Toschi B - Search Results

1

Correction to: The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion.

Baroncelli GI, Carlucci G, Freri E, Giuca MR, Guarnieri V, Navarra G, Toschi B, Mora S. Baroncelli GI, et al. Among authors: toschi b. J Endocrinol Invest. 2024 Dec;47(12):3137. doi: 10.1007/s40618-024-02403-5. J Endocrinol Invest. 2024. PMID: 38853196 No abstract available.

2

Constitutional FLCN mutations in patients with suspected Birt-Hogg-Dubé syndrome ascertained for non-cutaneous manifestations.

Maffé A, Toschi B, Circo G, Giachino D, Giglio S, Rizzo A, Carloni A, Poletti V, Tomassetti S, Ginardi C, Ungari S, Genuardi M. Maffé A, et al. Among authors: toschi b. Clin Genet. 2011 Apr;79(4):345-54. doi: 10.1111/j.1399-0004.2010.01480.x. Clin Genet. 2011. PMID: 20618353

3

Hypophosphatemic rickets.

Baroncelli GI, Toschi B, Bertelloni S. Baroncelli GI, et al. Among authors: toschi b. Curr Opin Endocrinol Diabetes Obes. 2012 Dec;19(6):460-7. doi: 10.1097/MED.0b013e328358be97. Curr Opin Endocrinol Diabetes Obes. 2012. PMID: 23108197 Review.

4

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: toschi b. Hormones (Athens). 2013 Jan-Mar;12(1):86-92. doi: 10.1007/BF03401289. Hormones (Athens). 2013. PMID: 23624134 Free article.

5

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: toschi b. Horm Res Paediatr. 2014;81(2):104-8. doi: 10.1159/000354990. Epub 2014 Jan 16. Horm Res Paediatr. 2014. PMID: 24434652

6

Growth in Boys with 45,X/46,XY Mosaicism: Effect of Growth Hormone Treatment on Statural Growth.

Bertelloni S, Baroncelli GI, Massart F, Toschi B. Bertelloni S, et al. Among authors: toschi b. Sex Dev. 2015;9(4):183-9. doi: 10.1159/000441342. Epub 2015 Nov 4. Sex Dev. 2015. PMID: 26529521 Free article. Review.

7

Short Stature in Isodicentric Y Chromosome and Three Copies of the SHOX Gene: Clinical Report and Review of Literature.

Valetto A, Bertini V, Michelucci A, Toschi B, Dati E, Baroncelli GI, Bertelloni S. Valetto A, et al. Among authors: toschi b. Mol Syndromol. 2016 Apr;7(1):19-25. doi: 10.1159/000444430. Epub 2016 Mar 12. Mol Syndromol. 2016. PMID: 27194969 Free PMC article.

8

Significant Improvement of Clinical Symptoms, Bone Lesions, and Bone Turnover after Long-Term Zoledronic Acid Treatment in Patients with a Severe Form of Camurati-Engelmann Disease.

Baroncelli GI, Ferretti E, Pini CM, Toschi B, Consolini R, Bertelloni S. Baroncelli GI, et al. Among authors: toschi b. Mol Syndromol. 2017 Nov;8(6):294-302. doi: 10.1159/000479859. Epub 2017 Sep 9. Mol Syndromol. 2017. PMID: 29230158 Free PMC article.

9

Pulp chamber features, prevalence of abscesses, disease severity, and PHEX mutation in X-linked hypophosphatemic rickets.

Baroncelli GI, Zampollo E, Manca M, Toschi B, Bertelloni S, Michelucci A, Isola A, Bulleri A, Peroni D, Giuca MR. Baroncelli GI, et al. Among authors: toschi b. J Bone Miner Metab. 2021 Mar;39(2):212-223. doi: 10.1007/s00774-020-01136-8. Epub 2020 Aug 8. J Bone Miner Metab. 2021. PMID: 32772199

10

The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion.

Baroncelli GI, Carlucci G, Freri E, Giuca MR, Guarnieri V, Navarra G, Toschi B, Mora S. Baroncelli GI, et al. Among authors: toschi b. J Endocrinol Invest. 2024 Mar;47(3):739-747. doi: 10.1007/s40618-023-02199-w. Epub 2023 Sep 26. J Endocrinol Invest. 2024. PMID: 37752373 Free PMC article.

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