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3. Mutations of the metabolic genes IDH1, IDH2, and SDHAF2 are not major determinants of the pseudohypoxic phenotype of sporadic pheochromocytomas and paragangliomas. Yao L; Barontini M; Niederle B; Jech M; Pfragner R; Dahia PL J Clin Endocrinol Metab; 2010 Mar; 95(3):1469-72. PubMed ID: 20130071 [TBL] [Abstract][Full Text] [Related]
4. An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. van Nederveen FH; Gaal J; Favier J; Korpershoek E; Oldenburg RA; de Bruyn EM; Sleddens HF; Derkx P; Rivière J; Dannenberg H; Petri BJ; Komminoth P; Pacak K; Hop WC; Pollard PJ; Mannelli M; Bayley JP; Perren A; Niemann S; Verhofstad AA; de Bruïne AP; Maher ER; Tissier F; Méatchi T; Badoual C; Bertherat J; Amar L; Alataki D; Van Marck E; Ferrau F; François J; de Herder WW; Peeters MP; van Linge A; Lenders JW; Gimenez-Roqueplo AP; de Krijger RR; Dinjens WN Lancet Oncol; 2009 Aug; 10(8):764-71. PubMed ID: 19576851 [TBL] [Abstract][Full Text] [Related]
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18. 15 YEARS OF PARAGANGLIOMA: Genetics and mechanism of pheochromocytoma-paraganglioma syndromes characterized by germline SDHB and SDHD mutations. Baysal BE; Maher ER Endocr Relat Cancer; 2015 Aug; 22(4):T71-82. PubMed ID: 26113606 [TBL] [Abstract][Full Text] [Related]
19. Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes? Jiménez C; Cote G; Arnold A; Gagel RF J Clin Endocrinol Metab; 2006 Aug; 91(8):2851-8. PubMed ID: 16735498 [TBL] [Abstract][Full Text] [Related]