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Case Report of a Prolactinoma in a Patient With a Novel MAX Mutation and Bilateral Pheochromocytomas
Pheochromocytomas are neuroendocrine tumors that can arise sporadically or be inherited as a familial disease, and they may occur in isolation or as part of a multitumor syndrome. Familial disease typically presents in younger patients with a higher risk of multifocality. Recently, the tumor suppres...
Autores principales: | Roszko, Kelly Lauter, Blouch, Erica, Blake, Michael, Powers, James F., Tischler, Arthur S., Hodin, Richard, Sadow, Peter, Lawson, Elizabeth A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Endocrine Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686672/ https://www.ncbi.nlm.nih.gov/pubmed/29264463 http://dx.doi.org/10.1210/js.2017-00135 |
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