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A CLINICAL OVERVIEW OF PHEOCHROMOCYTOMAS/PARAGANGLIOMAS AND CARCINOID TUMORS
Pheochromocytomas/paragangliomas are rare tumors, most are sporadic. Biochemical proof of disease is better with measurement of plasma metanephrines and less cumbersome than determinations in urine; its implementation is expanding. Anatomical imaging with computed tomography or magnetic resonance im...
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| Main Authors: | , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2008
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2597413/ https://ncbi.nlm.nih.gov/pubmed/18707631 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nucmedbio.2008.04.007 |
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