Baronio F - Search Results

1

CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency.

Balsamo A, Cicognani A, Baldazzi L, Barbaro M, Baronio F, Gennari M, Bal M, Cassio A, Kontaxaki K, Cacciari E. Balsamo A, et al. Among authors: baronio f. J Clin Endocrinol Metab. 2003 Dec;88(12):5680-8. doi: 10.1210/jc.2003-030123. J Clin Endocrinol Metab. 2003. PMID: 14671153

2

Outcome of COVID-19 infections in patients with adrenal insufficiency and excess.

Nowotny HF, Bryce J, Ali SR, Giordano R, Baronio F, Chifu I, Tschaidse L, Cools M, van den Akker EL, Falhammar H, Appelman-Dijkstra NM, Persani L, Beccuti G, Ross IL, Grozinsky-Glasberg S, Pereira AM, Husebye ES, Hahner S, Faisal Ahmed S, Reisch N. Nowotny HF, et al. Among authors: baronio f. Endocr Connect. 2023 Mar 10;12(4):e220416. doi: 10.1530/EC-22-0416. Print 2023 Apr 1. Endocr Connect. 2023. PMID: 36715679 Free PMC article.

3

A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism.

Balsamo A, Antelli A, Baldazzi L, Baronio F, Lazareva D, Cassio A, Cicognani A. Balsamo A, et al. Among authors: baronio f. Am J Med Genet A. 2005 Jun 15;135(3):292-6. doi: 10.1002/ajmg.a.30689. Am J Med Genet A. 2005. PMID: 15884018

4

Height as a risk factor for osteosarcoma.

Longhi A, Pasini A, Cicognani A, Baronio F, Pellacani A, Baldini N, Bacci G. Longhi A, et al. Among authors: baronio f. J Pediatr Hematol Oncol. 2005 Jun;27(6):314-8. doi: 10.1097/01.mph.0000169251.57611.8e. J Pediatr Hematol Oncol. 2005. PMID: 15956884

5

Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes.

Balsamo A, Wasniewska M, Di Pasquale G, Salzano G, Baronio F, Bombaci S, De Luca F. Balsamo A, et al. Among authors: baronio f. Eur J Pediatr. 2006 Jun;165(6):380-3. doi: 10.1007/s00431-005-0075-y. Epub 2006 Mar 7. Eur J Pediatr. 2006. PMID: 16520942

6

Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency.

Zucchini S, Pirazzoli P, Baronio F, Gennari M, Bal MO, Balsamo A, Gualandi S, Cicognani A. Zucchini S, et al. Among authors: baronio f. J Clin Endocrinol Metab. 2006 Nov;91(11):4271-6. doi: 10.1210/jc.2006-0383. Epub 2006 Aug 15. J Clin Endocrinol Metab. 2006. PMID: 16912138 Clinical Trial.

7

Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1.

Balsamo A, Cicognani A, Gennari M, Sippell WG, Menabò S, Baronio F, Riepe FG. Balsamo A, et al. Among authors: baronio f. Eur J Endocrinol. 2007 Feb;156(2):249-56. doi: 10.1530/eje.1.02330. Eur J Endocrinol. 2007. PMID: 17287415

8

Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis.

Corrias A, Cassio A, Weber G, Mussa A, Wasniewska M, Rapa A, Gastaldi R, Einaudi S, Baronio F, Vigone MC, Messina MF, Bal M, Bona G, de Sanctis C; Study Group for Thyroid Diseases of Italian Society for Pediatric Endocrinology and Diabetology (SIEDP/ISPED). Corrias A, et al. Among authors: baronio f. Arch Pediatr Adolesc Med. 2008 Jun;162(6):526-31. doi: 10.1001/archpedi.162.6.526. Arch Pediatr Adolesc Med. 2008. PMID: 18524742

9

Long-term clinical significance of thyroid autoimmunity in children with celiac disease.

Cassio A, Ricci G, Baronio F, Miniaci A, Bal M, Bigucci B, Conti V, Cicognani A. Cassio A, et al. Among authors: baronio f. J Pediatr. 2010 Feb;156(2):292-5. doi: 10.1016/j.jpeds.2009.08.047. Epub 2009 Oct 20. J Pediatr. 2010. PMID: 19846116

10

The SHOX gene: a new indication for GH treatment.

Cicognani A, Pirazzoli P, Nicoletti A, Baronio F, Conti V, Bonetti S. Cicognani A, et al. Among authors: baronio f. J Endocrinol Invest. 2010 Jun;33(6 Suppl):15-8. J Endocrinol Invest. 2010. PMID: 21057180

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