Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: clinical features, genetics and surveillance recommendations in childhood

Children and adolescents who present with neuroendocrine tumors are at extremely high likelihood of having an underlying germline predisposition for the Multiple Endocrine Neoplasia (MEN) syndromes, including MEN1, MEN2A and B, MEN4, and Hyperparathyroid-Jaw Tumor (HPT-JT) Syndromes. Each of these a...

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Bibliografiset tiedot
Julkaisussa:Clin Cancer Res
Päätekijät: Wasserman, Jonathan D., Tomlinson, Gail E., Druker, Harriet, Kamihara, Junne, Kohlmann, Wendy K., Kratz, Christian P., Nathanson, Katherine L., Pajtler, Kristian W., Parareda, Andreu, Rednam, Surya P., States, Lisa J., Villani, Anita, Walsh, Michael F., Zelley, Kristin, Schiffman, Joshua D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2017
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5547889/
https://ncbi.nlm.nih.gov/pubmed/28674121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1078-0432.CCR-17-0548
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