Martins Bugalho MJ - Search Results

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Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2.

Robinson MF, Furst EJ, Nunziata V, Brandi ML, Ferrer JP, Martins Bugalho MJ, di Giovanni G, Smith RJ, Donovan DT, Alford BR, et al. Robinson MF, et al. Among authors: martins bugalho mj. Henry Ford Hosp Med J. 1992;40(3-4):249-52. Henry Ford Hosp Med J. 1992. PMID: 1362415 Free article.

Clinical use of molecular information in the management of multiple endocrine neoplasia type 2A.

Gagel RF, Cote GJ, Martins Bugalho MJ, Boyd AE 3rd, Cummings T, Goepfert H, Evans DB, Cangir A, Khorana S, Schultz PN. Gagel RF, et al. Among authors: martins bugalho mj. J Intern Med. 1995 Oct;238(4):333-41. doi: 10.1111/j.1365-2796.1995.tb01207.x. J Intern Med. 1995. PMID: 7595169

Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literature.

Bancos I, Atkinson E, Eng C, Young WF Jr, Neumann HPH; International Pheochromocytoma and Pregnancy Study Group. Bancos I, et al. Lancet Diabetes Endocrinol. 2021 Jan;9(1):13-21. doi: 10.1016/S2213-8587(20)30363-6. Epub 2020 Nov 26. Lancet Diabetes Endocrinol. 2021. PMID: 33248478 Free PMC article.

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