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 journalArticle

18 Citations (Scopus)
Original languageItalian
Pages (from-to)959-968
Number of pages10
JournalEndocrine
Volume55
Issue number3
DOIs
Publication statusPublished - 2017

Cite this

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 journalArticle

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.
@article{c46b95a0d1dc4dde9efc8d365609eba7,
title = "A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype",
author = "N.M. Albiger and D. Regazzo and B. Rubin and A.M. Ferrara and S. Rizzati and E. Taschin and F. Ceccato and G. Arnaldi and {Pecori Giraldi}, F. and A. Stigliano and L. Cerquetti and F. Grimaldi and {De Menis}, E. and M. Boscaro and M. Iacobone and G. Occhi and C. Scaroni",
note = "Cited By :3 Export Date: 7 February 2018",
year = "2017",
doi = "10.1007/s12020-016-0956-z",
language = "Italian",
volume = "55",
pages = "959--968",
journal = "Endocrine",
issn = "1355-008X",
publisher = "Humana Press Inc.",
number = "3",

}

TY - JOUR

T1 - A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

AU - Albiger, N.M.

AU - Regazzo, D.

AU - Rubin, B.

AU - Ferrara, A.M.

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.

N1 - Cited By :3 Export Date: 7 February 2018

PY - 2017

Y1 - 2017

U2 - 10.1007/s12020-016-0956-z

DO - 10.1007/s12020-016-0956-z

M3 - Articolo

VL - 55

SP - 959

EP - 968

JO - Endocrine

JF - Endocrine

SN - 1355-008X

IS - 3

ER -