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Endocrinologia Clínica (Lúcio Vilar) - 6 Edição_Parte231

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Buchfelder M. Management of aggressive pituitary adenomas: current treatment strategies. Pituitary. 2009; 12:256-60.
Kaltsas GA, Nomikos P, Kontogeorgos G et al. Clinical review: diagnosis and management of pituitary carcinomas. J Clin
Endocrinol Metab. 2005; 90:3089-99.
Chatzellis E, Alexandraki KI, Androulakis II et al. Aggressive pituitary tumors. Neuroendocrinology. 2015; 101:87-104.
Alimohamadi M, Ownagh V, Mahouzi L et al. The impact of immunohistochemical markers of Ki-67 and p53 on the long-
term outcome of growth hormone-secreting pituitary adenomas: a cohort study. Asian J Neurosurg. 2014; 9:130-6.
Ruebel KH, Leontovich AA, Jin L et al. Patterns of gene expression in pituitary carcinomas and adenomas analyzed by
high-density oligonucleotide arrays, reverse transcriptase-quantitative PCR, and protein expression. Endocr J. 2006;
29:435-44.
Wierinckx A, Auger C, Devauchelle P et al. A diagnostic marker set for invasion, proliferation, and aggressiveness of
prolactin pituitary tumors. Endocr Relat Cancer. 2007; 14:887-900.
Mete O, Ezzat S, Asa SL. Biomarkers of aggressive pituitary adenomas. J Mol Endocrinol. 2012; 49:R69-78.
Kawashima ST, Usui T, Sano T et al. P53 gene mutation in an atypical corticotroph adenoma with Cushing’s disease. Clin
Endocrinol (Oxf). 2009; 70:656-7.
Tfelt-Hansen J, Kunparthi D, Chattopadhyay N. The emerging role of pituitary tumor transforming gene in tumorigenesis.
Clin Med Res. 2006; 4:130-7.
Xiao JQ, Liu XH, Hou B et al. Correlations of pituitary tumor transforming gene expression with human pituitary
adenomas: a meta-analysis. PLoS One. 2014; 9:e90396.
Li Y, Zhou LP, Ma P et al. Relationship of PTTG expression with tumor invasiveness and microvessel density of pituitary
adenomas: a meta-analysis. Genet Test Mol Biomarkers. 2014; 18:279-85.
Filippella M, Galland F, Kujas M et al. Pituitary tumour transforming gene (PTTG) expression correlates with the
proliferative activity and recurrence status of pituitary adenomas: a clinical and immunohistochemical study. Clin
Endocrinol (Oxf). 2006; 65:536-43.
Delgrange E, Trouillas J, Maiter D et al. Sex-related difference in the growth of prolactinomas: a clinical and proliferation
marker study. J Clin Endocrinol Metab. 1997; 82:2102-7.
Hardy J. Transphenoidal microsurgery of the normal and pathological pituitary. Clin Neurosurg. 1969; 16:185-217.
Chiloiro S, Doglietto F, Trapasso B et al. Typical and atypical pituitary adenomas: a single-center analysis of outcome and
prognosis. Neuroendocrinology. 2015; 101:143-50.
Rotondo F, Cusimano M, Scheithauer BW et al. Atypical, invasive, recurring Crooke cell adenoma of the pituitary.
Hormones (Athens). 2012; 11:94-100.
Heaney A. Management of aggressive pituitary adenomas and pituitary carcinomas. J Neuro-oncol. 2014; 117:459-68.
Maiter D, Delgrange E. Therapy of endocrine disease: the challenges in managing giant prolactinomas. Eur J Endocrinol.
2014; 170:R213-27.
Zornitzki T, Knobler H, Nass D et al. Increased MIB-1/Ki-67 labeling index as a predictor of an aggressive course in a case
of prolactinoma. Horm Res. 2004; 61:111-6.
Molitch ME. Management of medically refractory prolactinoma. J Neuro-oncol. 2014; 117:421-8.
Mercado M, Espinosa E, Ramírez C. Current status and future directions of the pharmacological therapy of acromegaly.
Minerva Endocrinol. 2015 Oct 20. [Epub ahead of print.]
Espinosa-de-los-Monteros AL, Gonzalez B, Vargas G et al. Octreotide LAR treatment of acromegaly in “real life”: long-
term outcome at a tertiary care center. Pituitary. 2015; 18:290-6.
 Ramos-Leví AM, Bernabeu I, Álvarez-Escolá C et al. Long-term treatment with pegvisomant for acromegaly: a 10-year
experience. Clin Endocrinol (Oxf). 2015. [Epub ahead of print.]
Hofland LJ, van der Hoek J, Feelders R et al. The multiligand somatostatina analogue SOM230 inhibits ACTH secretion by
cultured human corticotroph adenomas via somatostatin receptor type 5. Eur J Endocrinol. 2005; 152:645-54.
Cuevas-Ramos D, Fleseriu M. Treatment of Cushing’s disease: a mechanistic update. J Endocrinol. 2014; 223:R19-39.
Simeoli C, Auriemma RS, Tortora F et al. The treatment with pasireotide in Cushing’s disease: effects of long-term
treatment on tumor mass in the experience of a single center. Endocrine. 2015; 50:725-40.
Vilar L, Naves LA, Machado MC et al. Medical combination therapies in Cushing’s disease. Pituitary. 2015; 18:253-62.
Hart MG, Garside R, Rogers G et al. Temozolomide for high grade glioma. Cochrane Database Syst Rev.
2013;4:CD007415.
Pietrantonio F, Perrone F, De Braud F et al. Activity of temozolomide in patients with advanced chemorefractory colorectal
cancer and MGMT promoter methylation. Ann Oncol. 2014;25:404-8.
Quirt I, Verma S, Petrella T et al. Temozolomide for the treatment of metastatic melanoma: a systematic review. Oncologist.
2007;12:1114-23.
	Endocrinologia Clínica (Lúcio Vilar) - 6ª Edição

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