A COVID-19 pneumonia case report of autoimmune polyendocrine syndrome type 1 in Lombardy, Italy: letter to the editor
Beccuti, G., Ghizzoni, L., Cambria, V., Codullo, V., Sacchi, P., Lovati, E., Mongodi, S., Iotti, G. A., Mojoli, F.
Published in Journal of endocrinological investigation (01.08.2020)
Published in Journal of endocrinological investigation (01.08.2020)
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POR polymorphisms are associated with 21 hydroxylase deficiency
Pecori Giraldi, F., Einaudi, S., Sesta, A., Verna, F., Messina, M., Manieri, C., Menegatti, E., Ghizzoni, L.
Published in Journal of endocrinological investigation (01.10.2021)
Published in Journal of endocrinological investigation (01.10.2021)
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Multicenter retro-prospective observational study on chronic hypoparathyroidism and rhPTH (1–84) treatment
Marcucci, G., Beccuti, G., Carosi, G., Cetani, F., Cianferotti, L., Colao, A. M., Di Somma, C., Duradoni, M., Elefante, A., Ghizzoni, L., Giusti, M., Lania, A. G., Lavezzi, E., Madeo, B., Mantovani, G., Marcocci, C., Masi, L., Parri, S., Pigliaru, F., Santonati, A., Spada, A., Vera, L., Brandi, M. L.
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Published in Journal of endocrinological investigation (01.09.2022)
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Evidence for Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias
Vottero, A, Minari, R, Viani, I, Tassi, F, Bonatti, F, Neri, T. M, Bertolini, L, Bernasconi, S, Ghizzoni, L
Published in The journal of clinical endocrinology and metabolism (01.12.2011)
Published in The journal of clinical endocrinology and metabolism (01.12.2011)
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Tryptophan Hydroxylase Autoantibodies as Markers of a Distinct Autoimmune Gastrointestinal Component of Autoimmune Polyendocrine Syndrome Type 1
Scarpa, R, Alaggio, R, Norberto, L, Furmaniak, J, Chen, S, Smith, B. Rees, Masiero, S, Morlin, L, Plebani, M, De Luca, F, Salerno, M. C, Giordano, R, Radetti, G, Ghizzoni, L, Tonini, G, Farinati, F, Betterle, C
Published in The journal of clinical endocrinology and metabolism (01.02.2013)
Published in The journal of clinical endocrinology and metabolism (01.02.2013)
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Effectiveness of a prevention program for diabetic ketoacidosis in children. An 8-year study in schools and private practices
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Published in Diabetes care (01.01.1999)
Published in Diabetes care (01.01.1999)
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Functional and structural analysis of four novel mutations of CYP21A2 gene in Italian patients with 21-hydroxylase deficiency
Massimi, A, Malaponti, M, Federici, L, Vinciguerra, D, Manca Bitti, M L, Vottero, A, Ghizzoni, L, Maccarrone, M, Cappa, M, Bernardini, S, Porzio, O
Published in Hormone and metabolic research (01.06.2014)
Published in Hormone and metabolic research (01.06.2014)
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Autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy in Calabria: Clinical, immunological and genetic patterns
Betterle, C., Ghizzoni, L., Cassio, A., Baronio, F., Cervato, S., Garelli, S., Barbi, E., Tonini, G.
Published in Journal of endocrinological investigation (01.11.2012)
Published in Journal of endocrinological investigation (01.11.2012)
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Decreased Androgen Receptor Gene Methylation in Premature Pubarche: A Novel Pathogenetic Mechanism?
Vottero, A, Capelletti, M, Giuliodori, S, Viani, I, Ziveri, M, Neri, T. M, Bernasconi, S, Ghizzoni, L
Published in The journal of clinical endocrinology and metabolism (01.03.2006)
Published in The journal of clinical endocrinology and metabolism (01.03.2006)
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Leptin inhibits steroid biosynthesis by human granulosa-lutein cells
Ghizzoni, L, Barreca, A, Mastorakos, G, Furlini, M, Vottero, A, Ferrari, B, Chrousos, G P, Bernasconi, S
Published in Hormone and metabolic research (01.06.2001)
Published in Hormone and metabolic research (01.06.2001)
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Long-term auxological and pubertal outcome of patients with hereditary insulin-like growth factor-I deficiency (Laron and growth hormone-gene deletion syndrome) treated with recombinant human insulin-like growth factor-I
Messina, M. F., Arrigo, T., Valenzise, M., Ghizzoni, L., Caruso-Nicoletti, M., Zucchini, S., Chiabotto, P., Crisafulli, G., Zirilli, G., De Luca, F.
Published in Journal of endocrinological investigation (01.04.2011)
Published in Journal of endocrinological investigation (01.04.2011)
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Journal Article
Long-term auxological and pubertal outcome of patients with hereditary insulin-like growth factor-I deficiency (Laron and growth hormone-gene deletion syndrome) treated with recombinant human insulin-like growth factor-I
Messina, M F, Arrigo, T, Valenzise, M, Ghizzoni, L, Caruso-Nicoletti, M, Zucchini, S, Chiabotto, P, Crisafulli, G, Zirilli, G, De Luca, F
Published in Journal of endocrinological investigation (01.04.2011)
Published in Journal of endocrinological investigation (01.04.2011)
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Foreword. Ferring-sponsored International Symposia on Paediatric Endocrinology
Chiarelli, F, Delemarre-van de Waal, H, Ghizzoni, L, Hughes, I
Published in European journal of endocrinology (01.12.2008)
Published in European journal of endocrinology (01.12.2008)
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GH secretion in a cohort of children with pseudohypoparathyroidism type Ia
de Sanctis, L, Bellone, J, Salerno, M, Faleschini, E, Caruso-Nicoletti, M, Cicchetti, M, Concolino, D, Balsamo, A, Buzi, F, Ghizzoni, L, de Sanctis, C
Published in Journal of endocrinological investigation (01.02.2007)
Published in Journal of endocrinological investigation (01.02.2007)
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Precocious puberty in girls adopted from developing countries
Virdis, Raffaele, Street, Maria E, Zampolli, Maria, Radetti, Giorgio, Pezzini, Barbara, Benelli, Marzia, Ghizzoni, Lucia, Volta, Cecilia
Published in Archives of disease in childhood (01.02.1998)
Published in Archives of disease in childhood (01.02.1998)
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Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1
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Published in The Journal of experimental medicine (05.07.2021)
Published in The Journal of experimental medicine (05.07.2021)
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Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
Speiser, Phyllis W, Azziz, Ricardo, Baskin, Laurence S, Ghizzoni, Lucia, Hensle, Terry W, Merke, Deborah P, Meyer-Bahlburg, Heino F. L, Miller, Walter L, Montori, Victor M, Oberfield, Sharon E, Ritzen, Martin, White, Perrin C
Published in The journal of clinical endocrinology and metabolism (01.09.2010)
Published in The journal of clinical endocrinology and metabolism (01.09.2010)
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Evaluation of the circadian profile of peripheral plasma galanin concentrations in normal subjects
Ceresini, G, Morganti, S, Rebecchi, I, Solerte, S.B, Ghizzoni, L, Ablondi, F, Valenti, G
Published in Life sciences (1973) (19.04.2002)
Published in Life sciences (1973) (19.04.2002)
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Journal Article
Corrigendum to: “Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline”
Speiser, PW, Azziz, R, Baskin, LS, Ghizzoni, L, Hensle, TW, Merke, DP, Meyer-Bahlburg, HFL, Miller, WL, Montori, VM, Oberfield, SE, Ritzen, M, White, PC
Published in The journal of clinical endocrinology and metabolism (01.07.2021)
Published in The journal of clinical endocrinology and metabolism (01.07.2021)
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