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Central Precocious Puberty in Italian Boys: Data From a Large Nationwide Cohort.
Cassio A, Marescotti G, Aversa T, Salerno M, Tornese G, Stancampiano M, Tuli G, Faienza MF, Cavarzere P, Fava D, Parpagnoli M, Bruzzi P, Ibba A, Calcaterra V, Mameli C, Grandone A, Cherubini V, Assirelli V, Franchina F, Capalbo D, Mase RD, Tamaro G, Cavasin J, Munarin J, Russo G, Wasniewska M; Physiopathology of Growth Processes and Puberty Study Group of the Italian Society for Pediatric Endocrinology and Diabetology. Cassio A, et al. Among authors: ibba a. J Clin Endocrinol Metab. 2024 Feb 3:dgae035. doi: 10.1210/clinem/dgae035. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38308814
Diagnosis of GH Deficiency Without GH Stimulation Tests.
Ibba A, Loche S. Ibba A, et al. Front Endocrinol (Lausanne). 2022 Feb 18;13:853290. doi: 10.3389/fendo.2022.853290. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35250894 Free PMC article. Review.
Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study.
Tromp TR, Hartgers ML, Hovingh GK, Vallejo-Vaz AJ, Ray KK, Soran H, Freiberger T, Bertolini S, Harada-Shiba M, Blom DJ, Raal FJ, Cuchel M; Homozygous Familial Hypercholesterolaemia International Clinical Collaborators. Tromp TR, et al. Lancet. 2022 Feb 19;399(10326):719-728. doi: 10.1016/S0140-6736(21)02001-8. Epub 2022 Jan 28. Lancet. 2022. PMID: 35101175 Free PMC article.
Craniocervical abnormalities in osteogenesis imperfecta type V.
Ludwig K, Seiltgens C, Ibba A, Saran N, Ouellet JA, Glorieux F, Rauch F. Ludwig K, et al. Among authors: ibba a. Osteoporos Int. 2022 Jan;33(1):177-183. doi: 10.1007/s00198-021-06088-x. Epub 2021 Aug 5. Osteoporos Int. 2022. PMID: 34350492
64 results