Paediatric phaeochromocytoma and paraganglioma: A clinical update.

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作者： Matthew A,Nazari ^[1] ; Abhishek,Jha ^[1] ; Mickey J M,Kuo ^[2] ; Mayank,Patel ^[1] ; Tamara,Prodanov ^[1] ; Jared S,Rosenblum ^[1] ; Sara,Talvacchio ^[1] ; Alberta,Derkyi ^[1] ; Kailah,Charles ^[1] ; Karel,Pacak ^[1]

作者单位： Developmental Endocrinology, Metabolism, Genetics and Endocrine Oncology Affinity Group, Section on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA. ^[1] Developmental Endocrinology, Metabolism, Genetics and Endocrine Oncology Affinity Group, Section on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.;Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA. ^[2]

关键词 disease management genetics molecular imaging paediatric paraganglioma pathology phaeochromocytoma

主题词儿童(Child);人类(Humans);肾上腺肿瘤(Adrenal Gland Neoplasms);副神经节瘤(Paraganglioma);嗜铬细胞瘤(Pheochromocytoma);预后(Prognosis)

DOI 10.1111/cen.14955

PMID 37515400

发布时间 2024-11-04

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准确一般字义偏差语意偏离译文作用小提交