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Endocrinol (Oxf). 2006; 65:699-705.
Lenders JW, Duh QY, Eisenhofer G et al. Pheochromocytoma and para-ganglioma: an Endocrine Society clinical practice
guideline. J Clin Endocrinol Metab. 2014; 99:1915-42.
Karasek D, Shad U, Frysak Z et al. An update on the genetics of pheochromocytoma. J Hum Hypertens. 2013; 27:141-7.
Toledo RA, Qin Y, Cheng ZM et al. Recurrent mutations of chromatinremodeling genes and kinase receptors in
pheochromocytomas and para-gangliomas. Clin Cancer Res. 2016; 22:2301-10.
Bouloux PMG, Fakeeh M. Investigation of pheocromocytoma. Clin Endocrinol (Oxf). 1995; 43:657-64.
Pappachan JM, Raskauskiene D, Sriraman R et al. Diagnosis and management of pheochromocytoma: a practical guide to
clinicians. Curr Hypertens Rep. 2014; 16:442.
Grossman A, Pacak K, Sawka A et al. Biochemical diagnosis and localization of pheochromocytoma: can we reach a
consensus? Ann N Y Acad Sci. 2006; 1073:332-47.
 Young WF Jr. Endocrine hypertension. In: Melmed S, Polonsky KS, Larsen PR et al. (Ed.). Williams textbook of
endocrinology. 12. ed. Philadelphia: Elsevier Saunders, 2011. p. 545-77.
Fitzgerald PA. Adrenal medulla and paraganglia. In: Gardner DG, Shoback D (Ed.). Greenspan’s basic & clinical
endocrinology. 9. ed. New York: McGraw Hill Co, 2011. p. 345-93.
O’Riordan DS, Young WF Jr, Grant CS et al. Clinical spectrum and outcome of functional extra-adrenal paraganglioma.
World J Surg. 1996; 20:916-21.
Sambaziotis D, Kontogeorgos G, Kovacs K et al. Intrasellar paraganglioma presenting as nonfunctioning pituitary adenoma.
Arch Pathol Lab Med. 1999; 123:429-32.
Wilhelm SM, Prinz RA, Barbu AM et al. Analysis of large versus small pheochromocytomas: operative approaches and
patient outcomes. Surgery. 2006; 140:553-9; discussion 559-60.
Shen WT, Sturgeon C, Clark OH et al. Should pheochromocytoma size influence surgical approach? A comparison of 90
malignant and 60 benign pheochromocytomas. Surgery. 2004; 136:1129-37.
Ahlman H. Malignant phaeochromocytoma. State of the field with future projections. Ann N Y Acad Sci. 2006; 1073:449-
64.
Richard S, Graff J, Lindau J et al. Von Hippel-Lindau disease. Lancet. 2004; 363:1231-4.
Maher ER, Neumann HP, Richard S. Von Hippel-Lindau disease: a clinical and scientific review. Eur J Hum Genet. 2011;
19:617-23.
Barontini M, Dahia PL. VHL disease. Best Pract Res Clin Endocrinol Metab. 2010; 24:401-13.
Tischler AS. Pheochromocytoma and extra-adrenal paraganglioma: updates. Arch Pathol Lab Med. 2008; 132:1272-84.
Boedeker CC, Erlic Z, Richard S et al. Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine
neoplasia type 2. J Clin Endocrinol Metab. 2009; 94:1938-44.
Gimenez-Roqueplo AP, Dahia PL, Robledo M. An update on the genetics of paraganglioma, pheochromocytoma, and
associated hereditary syndromes. Horm Metab Res. 2012; 44:328-33.
Erem C, Onder Ersöz H, Ukinç K et al. Neurofibromatosis type 1 associated with pheochromocytoma: a case report and a
review of the literature. J Endocrinol Invest. 2007; 30:59-64.
Herrera RN, Miotti JA, Fuentes CM et al. Pheochromocytoma associated with von Recklinghausen neurofibromatosis.
Medicina (B Aires). 2007; 67:475-7.
Moline J, Eng C. Multiple endocrine neoplasia type 2: an overview. Genet Med. 2011; 13:755-64.
Qin Y, Yao L, King EE et al. Germline mutations in TMEM127 confer susceptibility to pheochromocytoma. Nat Genet.
2010; 42:229-33.
Abermil N, Guillaud-Bataille M, Burnichon N et al. TMEM127 Screening in a large cohort of patients with
pheochromocytoma and/or paraganglioma. J Clin Endocrinol Metab. 2012; 97:E805-9.
Brenner N, Kopetschke R, Ventz M et al. Cushing’s syndrome due to ACTH-secreting pheochromocytoma. Can J Urol.
2008; 15:3924-7.
Canda AE, Sis B, Sokmen S et al. An unusual mesenteric paraganglioma producing human chorionic gonadotropin. Tumori.
2004; 90:249-52.
Mandel M, Saad F, Andrade FG et al. Paraganglioma produtor de prolactina: relato de dois casos. Arq Bras Endocrinol
Metab. 2003; 47(Suppl 1):S322.
Thomas JE, Rook ED, Kvale WF. The neurologist’s experience with pheochromocytoma: a review of 46 cases. J Urol.
1974; 111:715-21.
Rosas AL, Kasperlik-Zaluska AA, Papierska L et al. Pheochromocytoma crisis induced by glucocorticoids: a report of four
cases and review of the literature. Eur J Endocrinol. 2008; 158:423-9.
Olson SW, Deal LE, Piesman M. Epinephrine-secreting pheochromocytoma presenting with cardiogenic shock and
	Endocrinologia Clinica - Vilar 6 edicao

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