SDHB-Associated Paraganglioma in a Pediatric Patient and Literature Review on Hereditary Pheochromocytoma-Paraganglioma Syndromes.
Choat H, Derrevere K, Knight L, Brown W, Mack EH.
Case Rep Endocrinol. 2014;2014:502734. doi: 10.1155/2014/502734. Epub 2014 Sep 15.
PMID:25298897
Hereditary hormone excess: genes, molecular pathways, and syndromes.
Marx SJ, Simonds WF.
Endocr Rev. 2005 Aug;26(5):615-61. doi: 10.1210/er.2003-0037. Epub 2005 Jan 4.
PMID:15632315
[Diagnostic problems in pheochromocytoma].
Mannelli M, Pupilli C, Lanzillotti R, Ianni L, Bellini F.
Minerva Endocrinol. 1995 Mar;20(1):55-61.
PMID:7651283
[(18)F]SiTATE-PET/CT for detection of pheochromocytomas and paragangliomas: comparison of biochemical secretion, genotype and imaging metrics.
Onkes M, Dahlmann P, Gesenhues A, Gacula SIG, Mansour N, Schweizer JROL, Stüfchen I, Lottspeich C, Wang K, Auer MK, Brendel M, Fischer A, Braunschweig T, Gildehaus FJ, Lindner S, Schmid-Tannwald C, Pfluger T, Auernhammer CJ, Nölting S, Werner RA, Reincke M, Bidlingmaier M, Kroiss M, Völter F.
Eur J Nucl Med Mol Imaging. 2025 May 30. doi: 10.1007/s00259-025-07341-9. Online ahead of print.
PMID:40445313
Neuroendocrine secretory protein-55 (NESP-55) expression discriminates pancreatic endocrine tumors and pheochromocytomas from gastrointestinal and pulmonary carcinoids.
Srivastava A, Padilla O, Fischer-Colbrie R, Tischler AS, Dayal Y.
Am J Surg Pathol. 2004 Oct;28(10):1371-8. doi: 10.1097/01.pas.0000135527.96318.20.
PMID:15371954
Metabolome profiling by HRMAS NMR spectroscopy of pheochromocytomas and paragangliomas detects SDH deficiency: clinical and pathophysiological implications.
Imperiale A, Moussallieh FM, Roche P, Battini S, Cicek AE, Sebag F, Brunaud L, Barlier A, Elbayed K, Loundou A, Bachellier P, Goichot B, Stratakis CA, Pacak K, Namer IJ, Taïeb D.