Arch. Endocrinol. Metab. 2017;61(5):414-415
Biochemical diagnosis of acromegaly without a typical clinical phenotype: what are the concerns?
DOI: 10.1590/2359-3997000000301
DOI: 10.1590/2359-3997000000301
Flow diagram of patient exclusion criteria for SNMTC and FNMTC groups.
Ribeiro-Oliveira Jr A, Barkan A. Biochemical diagnosis of acromegaly without a typical clinical phenotype: what are the concerns?. Arch. Endocrinol. Metab. 2017;61(5):414-5.
Ribeiro-Oliveira Jr, Antonio; Barkan, Ariel. Biochemical diagnosis of acromegaly without a typical clinical phenotype: what are the concerns?. Arch. Endocrinol. Metab., v. 61, n. 5, p. 414-415, Sep. 2017.
Ribeiro-Oliveira Jr, A., & Barkan, A. (2017). Biochemical diagnosis of acromegaly without a typical clinical phenotype: what are the concerns?. Arch. Endocrinol. Metab., 61(5), 414-415.
Ribeiro-Oliveira Jr, Antonio and Barkan, Ariel. Biochemical diagnosis of acromegaly without a typical clinical phenotype: what are the concerns?. Arch. Endocrinol. Metab. [online]. 2017, vol. 61, n. 5, [cited 2026-03-07], pp.414-415. Available from: <https://www.aem-sbem.com/article/biochemical-diagnosis-of-acromegaly-without-a-typical-clinical-phenotype-what-are-the-concerns/>. ISSN 2359-3997.