Pasqualini T - Search Results

1

Genetic characterization of a large cohort of Argentine 21-hydroxylase Deficiency.

Fernández CS, Taboas M, Bruque CD, Benavides-Mori B, Belli S, Stivel M, Oneto A, Pasqualini T, Delea M, Espeche LD, Kolomenski JE, Alba L, Buzzalino N, Dain L. Fernández CS, et al. Among authors: pasqualini t. Clin Endocrinol (Oxf). 2020 Jul;93(1):19-27. doi: 10.1111/cen.14190. Epub 2020 May 3. Clin Endocrinol (Oxf). 2020. PMID: 32289882

2

Classical and nonclassical 21-hydroxylase deficiency: a molecular study of Argentine patients.

Dain LB, Buzzalino ND, Oneto A, Belli S, Stivel M, Pasqualini T, Minutolo C, Charreau EH, Alba LG. Dain LB, et al. Among authors: pasqualini t. Clin Endocrinol (Oxf). 2002 Feb;56(2):239-45. doi: 10.1046/j.0300-0664.2001.01419.x. Clin Endocrinol (Oxf). 2002. PMID: 11874416

3

Congenital adrenal hyperplasia clinical characteristics and genotype in newborn, childhood and adolescence.

Pasqualini T, Alonso G, Tomasini R, Galich AM, Buzzalino N, Fernandez C, Minutolo C, Alba L, Dain L. Pasqualini T, et al. Medicina (B Aires). 2007;67(3):253-61. Medicina (B Aires). 2007. PMID: 17628913

4

Misregulation effect of a novel allelic variant in the Z promoter region found in cis with the CYP21A2 p.P482S mutation: implications for 21-hydroxylase deficiency.

Fernández CS, Bruque CD, Taboas M, Buzzalino ND, Espeche LD, Pasqualini T, Charreau EH, Alba LG, Ghiringhelli PD, Dain L. Fernández CS, et al. Among authors: pasqualini t. Endocrine. 2015 Sep;50(1):72-8. doi: 10.1007/s12020-015-0680-0. Epub 2015 Jul 17. Endocrine. 2015. PMID: 26184415

5

[Final height in symptomatic boys with late-onset adrenal hyperplasia (LOCAH), treated with glucocorticoids. Clinical cases].

Pasqualini T, Alonso G, Fernández C, Buzzalino N, Dain L. Pasqualini T, et al. Arch Argent Pediatr. 2013 Apr;111(2):e35-8. doi: 10.5546/aap.2013.e35. Arch Argent Pediatr. 2013. PMID: 23568073 Free article. Spanish.

6

[Pediatric emergency: adrenal insufficiency and adrenal crisis].

Martínez A, Pasqualini T, Stivel M, Heinrich JJ. Martínez A, et al. Among authors: pasqualini t. Arch Argent Pediatr. 2010 Apr;108(2):167-70. doi: 10.1590/S0325-00752010000200018. Arch Argent Pediatr. 2010. PMID: 20467714 Free article. Spanish.

7

Clinical Presentation of Klinefelter's Syndrome: Differences According to Age.

Pacenza N, Pasqualini T, Gottlieb S, Knoblovits P, Costanzo PR, Stewart Usher J, Rey RA, Martínez MP, Aszpis S. Pacenza N, et al. Among authors: pasqualini t. Int J Endocrinol. 2012;2012:324835. doi: 10.1155/2012/324835. Epub 2012 Jan 12. Int J Endocrinol. 2012. PMID: 22291701 Free PMC article.

8

Association of Turner's syndrome and Swyer's syndrome in the same family.

Copelli SB, Pasqualini T. Copelli SB, et al. Among authors: pasqualini t. J Pediatr Endocrinol Metab. 2000 May;13(5):557-9. doi: 10.1515/jpem.2000.13.5.557. J Pediatr Endocrinol Metab. 2000. PMID: 10803875

9

Thyroid function and serum IGF-1 in children before and after liver transplantation.

Pasqualini T, Fainstein-Day P, Gutman R, Balzaretti M, D'Agostino D. Pasqualini T, et al. J Pediatr Endocrinol. 1994 Oct-Dec;7(4):343-8. doi: 10.1515/jpem.1994.7.4.343. J Pediatr Endocrinol. 1994. PMID: 7735373 Clinical Trial.

10

Bisphosphonates in children with osteogenesis imperfecta may improve bone mineralization but not bone strength. Report of two patients.

Roldán EJ, Pasqualini T, Plantalech L. Roldán EJ, et al. Among authors: pasqualini t. J Pediatr Endocrinol Metab. 1999 Jul-Aug;12(4):555-9. doi: 10.1515/jpem.1999.12.4.555. J Pediatr Endocrinol Metab. 1999. PMID: 10417973 No abstract available.

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