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International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriers.
Amar L, Pacak K, Steichen O, Akker SA, Aylwin SJB, Baudin E, Buffet A, Burnichon N, Clifton-Bligh RJ, Dahia PLM, Fassnacht M, Grossman AB, Herman P, Hicks RJ, Januszewicz A, Jimenez C, Kunst HPM, Lewis D, Mannelli M, Naruse M, Robledo M, Taïeb D, Taylor DR, Timmers HJLM, Treglia G, Tufton N, Young WF, Lenders JWM, Gimenez-Roqueplo AP, Lussey-Lepoutre C. Amar L, et al. Among authors: lenders jwm. Nat Rev Endocrinol. 2021 Jul;17(7):435-444. doi: 10.1038/s41574-021-00492-3. Epub 2021 May 21. Nat Rev Endocrinol. 2021. PMID: 34021277 Free PMC article. Review.
Biochemical diagnosis of pheochromocytoma: which test is best?
Lenders JW, Pacak K, Walther MM, Linehan WM, Mannelli M, Friberg P, Keiser HR, Goldstein DS, Eisenhofer G. Lenders JW, et al. JAMA. 2002 Mar 20;287(11):1427-34. doi: 10.1001/jama.287.11.1427. JAMA. 2002. PMID: 11903030
Pheochromocytoma as an endocrine emergency.
Brouwers FM, Lenders JW, Eisenhofer G, Pacak K. Brouwers FM, et al. Rev Endocr Metab Disord. 2003 May;4(2):121-8. doi: 10.1023/a:1022981801344. Rev Endocr Metab Disord. 2003. PMID: 12766539 Review. No abstract available.
251 results