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Tyrosine kinase receptors as molecular targets In pheochromocytomas and paragangliomas

Pheochromocytomas and paragangliomas are neuroendocrine tumors shown to be responsive to multi-targeted tyrosine kinase inhibitor treatment. Despite growing knowledge regarding their genetic basis, the ability to predict behavior in these tumors remains challenging. There is also limited knowledge o...

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Detalles Bibliográficos
Publicado en:Mod Pathol
Main Authors: Cassol, Clarissa A., Winer, Daniel, Liu, Wei, Guo, Miao, Ezzat, Shereen, Asa, Sylvia L.
Formato: Artigo
Idioma:Inglês
Publicado: 2014
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4977182/
https://ncbi.nlm.nih.gov/pubmed/24390213
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/modpathol.2013.233
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