Metastatic MEN1 Syndrome Treated with Lutetium-177 – A Case Report

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant endocrine tumour syndrome characterised by three main manifestations: primary hyperparathyroidism (78–94%), gastroenteropancreatic neuroendocrine tumours (GEP-NETs) (35–78%) and pituitary adenomas (20–65%). For metastatic and inoper...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Eur Endocrinol
Asıl Yazarlar: Gezer, Emre, Çetinarslan, Berrin, Cantürk, Zeynep, Tarkun, İIlhan, Sözen, Mehmet, Selek, Alev
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Touch Medical Media 2019
Konular:
Endocrine Oncology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6785959/
https://ncbi.nlm.nih.gov/pubmed/31616499
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.17925/EE.2019.15.2.92
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