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期刊名:Endocrine oncology

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e-ISSN:2634-4793

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共收录本刊相关文章索引137
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Stephen Gabriel Andrews,Steven D Forsythe,James P Madigan et al. Stephen Gabriel Andrews et al.
Small intestinal neuroendocrine tumors, siNETs, are a group of rare cancers that arise from neuroendocrine cells in the lining of the jejunum and ileum, which are either classified as tumors, siNETs, or small intestinal neuroendocrine carci...
Jino Johns Lalitha,Natarajan Ramalingam,Remya Rajan et al. Jino Johns Lalitha et al.
Objective: To analyse the risk factors of hypoparathyroidism and hypocalcaemia after total thyroidectomy. Methods: Clinical data of pat...
Anassuya Ramachandran,Polona Le Quesne Stabej,Veronica Boyle et al. Anassuya Ramachandran et al.
Although the gene MEN1 has a long-standing association with cancer, its mechanisms of action remain incompletely understood, acting both as a tumour suppressor in neuroendocrine tumours and as an oncogene in leukaemia. The best-characterise...
Emma Boehm,Terry Hung,Tim Akhurst et al. Emma Boehm et al.
Background: Metastatic gastroenteropancreatic neuroendocrine neoplasms (GEPNEN) can cause ectopic Cushing's syndrome (ECS). ECS is highly morbid and medical therapy is complex and can be ineffective. Patients unsuitable f...
Marcos Daniel Bortz,Andres Rodriguez,Maria Romina Luca et al. Marcos Daniel Bortz et al.
Objectives: We aim to investigate the time toxicity of patients with gastroenteropancreatic neuroendocrine tumours treated with Lutetium-177 Dotatate in a single institution. ...
Caitlin B Mauer Hall,Elise M Watson,Tanushree Prasad et al. Caitlin B Mauer Hall et al.
Background: Approximately 30-40% of paragangliomas (PGLs) and pheochromocytomas (PCCs) harbor an underlying hereditary cause. Early identification of at-risk individuals is imperative given the early onset, aggressiveness...
Carolina C Marques,Angelo B Brito,Eduardo N Lima et al. Carolina C Marques et al.
Background: 177-LuDOTATE is an effective but expensive treatment for neuroendocrine tumors (NETs). Reducing treatment-related costs, such as the number of images, could improve access to 177-LuDOTATE. We evaluated early r...
Elisa Lamback,Renan Lyra Miranda,Leila Chimelli et al. Elisa Lamback et al.
Pituitary gigantism is a rare pediatric disorder caused by excess growth hormone (GH) secretion. In almost 50% of cases, a genetic cause can be identified, with pathogenic variants in the aryl hydrocarbon receptor-interacting protein (AIP) ...
Patricia Gina Lu,Zhi Ven Fong,Patrick T Hangge et al. Patricia Gina Lu et al.
Background: The 2015 American Thyroid Association (ATA) guidelines added thyroid lobectomy (TL) as the appropriate treatment for low-risk differentiated thyroid cancer (DTC). We aimed to investigate the population-level f...
Yasuhiro Miki,Erina Iwabuchi,Chihiro Inoue et al. Yasuhiro Miki et al.
Elucidating the mechanisms of action of steroid hormones will contribute to the development of therapeutic strategies for hormone-dependent tumors. Recent advances in genetic engineering have revealed the complex and diverse mechanisms of s...