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Nature Reviews. Endocrinology|August 15, 2024
International consensus statement on the diagnosis and management of phaeochromocytoma and paraganglioma in children and adolescentsRuth T Casey, Emile Hendriks, Cheri Deal, et al.Theranostics|August 15, 2019
Integrative multi-omics analysis identifies a prognostic miRNA signature and a targetable miR-21-3p/TSC2/mTOR axis in metastatic pheochromocytoma/paragangliomaBruna Calsina, Luis Jaime Castro-Vega, Rafael Torres-Pérez, et al.European Journal of Endocrinology|November 9, 2020
ENSAT registry-based randomized clinical trials for adrenocortical carcinomaJoakim Crona, Eric Baudin, Massimo Terzolo, et al.Best Practice & Research. Clinical Endocrinology & Metabolism|September 1, 2024
MAML3-fusions modulate vascular and immune tumour microenvironment and confer high metastatic risk in pheochromocytoma and paragangliomaMaría Monteagudo, Bruna Calsina, Milton E Salazar-Hidalgo, et al.The Lancet. Diabetes & Endocrinology|July 27, 2020
Urine steroid metabolomics for the differential diagnosis of adrenal incidentalomas in the EURINE-ACT study: a prospective test validation studyIrina Bancos, Angela E Taylor, Vasileios Chortis, et al.The Lancet. Oncology|April 22, 2014
Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based studyFrederic Castinetti, Xiao-Ping Qi, Martin K Walz, et al.The Lancet. Diabetes & Endocrinology|January 21, 2019
Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective studyFrederic Castinetti, Steven G Waguespack, Andreas Machens, et al.Pageof 8