A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

N.M. Albiger; D. Regazzo; B. Rubin; A.M. Ferrara; S. Rizzati; E. Taschin; F. Ceccato; G. Arnaldi; F. Pecori Giraldi; A. Stigliano; L. Cerquetti; F. Grimaldi; E. De Menis; M. Boscaro; M. Iacobone; G. Occhi; C. Scaroni

doi:10.1007/s12020-016-0956-z

A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

N.M. Albiger, D. Regazzo, B. Rubin, A.M. Ferrara, S. Rizzati, E. Taschin, F. Ceccato, G. Arnaldi, F. Pecori Giraldi, A. Stigliano, L. Cerquetti, F. Grimaldi, E. De Menis, M. Boscaro, M. Iacobone, G. Occhi, C. Scaroni

Research output: Contribution to journal › Article › peer-review

Original language	Italian
Pages (from-to)	959-968
Number of pages	10
Journal	Endocrine
Volume	55
Issue number	3
DOIs	https://doi.org/10.1007/s12020-016-0956-z
Publication status	Published - 2017

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10.1007/s12020-016-0956-z

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Albiger, N. M., Regazzo, D., Rubin, B., Ferrara, A. M., Rizzati, S., Taschin, E., Ceccato, F., Arnaldi, G., Pecori Giraldi, F., Stigliano, A., Cerquetti, L., Grimaldi, F., De Menis, E., Boscaro, M., Iacobone, M., Occhi, G., & Scaroni, C. (2017). A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype. Endocrine, 55(3), 959-968. https://doi.org/10.1007/s12020-016-0956-z

A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype. / Albiger, N.M.; Regazzo, D.; Rubin, B.; Ferrara, A.M.; Rizzati, S.; Taschin, E.; Ceccato, F.; Arnaldi, G.; Pecori Giraldi, F.; Stigliano, A.; Cerquetti, L.; Grimaldi, F.; De Menis, E.; Boscaro, M.; Iacobone, M.; Occhi, G.; Scaroni, C.

In: Endocrine, Vol. 55, No. 3, 2017, p. 959-968.

Research output: Contribution to journal › Article › peer-review

Albiger, NM, Regazzo, D, Rubin, B, Ferrara, AM, Rizzati, S, Taschin, E, Ceccato, F, Arnaldi, G, Pecori Giraldi, F, Stigliano, A, Cerquetti, L, Grimaldi, F, De Menis, E, Boscaro, M, Iacobone, M, Occhi, G & Scaroni, C 2017, 'A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype', Endocrine, vol. 55, no. 3, pp. 959-968. https://doi.org/10.1007/s12020-016-0956-z

Albiger, N.M. ; Regazzo, D. ; Rubin, B. ; Ferrara, A.M. ; Rizzati, S. ; Taschin, E. ; Ceccato, F. ; Arnaldi, G. ; Pecori Giraldi, F. ; Stigliano, A. ; Cerquetti, L. ; Grimaldi, F. ; De Menis, E. ; Boscaro, M. ; Iacobone, M. ; Occhi, G. ; Scaroni, C. / A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype. In: Endocrine. 2017 ; Vol. 55, No. 3. pp. 959-968.

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AU - Rizzati, S.

AU - Taschin, E.

AU - Ceccato, F.

AU - Arnaldi, G.

AU - Pecori Giraldi, F.

AU - Stigliano, A.

AU - Cerquetti, L.

AU - Grimaldi, F.

AU - De Menis, E.

AU - Boscaro, M.

AU - Iacobone, M.

AU - Occhi, G.

AU - Scaroni, C.

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