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Selective, Antihypertensives, Other. Waguespack SG, Rich T, Grubbs E, Ying AK, Perrier ND, Ayala- Ramirez M, et al. A current review of the etiology, diagnosis, and treatment of pediatric pheochromocytoma and paraganglioma. J Clin Endocrinol Metab. Sheps SG, Jiang NS, Klee GG, van Heerden JA. Recent developments in the diagnosis and treatment of pheochromocytoma. Yeterian EH, Pandya DN. Corticothalamic connections of the superior temporal sulcus in rhesus monkeys. Elenkova A, Matrozova J, Zacharieva S, Kirilov G, Kalinov K. Adiponectin - A possible factor in the pathogenesis of carbohydrate metabolism disturbances in patients with pheochromocytoma. Pheochromocytoma: Update on Disease Management. Ther Adv in Endo and Metab. Cardiovascular manifestations of phaeochromocytoma. Pheochromocytoma of the Adrenal gland Scaled Score (PASS) to separate benign from malignant neoplasms: a clinicopathologic and immunophenotypic study of 1. 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MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma. Neumann HP, Berger DP, Sigmund G, Blum U, Schmidt D, Parmer RJ, et al. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel- Lindau disease. Gergics P, Patocs A, Toth M, Igaz P, Szucs N, Liko I, et al. Germline VHL gene mutations in Hungarian families with von Hippel- Lindau disease and patients with apparently sporadic unilateral pheochromocytomas. Niemann S, Becker- Follmann J, Nurnberg G, Ruschendorf F, Sieweke N, et al. Assignment of PGL3 to chromosome 1 (q. Burnichon N, Briere JJ, Libe R, Vescovo L, Riviere J, et al. SDHA is a tumor suppressor gene causing paraganglioma. SDHAF2 (PGL2- SDH5) and hereditary head and neck paraganglioma. Congenital hemihypertrophy and pheochromocytoma, not a coincidental combination? Beard CM, Sheps SG, Kurland LT, Carney JA, Lie JT. Occurrence of pheochromocytoma in Rochester, Minnesota, 1. The incidentally discovered adrenal mass. Boulkina LS, Newton CA, Drake AJ 3rd, Tanenberg RJ. Acute myocardial infarction attributable to adrenergic crises in a patient with pheochromocytoma and neurofibromatosis 1. Pheochromocytoma and pregnancy: a deceptive connection. Eur J Endocrinol. Feb; 1. 66(2): 1. La Batide- Alanore A, Chatellier G, Plouin PF. Diabetes as a marker of pheochromocytoma in hypertensive patients. Endocrine Society first to address rare adrenal- tumor care. Medscape Medical News. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. The North American Neuroendocrine Tumor Society consensus guideline for the diagnosis and management of neuroendocrine tumors: pheochromocytoma, paraganglioma, and medullary thyroid cancer. Biochemical diagnosis of pheochromocytoma: which test is best? Dietary influences on plasma and urinary metanephrines: implications for diagnosis of catecholamine- producing tumors. J Clin Endocrinol Metab. Jimenez C, Cote G, Arnold A, Gagel RF. Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes? J Clin Endocrinol Metab. Eisenhofer G, Goldstein DS, Walther MM, Friberg P, Lenders JW, Keiser HR, et al. Biochemical diagnosis of pheochromocytoma: how to distinguish true- from false- positive test results. J Clin Endocrinol Metab. Lenders JW, Pacak K, Huynh TT, Sharabi Y, Mannelli M, Bratslavsky G, et al. Low sensitivity of glucagon provocative testing for diagnosis of pheochromocytoma. J Clin Endocrinol Metab. Adrenocortical carcinomas and adrenal pheochromocytomas: mass and enhancement loss evaluation at delayed contrast- enhanced CT. Park BK, Kim CK, Kwon GY, Kim JH. Re- evaluation of pheochromocytomas on delayed contrast- enhanced CT: washout enhancement and other imaging features. Baid SK, Lai EW, Wesley RA, Ling A, Timmers HJ, Adams KT, et al. Brief communication: radiographic contrast infusion and catecholamine release in patients with pheochromocytoma. CT of pheochromocytoma and paraganglioma: risk of adverse events with i. Blake MA, Kalra MK, Maher MM, Sahani DV, Sweeney AT, Mueller PR, et al. Pheochromocytoma: an imaging chameleon. Faria JF, Goldman SM, Szejnfeld J, Melo H, Kater C, Kenney P, et al. Adrenal masses: characterization with in vivo proton MR spectroscopy- -initial experience. Kim S, Salibi N, Hardie AD, Xu J, Lim RP, Lee VS, et al. Characterization of adrenal pheochromocytoma using respiratory- triggered proton MR spectroscopy: initial experience. Wiseman GA, Pacak K, O'Dorisio MS, Neumann DR, Waxman AD, Mankoff DA, et al. Usefulness of 1. 23. I- MIBG scintigraphy in the evaluation of patients with known or suspected primary or metastatic pheochromocytoma or paraganglioma: results from a prospective multicenter trial. Fottner C, Helisch A, Anlauf M, Rossmann H, Musholt TJ, Kreft A, et al. F- fluoro- L- dihydroxyphenylalanine positron emission tomography is superior to 1. I- metaiodobenzyl- guanidine scintigraphy in the detection of extraadrenal and hereditary pheochromocytomas and paragangliomas: correlation with vesicular monoamine transporter expression. J Clin Endocrinol Metab. Jacobson AF, Deng H, Lombard J, Lessig HJ, Black RR. I- meta- iodobenzylguanidine scintigraphy for the detection of neuroblastoma and pheochromocytoma: results of a meta- analysis. J Clin Endocrinol Metab. Timmers HJ, Kozupa A, Chen CC, Carrasquillo JA, Ling A, Eisenhofer G, et al. Superiority of fluorodeoxyglucose positron emission tomography to other functional imaging techniques in the evaluation of metastatic SDHB- associated pheochromocytoma and paraganglioma. Luster M, Karges W, Zeich K, Pauls S, Verburg FA, Dralle H, et al. Clinical value of 1. F- fluorodihydroxyphenylalanine positron emission tomography/computed tomography (1. F- DOPA PET/CT) for detecting pheochromocytoma. Eur J Nucl Med Mol Imaging. Yamamoto S, Hellman P, Wassberg C, Sundin A. C- hydroxyephedrine positron emission tomography imaging of pheochromocytoma: a single center experience over 1. J Clin Endocrinol Metab. Preoperative preparation for pheochromocytoma resection: physician survey and clinical practice. Exp Clin Endocrinol Diabetes. Kwon SY, Lee KS, Lee JN, et al. Risk factors for hypertensive attack during pheochromocytoma resection. Identification of genes determining spontaneous hypertension. Hemodynamic instability during resection of pheochromocytoma in MEN versus non- MEN patients. Nau P, Demyttenaere S, Muscarella P, Narula V, Hazey JW, Ellison EC, et al. Pheochromocytoma does not increase risk in laparoscopic adrenalectomy. Laparoscopic adrenalectomy in pheochromocytoma: retroperitoneal approach versus transperitoneal approach. Scholten A, Valk GD, Ulfman D, Borel Rinkes IH, Vriens MR. Unilateral subtotal adrenalectomy for pheochromocytoma in multiple endocrine neoplasia type 2 patients: a feasible surgical strategy. Pheochromocytoma Crisis Is Not a Surgical Emergency. Medscape Medical News. Available at http: //www. Accessed: January 2. Scholten A, Cisco RM, Vriens MR, Cohen JK, Mitmaker EJ, Liu C, et al. Pheochromocytoma crisis is not a surgical emergency. J Clin Endocrinol Metab.
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