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Cited by in F6Publishing
For: Chen X, Hu L, Liu C, Ni G, Zhang Y. Tumor characteristics and surgical outcome in incidentally discovered pheochromocytomas and paragangliomas. Endocr Connect 2018:/journals/ec/aop/ec-18-0268. [PMID: 30352413 DOI: 10.1530/EC-18-0268] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
Number Citing Articles
1 Uslar T, San Francisco IF, Olmos R, Macchiavelo S, Zuñiga A, Rojas P, Garrido M, Huete A, Mendez GP, Cortinez I, Zemelman JT, Cifuentes J, Castro F, Olivari D, Domínguez JM, Arteaga E, Fardella CE, Valdés G, Tagle R, Baudrand R. Clinical Presentation and Perioperative Management of Pheochromocytomas and Paragangliomas: A 4-Decade Experience. J Endocr Soc 2021;5:bvab073. [PMID: 34377881 DOI: 10.1210/jendso/bvab073] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
2 Choi H, Kim KJ, Hong N, Shin S, Choi JR, Kang SW, Lee ST, Rhee Y. Genetic Analysis and Clinical Characteristics of Hereditary Pheochromocytoma and Paraganglioma Syndrome in Korean Population. Endocrinol Metab (Seoul) 2020;35:858-72. [PMID: 33397040 DOI: 10.3803/EnM.2020.683] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]