Baroncelli GI - Search Results

1

Complete Androgen Insensitivity Syndrome: From Bench to Bed.

Tyutyusheva N, Mancini I, Baroncelli GI, D'Elios S, Peroni D, Meriggiola MC, Bertelloni S. Tyutyusheva N, et al. Among authors: baroncelli gi. Int J Mol Sci. 2021 Jan 27;22(3):1264. doi: 10.3390/ijms22031264. Int J Mol Sci. 2021. PMID: 33514065 Free PMC article. Review.

2

Puberty and bone development.

Saggese G, Baroncelli GI, Bertelloni S. Saggese G, et al. Among authors: baroncelli gi. Best Pract Res Clin Endocrinol Metab. 2002 Mar;16(1):53-64. doi: 10.1053/beem.2001.0180. Best Pract Res Clin Endocrinol Metab. 2002. PMID: 11987898 Review.

3

Lumbar bone mineral density at final height and prevalence of fractures in treated children with GH deficiency.

Baroncelli GI, Bertelloni S, Sodini F, Saggese G. Baroncelli GI, et al. J Clin Endocrinol Metab. 2002 Aug;87(8):3624-31. doi: 10.1210/jcem.87.8.8754. J Clin Endocrinol Metab. 2002. PMID: 12161486

4

Growth and puberty in Turner's syndrome.

Bertelloni S, Baroncelli GI, Fruzzetti F, Spinelli C, Simi P, Saggese G. Bertelloni S, et al. Among authors: baroncelli gi. J Pediatr Endocrinol Metab. 2003 Mar;16 Suppl 2:307-15. J Pediatr Endocrinol Metab. 2003. PMID: 12729409 Review.

5

Acquisition of bone mass in normal individuals and in patients with growth hormone deficiency.

Baroncelli GI, Bertelloni S, Sodini F, Saggese G. Baroncelli GI, et al. J Pediatr Endocrinol Metab. 2003 Mar;16 Suppl 2:327-35. J Pediatr Endocrinol Metab. 2003. PMID: 12729412 Review.

6

Longitudinal changes of lumbar bone mineral density (BMD) in patients with GH deficiency after discontinuation of treatment at final height; timing and peak values for lumbar BMD.

Baroncelli GI, Bertelloni S, Sodini F, Saggese G. Baroncelli GI, et al. Clin Endocrinol (Oxf). 2004 Feb;60(2):175-84. doi: 10.1046/j.1365-2265.2003.01949.x. Clin Endocrinol (Oxf). 2004. PMID: 14725678

7

Cortical bone density is normal in prepubertal children with growth hormone (GH) deficiency, but initially decreases during gh replacement due to early bone remodeling.

Baroncelli GI, Bertelloni S, Galli L, Sodini F, Saggese G. Baroncelli GI, et al. J Clin Endocrinol Metab. 2004 May;89(5):2505; author reply 2505-6. doi: 10.1210/jc.2003-032254. J Clin Endocrinol Metab. 2004. PMID: 15126585 No abstract available.

8

Osteoporosis in children and adolescents: etiology and management.

Baroncelli GI, Bertelloni S, Sodini F, Saggese G. Baroncelli GI, et al. Paediatr Drugs. 2005;7(5):295-323. doi: 10.2165/00148581-200507050-00003. Paediatr Drugs. 2005. PMID: 16220996 Review.

9

Genetic advances, biochemical and clinical features and critical approach to treatment of patients with X-linked hypophosphatemic rickets.

Baroncelli GI, Bertelloni S, Sodini F, Galli L, Vanacore T, Fiore L, Saggese G. Baroncelli GI, et al. Pediatr Endocrinol Rev. 2004 Jun;1(4):361-79. Pediatr Endocrinol Rev. 2004. PMID: 16437029 Review.

10

17beta-hydroxysteroid dehydrogenase-3 deficiency: a rare endocrine cause of male-to-female sex reversal.

Bertelloni S, Maggio MC, Federico G, Baroncelli G, Hiort O. Bertelloni S, et al. Gynecol Endocrinol. 2006 Sep;22(9):488-94. doi: 10.1080/09513590600921358. Gynecol Endocrinol. 2006. PMID: 17071532

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