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La transizione del paziente con sindrome adreno-genitale da difetto di 21-idrossilasi

  • PRATICA CLINICA IN ENDOCRINOLOGIA
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Bibliografia

  1. Speiser PW, Arlt W, Auchus RJ et al. (2018) Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 103(11):4043–4088

    Article  Google Scholar 

  2. Bachelot A (2018) Transition of care from childhood to adulthood: congenital adrenal hyperplasia. Endocr Dev 33:17–33

    Article  Google Scholar 

  3. Merke DP, Poppas DP (2013) Management of adolescents with congenital adrenal hyperplasia. Lancet Diabetes Endocrinol 1(4):341–352

    Article  Google Scholar 

  4. Venneri MA, Hasenmajer V, Fiore D et al. (2018) Circadian rhythm of glucocorticoid administration entrains clock genes in immune cells: a DREAM Trial ancillary study. J Clin Endocrinol Metab 103(8):2998–3009

    Article  Google Scholar 

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Authors and Affiliations

  1. U.O.C. Endocrinologia, Dipartimento di Medicina-DIMED, Azienda Ospedaliera, Centro ENDO-ERN, Università degli Studi di Padova, Padova, Italia

    Mattia Barbot & Carla Scaroni

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  1. Mattia Barbot
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  2. Carla Scaroni
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Correspondence to Carla Scaroni.

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Gli autori Mattia Barbot e Carla Scaroni dichiarano di non avere conflitti di interesse.

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Barbot, M., Scaroni, C. La transizione del paziente con sindrome adreno-genitale da difetto di 21-idrossilasi. L'Endocrinologo 22, 564–566 (2021). https://doi.org/10.1007/s40619-021-00991-5

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  • DOI: https://doi.org/10.1007/s40619-021-00991-5

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