Baroncelli GI - Search Results

1

Characterization of a complex rearrangement of a chromosome 20 by FISH and array CGH.

Bertini V, Valetto A, Baroncelli GI, Simi P. Bertini V, et al. Among authors: baroncelli gi. Eur J Med Genet. 2011 Jul-Aug;54(4):e419-24. doi: 10.1016/j.ejmg.2011.03.004. Epub 2011 Mar 24. Eur J Med Genet. 2011. PMID: 21440097

2

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.

3

IGF-I generation test in prepubertal children with Noonan syndrome due to mutations in the PTPN11 gene.

Bertelloni S, Baroncelli GI, Dati E, Ghione S, Baldinotti F, Toschi B, Simi P. Bertelloni S, et al. Among authors: baroncelli gi. Hormones (Athens). 2013 Jan-Mar;12(1):86-92. doi: 10.1007/BF03401289. Hormones (Athens). 2013. PMID: 23624134 Free article.

4

NR5A1 gene mutations: clinical, endocrine and genetic features in two girls with 46,XY disorder of sex development.

Bertelloni S, Dati E, Baldinotti F, Toschi B, Marrocco G, Sessa MR, Michelucci A, Simi P, Baroncelli GI. Bertelloni S, et al. Among authors: baroncelli gi. Horm Res Paediatr. 2014;81(2):104-8. doi: 10.1159/000354990. Epub 2014 Jan 16. Horm Res Paediatr. 2014. PMID: 24434652

5

Long-term growth hormone treatment in a boy with 45,X/46,X,idic(Yp) mixed gonadal dysgenesis: comparison with growth pattern of an untreated patient.

Bertelloni S, Dati E, Valetto A, Bertini V, Danti A, Baroncelli GI. Bertelloni S, et al. Among authors: baroncelli gi. Hormones (Athens). 2015 Jan-Mar;14(1):142-7. doi: 10.14310/horm.2002.1498. Hormones (Athens). 2015. PMID: 25402381 Free article.

6

Novel Familial Variant of the Desert Hedgehog Gene: Clinical Findings in Two Sisters with 46,XY Gonadal Dysgenesis or 46,XX Karyotype and Literature Review.

Baldinotti F, Cavallaro T, Dati E, Baroncelli GI, Bertini V, Valetto A, Massart F, Fabrizi GM, Zanette G, Peroni D, Bertelloni S. Baldinotti F, et al. Among authors: baroncelli gi. Horm Res Paediatr. 2018;89(3):141-149. doi: 10.1159/000485507. Epub 2018 Feb 22. Horm Res Paediatr. 2018. PMID: 29471294 Review.

7

Clinical, Immunological, and Genetic Findings in a Cohort of Patients with the DiGeorge Phenotype without 22q11.2 Deletion.

Alberio AMQ, Legitimo A, Bertini V, Baroncelli GI, Costagliola G, Valetto A, Consolini R. Alberio AMQ, et al. Among authors: baroncelli gi. J Clin Med. 2022 Apr 5;11(7):2025. doi: 10.3390/jcm11072025. J Clin Med. 2022. PMID: 35407632 Free PMC article.

8

Longitudinal follow up of a boy affected by Pol III-related leukodystrophy: a detailed phenotype description.

Battini R, Bertelloni S, Astrea G, Casarano M, Travaglini L, Baroncelli G, Pasquariello R, Bertini E, Cioni G. Battini R, et al. BMC Med Genet. 2015 Jul 25;16:53. doi: 10.1186/s12881-015-0203-0. BMC Med Genet. 2015. PMID: 26204956 Free PMC article.

9

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.

10

Analysis of quantitative ultrasound graphic trace and derived variables assessed at proximal phalanges of the hand in healthy subjects and in patients with cerebral palsy or juvenile idiopathic arthritis. A pilot study.

Baroncelli GI, Battini R, Bertelloni S, Brunori E, de Terlizzi F, Vierucci F, Cipriani P, Cioni G, Saggese G. Baroncelli GI, et al. Bone. 2010 Jan;46(1):182-9. doi: 10.1016/j.bone.2009.09.010. Epub 2009 Sep 17. Bone. 2010. PMID: 19772958

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