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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:Clin Cancer Res
Glavni autori: 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.
Format: Artigo
Jezik:Inglês
Izdano: 2017
Teme:
Article
Online pristup: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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items