenders","year":"2002","unstructured":"Lenders JW, Pacak K, Walther MM, et al, 2002 Biochemical diagnosis of pheochromocytoma: which test is best? JAMA 287: 1427\u20131434.","journal-title":"JAMA"},{"key":"8010029_CR52","doi-asserted-by":"publisher","first-page":"735","DOI":"10.1373\/clinchem.2004.045484","volume":"51","author":"G Eisenhofer","year":"2005","unstructured":"Eisenhofer G, Lenders JW, Goldstein DS, et al, 2005 Pheochromocytoma catecholamine phenotypes and prediction of tumor size and location by use of plasma free metanephrines. Clin Chem 51: 735\u2013744.","journal-title":"Clin Chem"},{"key":"8010029_CR53","doi-asserted-by":"publisher","first-page":"479","DOI":"10.1210\/jc.2003-031091","volume":"89","author":"I Ilias","year":"2004","unstructured":"Ilias I, Pacak K, 2004 Current approaches and recommended algorithm for the diagnostic localization of pheochromocytoma. J Clin Endocrinol Metab 89: 479\u2013491.","journal-title":"J Clin Endocrinol Metab"},{"key":"8010029_CR54","first-page":"685","volume":"86","author":"E van der Harst","year":"2001","unstructured":"van der Harst E, de Herder WW, Bruining HA, et al, 2001 [(123)I]metaiodobenzylguanidine and [(111)In]octreotide uptake in begnign and malignant pheochromocytomas. J Clin Endocrinol Metab 86: 685\u2013693.","journal-title":"J Clin Endocrinol Metab"},{"key":"8010029_CR55","doi-asserted-by":"publisher","first-page":"119","DOI":"10.1046\/j.1442-2042.1999.06310.x","volume":"6","author":"N Furuta","year":"1999","unstructured":"Furuta N, Kiyota H, Yoshigoe F, Hasegawa N, Ohishi Y, 1999 Diagnosis of pheochromocytoma using [123I]-compared with [131I]-metaiodobenzylguanidine scintigraphy. Int J Urol 6: 119\u2013124.","journal-title":"Int J Urol"},{"key":"8010029_CR56","doi-asserted-by":"publisher","first-page":"689","DOI":"10.1007\/s00259-003-1115-3","volume":"230","author":"S Hoegerle","year":"2003","unstructured":"Hoegerle S, Ghanem N, Altehoefer C, et al, 2003 18F-DOPA positron emission tomography for the detection of glomus tumours. Eur J Nucl Med Mol Imaging 230: 689\u2013694.","journal-title":"Eur J Nucl Med Mol Imaging"},{"key":"8010029_CR57","doi-asserted-by":"publisher","first-page":"507","DOI":"10.1148\/radiol.2222010622","volume":"222","author":"S Hoegerle","year":"2002","unstructured":"Hoegerle S, Nitzsche E, Altehoefer C, et al, 2002 Pheochromocytomas: detection with 18F DOPA whole body PET\u2014initial results. Radiology 222: 507\u2013512.","journal-title":"Radiology"},{"key":"8010029_CR58","doi-asserted-by":"publisher","first-page":"4069","DOI":"10.1210\/jc.2007-1720","volume":"92","author":"K Pacak","year":"2007","unstructured":"Pacak K, 2007 Preoperative management of the pheochromocytoma patient. J Clin Endocrinol Metab 92: 4069\u20134079.","journal-title":"J Clin Endocrinol Metab"},{"key":"8010029_CR59","doi-asserted-by":"publisher","first-page":"728","DOI":"10.1007\/s00268-001-0023-6","volume":"25","author":"MK Walz","year":"2001","unstructured":"Walz MK, Peitgen K, Walz MV, et al, 2001 Posterior retroperitoneoscopic adrenalectomy: lessons learned within five years. World J Surg 25: 728\u2013734.","journal-title":"World J Surg"},{"key":"8010029_CR60","doi-asserted-by":"publisher","first-page":"719","DOI":"10.1002\/bjs.4964","volume":"92","author":"MK Walz","year":"2005","unstructured":"Walz MK, Petersenn S, Koch JA, Mann K, Neumann HP, Schmid KW, 2005 Endoscopic treatment of large primary adrenal tumours. Br J Surg 92: 719\u2013723.","journal-title":"Br J Surg"},{"key":"8010029_CR61","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1007\/s00268-005-0373-6","volume":"30","author":"MK Walz","year":"2006","unstructured":"Walz MK, Alesina PF, Wenger FA, et al, 2006 Laparoscopic and Retroperitoneoscopic Treatment of Pheochromocytomas and Retroperitoneal Paragangliomas: Results of 161 Tumours in 126 Patients. World J Surg 30: 1\u201310.","journal-title":"World J Surg"},{"key":"8010029_CR62","doi-asserted-by":"publisher","first-page":"65","DOI":"10.1007\/s00268-006-0083-8","volume":"31","author":"M Barczynski","year":"2007","unstructured":"Barczynski M, Konturek A, Golkowski F, et al, 2007 Posterior retroperitoneoscopic adrenalectomy: a comparison between the initial experience in the invention phase and introductory phase of the new surgical technique. World J Surg 31: 65\u201371.","journal-title":"World J Surg"},{"key":"8010029_CR63","doi-asserted-by":"publisher","first-page":"525","DOI":"10.1016\/j.jamcollsurg.2003.12.001","volume":"198","author":"L Yip","year":"2004","unstructured":"Yip L, Lee JE, Shapiro SE, et al, 2004 Surgical management of hereditary pheochromocytoma. J Am Coll Surg 198: 525\u2013534","journal-title":"J Am Coll Surg"},{"key":"8010029_CR64","doi-asserted-by":"publisher","first-page":"1323","DOI":"10.1007\/s00268-004-7667-y","volume":"28","author":"MK Walz","year":"2004","unstructured":"Walz MK, Peitgen K, Diesing D, et al, 2004 Partial versus total adrenalectomy by the posterior retroperitoneoscopic approach: early and long-term results of 325 consecutive procedures in primary adrenal neoplasias. World J Surg 28: 1323\u20131329.","journal-title":"World J Surg"},{"key":"8010029_CR65","doi-asserted-by":"publisher","first-page":"1005","DOI":"10.1007\/s00268-002-6632-x","volume":"26","author":"MK Walz","year":"2002","unstructured":"Walz MK, Peitgen K, Neumann HP, Janssen OE, Philipp T, Mann K, 2002 Endoscopic treatment of solitary, bilateral, multiple, and recurrent pheochromocytomas and paragangliomas. World J Surg 26: 1005\u20131012.","journal-title":"World J Surg"},{"key":"8010029_CR66","doi-asserted-by":"publisher","first-page":"956","DOI":"10.1016\/S0039-6060(03)00426-4","volume":"134","author":"SD Safford","year":"2003","unstructured":"Safford SD, Coleman RE, Gockerman JP, et al, 2003 Iodine -131 metaiodobenzylguanidine is an effective treatment for malignant pheochromocytoma and paraganglioma. Surgery 134: 956\u2013962.","journal-title":"Surgery"},{"key":"8010029_CR67","doi-asserted-by":"publisher","first-page":"465","DOI":"10.1196\/annals.1353.050","volume":"1073","author":"PA Fitzgerald","year":"2006","unstructured":"Fitzgerald PA, Goldsby RE, Huberty JP, et al, 2006 Malignant pheochromocytomas and paragangliomas: a phase II study of therapy with high-dose 131I-metaiodobenzylguanidine (131I-MIBG). Ann NY Acad Sci 1073: 465\u2013490.","journal-title":"Ann NY Acad Sci"},{"key":"8010029_CR68","first-page":"334","volume":"52","author":"F Forrer","year":"2008","unstructured":"Forrer F, Riedweg I, Maecke HR, Mueller-Brand J, 2008 Radiolabeled DOTATOC in patients with advanced paraganglioma and pheochromocytoma. Q J Nucl Med Mol Imaging 52: 334\u2013340.","journal-title":"Q J Nucl Med Mol Imaging"},{"key":"8010029_CR69","doi-asserted-by":"publisher","first-page":"406","DOI":"10.1089\/cbr.2006.325","volume":"22","author":"C Wehrmann","year":"2007","unstructured":"Wehrmann C, Senftleben S, Zachert C, Muller D, Baum RP, 2007 Results of individual patient dosimetry in peptide receptor radionuclide therapy with 177Lu DOTA-TATE and 177Lu DOTA-NOC. Cancer Biother Radiopharm 22: 406\u2013416.","journal-title":"Cancer Biother Radiopharm"},{"key":"8010029_CR70","doi-asserted-by":"publisher","first-page":"62","DOI":"10.1111\/j.1524-6175.2002.01452.x","volume":"4","author":"WM Manger","year":"2002","unstructured":"Manger WM, Gifford RW, 2002 Pheochromocytoma. J Clin Hypertens 4: 62\u201372.","journal-title":"J Clin Hypertens"}],"container-title":["Hormones"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.14310\/horm.2002.1219.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.14310\/horm.2002.1219\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.14310\/horm.2002.1219.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,2,9]],"date-time":"2025-02-09T15:34:04Z","timestamp":1739115244000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.14310\/horm.2002.1219"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,1]]},"references-count":70,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2009,1]]}},"alternative-id":["8010029"],"URL":"https:\/\/doi.org\/10.14310\/horm.2002.1219","relation":{},"ISSN":["1109-3099","2520-8721"],"issn-type":[{"value":"1109-3099","type":"print"},{"value":"2520-8721","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,1]]},"assertion":[{"value":"1 November 2008","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"30 November 2008","order":2,"name":"revised","label":"Revised","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"10 December 2008","order":3,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"1 January 2009","order":4,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"This content has been made available to all.","name":"free","label":"Free to read"}]}}