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Update of Pheochromocytoma Syndromes: Genetics, Biochemical Evaluation, and Imaging
Pheochromocytomas and paragangliomas (PCCs/PGLs) are rare commonly benign neuroendocrine tumors that share pathology features and clinical behavior in many cases. While PCCs are chromaffin-derived tumors that arise within the adrenal medulla, PGLs are neural-crest-derived tumors that originate at th...
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| Publicado en: | Front Endocrinol (Lausanne) |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2018
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6277481/ https://ncbi.nlm.nih.gov/pubmed/30538672 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2018.00515 |
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