Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics(clinical),Oncology,Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10689-015-9818-8.pdf
Reference11 articles.
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2. Neumann HP, Pawlu C, Peczkowska M, Bausch B, McWhinney SR, Muresan M, Buchta M, Franke G, Klisch J, Bley TA, Hoegerle S, Boedeker CC, Opocher G, Schipper J, Januszewicz A, Eng C, European-American Paraganglioma Study Group (2004) Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA 292(8):943–951
3. Hashiba T, Maruno M, Fujimoto Y, Suzuki T, Wada K, Isaka T, Izumoto S, Yoshimine T (2006) Skull metastasis from papillary thyroid carcinoma accompanied by neurofibromatosis type 1 and pheochromocytoma: report of a case. Brain Tumor Pathol 23(2):97–100
4. Nasser T, Qari F (2009) Pheochromocytoma, papillary thyroid carcinoma. Saudi Med J 30(8):1087–1090
5. Huguet I, Walker L, Karavitaki N, Byrne J, Grossman AB (2013) Dandy-Walker malformation, papillary thyroid carcinoma, and SDHD-associated paraganglioma syndrome. J Clin Endocrinol Metab 98(12):4595–4596
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