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Pheochromocytomas and Paragangliomas: From Genetic Diversity to Targeted Therapies
Pheochromocytoma and paraganglioma (PCPGs) are rare neuroendocrine tumors that arise from the chromaffin tissue of adrenal medulla and sympathetic ganglia. Although metastatic PCPGs account for only 10% of clinical cases, morbidity and mortality are high because of the uncontrollable mass effect and...
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| Publicado no: | Cancers (Basel) |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6521122/ https://ncbi.nlm.nih.gov/pubmed/30925729 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cancers11040436 |
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