Wasniewska M - Search Results

1

Acute suppurative thyroiditis in childhood: relative frequency among thyroid inflammatory diseases*.

Wasniewska M, Vigone MC, Cappa M, Aversa T, Rubino M, De Luca F; Study Group for Thyroid diseases of Italian Society for Pediatric Endocrinology. Wasniewska M, et al. J Endocrinol Invest. 2007 Apr;30(4):346-7. doi: 10.1007/BF03346303. J Endocrinol Invest. 2007. PMID: 17556874 No abstract available.

2

Liver dysfunction associated with congenital hypopituitarism.

Arrigo T, Wasniewska M, Ghizzoni L, Messina MF, Crisafulli G, De Luca F. Arrigo T, et al. Among authors: wasniewska m. J Endocrinol Invest. 2000 Mar;23(3):215-6. doi: 10.1007/BF03343708. J Endocrinol Invest. 2000. PMID: 10803481 Clinical Trial. No abstract available.

3

Three-year prospective evaluation of glucose tolerance, beta-cell function and peripheral insulin sensitivity in non-diabetic patients with thalassemia major.

Messina MF, Lombardo F, Meo A, Miceli M, Wasniewska M, Valenzise M, Ruggeri C, Arrigo T, De Luca F. Messina MF, et al. Among authors: wasniewska m. J Endocrinol Invest. 2002 Jun;25(6):497-501. doi: 10.1007/BF03345490. J Endocrinol Invest. 2002. PMID: 12109619

4

Fistulectomy may not be the first choice treatment in a child with recurrent suppurative thyroiditis.

Ruggeri C, Wasniewska M, Carcione L, De Luca F. Ruggeri C, et al. Among authors: wasniewska m. J Endocrinol Invest. 2004 Feb;27(2):207-8. doi: 10.1007/BF03346269. J Endocrinol Invest. 2004. PMID: 15129819 No abstract available.

5

Increased liver enzymes and hormonal therapies in girls and adolescents with Turner syndrome.

Wasniewska M, Bergamaschi R, Matarazzo P, Predieri B, Bertelloni S, Petri A, Sposito M, Messina MF, De Luca F; Italian Study Group for Turner Syndrome. Wasniewska M, et al. J Endocrinol Invest. 2005 Sep;28(8):720-6. doi: 10.1007/BF03347555. J Endocrinol Invest. 2005. PMID: 16277168

6

Salt wasting phenotype in a compound heterozygous girl with P482S mutation associated with anovel mutation of CYP21 gene (Q481P).

Di Pasquale G, Wasniewska M, Caruso M, Salzano G, Coco M, Lombardo F, De Luca F. Di Pasquale G, et al. Among authors: wasniewska m. J Endocrinol Invest. 2005 Dec;28(11):1038-9. doi: 10.1007/BF03345346. J Endocrinol Invest. 2005. PMID: 16483186 No abstract available.

7

Congenital adenohypophysis aplasia: clinical features and analysis of the transcriptional factors for embryonic pituitary development.

Arrigo T, Wasniewska M, De Luca F, Valenzise M, Lombardo F, Vivenza D, Vaccaro T, Coradi E, Biason-Lauber A. Arrigo T, et al. Among authors: wasniewska m. J Endocrinol Invest. 2006 Mar;29(3):208-13. doi: 10.1007/BF03345541. J Endocrinol Invest. 2006. PMID: 16682832

8

Acute suppurative thyroiditis in childhood: spontaneous closure of sinus pyriform fistula may occur even very early.

Wasniewska M, Vigone MC, Cappa M, Cassio A, Scognamillo R, Aversa T, Rubino M, De Luca F. Wasniewska M, et al. J Pediatr Endocrinol Metab. 2007 Jan;20(1):75-7. doi: 10.1515/jpem.2007.20.1.75. J Pediatr Endocrinol Metab. 2007. PMID: 17315532 No abstract available.

9

In Sicilian ethnic group non-classical congenital adrenal hyperplasia is frequently associated with a very mild genotype.

Wasniewska M, Di Pasquale G, Rulli I, Salzano G, Caruso M, Indovina S, Di Pasquale L, Zirilli G, De Luca F. Wasniewska M, et al. J Endocrinol Invest. 2007 Mar;30(3):181-5. doi: 10.1007/BF03347422. J Endocrinol Invest. 2007. PMID: 17505149

10

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: wasniewska m. J Endocrinol Invest. 2007 Oct;30(9):806-7. doi: 10.1007/BF03350823. J Endocrinol Invest. 2007. PMID: 17993777 No abstract available.

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