Mirabelli S - Search Results

1

Early hypertension and prolonged mineralocorticoid therapy discontinuation in a child with salt-wasting 21-hydroxylase deficiency.

Wasniewska M, Valenzise M, Aversa T, Mirabelli S, De Luca F, De Luca FL, Lombardo F. Wasniewska M, et al. Among authors: mirabelli s. J Endocrinol Invest. 2011 Feb;34(2):159-61. doi: 10.1007/BF03347048. J Endocrinol Invest. 2011. PMID: 21502797 No abstract available.

2

Novel nonsense mutation (W22X) in CYP21A2 gene causing salt-wasting congenital adrenal hyperplasia in a compound heterozygous girl.

Di Pasquale L, Indovina S, Wasniewska M, Mirabelli S, Porcelli P, Rulli I, Salzano G, De Luca F. Di Pasquale L, et al. Among authors: mirabelli s. J Endocrinol Invest. 2007 Oct;30(9):806-7. doi: 10.1007/BF03350823. J Endocrinol Invest. 2007. PMID: 17993777 No abstract available.

3

Salt-wasting congenital adrenal hyperplasia: genotypical peculiarities in a Sicilian ethnic group.

Wasniewska M, Caruso M, Indovina S, Crisafulli G, Mirabelli S, Salzano G, Arrigo T, De Luca F. Wasniewska M, et al. Among authors: mirabelli s. J Endocrinol Invest. 2008 Jul;31(7):607-9. doi: 10.1007/BF03345610. J Endocrinol Invest. 2008. PMID: 18787377

4

Novel mutation of CYP21A2 gene (N387K) affecting a non-conserved amino acid residue in exon 9.

Wasniewska M, Mirabelli S, Baldazzi L, Salzano G, Messina MF, Lombardo F, Valenzise M, Arrigo T, De Luca F. Wasniewska M, et al. Among authors: mirabelli s. J Endocrinol Invest. 2009 Jul;32(7):633. doi: 10.1007/BF03346522. Epub 2009 Mar 26. J Endocrinol Invest. 2009. PMID: 19474522 No abstract available.

5

Severe SHOX gene haploinsufficiency in a girl with a novel mutation (M1T) involving the first codon of coding region.

Wasniewska M, Raiola G, Nicoletti A, Galati MC, Messina MF, Mirabelli S, De Luca F. Wasniewska M, et al. Among authors: mirabelli s. J Endocrinol Invest. 2010 Apr;33(4):282-3. doi: 10.1007/BF03345793. Epub 2009 Jul 28. J Endocrinol Invest. 2010. PMID: 19636220 No abstract available.

6

Identification of two novel mutations in the first Sicilian APECED patient with no R203X mutation in AIRE gene and review of Italian APECED genotypes.

Valenzise M, Wasniewska M, Mirabelli S, De Luca F, Cervato S, Betterle C. Valenzise M, et al. Among authors: mirabelli s. Gene. 2012 May 15;499(2):343-6. doi: 10.1016/j.gene.2012.03.032. Epub 2012 Mar 17. Gene. 2012. PMID: 22450362

7

Peculiarities of presentation and evolution over time of Hashimoto's thyroiditis in children and adolescents with Down's syndrome.

Aversa T, Salerno M, Radetti G, Faienza MF, Iughetti L, Corrias A, Predieri B, Mussa A, Mirabelli S, De Luca F, Wasniewska M. Aversa T, et al. Among authors: mirabelli s. Hormones (Athens). 2015 Jul-Sep;14(3):410-6. doi: 10.14310/horm.2002.1574. Hormones (Athens). 2015. PMID: 26188225 Free article.

8

Inhibin B in adolescents and young adults with Turner syndrome.

Messina MF, Aversa T, Salzano G, Costanzo D, Sferlazzas C, Mirabelli S, Zirilli G, Lombardo F. Messina MF, et al. Among authors: mirabelli s. J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1209-14. doi: 10.1515/jpem-2014-0229. J Pediatr Endocrinol Metab. 2015. PMID: 25381942

9

Gut mobilization improves behavioral symptoms and modulates urinary p-cresol in chronically constipated autistic children: A prospective study.

Turriziani L, Ricciardello A, Cucinotta F, Bellomo F, Turturo G, Boncoddo M, Mirabelli S, Scattoni ML, Rossi M, Persico AM. Turriziani L, et al. Among authors: mirabelli s. Autism Res. 2022 Jan;15(1):56-69. doi: 10.1002/aur.2639. Epub 2021 Nov 23. Autism Res. 2022. PMID: 34813183 Free PMC article.

10

The pediatric psychopharmacology of autism spectrum disorder: A systematic review - Part II: The future.

Persico AM, Asta L, Chehbani F, Mirabelli S, Parlatini V, Cortese S, Arango C, Vitiello B. Persico AM, et al. Among authors: mirabelli s. Prog Neuropsychopharmacol Biol Psychiatry. 2024 Oct 28;136:111176. doi: 10.1016/j.pnpbp.2024.111176. Online ahead of print. Prog Neuropsychopharmacol Biol Psychiatry. 2024. PMID: 39490514 Review.

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