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A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype.
Palumbo S, Cirillo G, Sanchez G, Aiello F, Fachin A, Baldo F, Pellegrin MC, Cassio A, Salerno M, Maghnie M, Faienza MF, Wasniewska M, Fintini D, Giacomozzi C, Ciccone S, Miraglia Del Giudice E, Tornese G, Grandone A. Palumbo S, et al. Among authors: grandone a. J Endocrinol Invest. 2023 Jun;46(6):1233-1240. doi: 10.1007/s40618-022-01997-y. Epub 2022 Dec 28. J Endocrinol Invest. 2023. PMID: 36577869
A case of Rubinstein-Taybi syndrome associated with growth hormone deficiency in childhood.
Tornese G, Marzuillo P, Pellegrin MC, Germani C, Faleschini E, Zennaro F, Grandone A, Miraglia del Giudice E, Perrone L, Ventura A. Tornese G, et al. Among authors: grandone a. Clin Endocrinol (Oxf). 2015 Sep;83(3):437-9. doi: 10.1111/cen.12748. Epub 2015 Mar 6. Clin Endocrinol (Oxf). 2015. PMID: 25683362 No abstract available.
115 results