De Luca F - Search Results

1

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. Among authors: de luca f. J Endocrinol Invest. 2007 Mar;30(3):181-5. doi: 10.1007/BF03347422. J Endocrinol Invest. 2007. PMID: 17505149

2

TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism.

Santarpia L, Valenzise M, Di Pasquale G, Arrigo T, San Martino G, Cicciò MP, Trimarchi F, De Luca F, Benvenga S. Santarpia L, et al. Among authors: de luca f. J Endocrinol Invest. 2007 Jan;30(1):13-9. doi: 10.1007/BF03347390. J Endocrinol Invest. 2007. PMID: 17318017

3

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

4

Subclinical hypothyroidism: the state of the art.

Arrigo T, Wasniewska M, Crisafulli G, Lombardo F, Messina MF, Rulli I, Salzano G, Valenzise M, Zirilli G, De Luca F. Arrigo T, et al. Among authors: de luca f. J Endocrinol Invest. 2008 Jan;31(1):79-84. doi: 10.1007/BF03345571. J Endocrinol Invest. 2008. PMID: 18296910 Review.

5

In the Italian population sexual dimorphism affects pre-natal thyroid migration but not biochemical severity of gland ectopia and pre-natal bone maturation.

Wasniewska M, Arrigo T, Crisafulli G, Aversa T, Messina MF, Salzano G, De Luca F. Wasniewska M, et al. Among authors: de luca f. J Endocrinol Invest. 2008 Apr;31(4):341-5. doi: 10.1007/BF03346368. J Endocrinol Invest. 2008. PMID: 18475053

6

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: de luca f. J Endocrinol Invest. 2008 Jul;31(7):607-9. doi: 10.1007/BF03345610. J Endocrinol Invest. 2008. PMID: 18787377

7

Increased large artery intima media thickness in adolescents with either classical or non-classical congenital adrenal hyperplasia.

Wasniewska M, Balsamo A, Valenzise M, Manganaro A, Faggioli G, Bombaci S, Conti V, Ferri M, Aversa T, Cicognani A, De Luca F. Wasniewska M, et al. Among authors: de luca f. J Endocrinol Invest. 2013 Jan;36(1):12-5. doi: 10.3275/8194. Epub 2011 Dec 21. J Endocrinol Invest. 2013. PMID: 22189488

8

Phenotypical and genotypical expression of Wolfram syndrome in 12 patients from a Sicilian district where this syndrome might not be so infrequent as generally expected.

Lombardo F, Salzano G, Di Bella C, Aversa T, Pugliatti F, Cara S, Valenzise M, De Luca F, Rigoli L. Lombardo F, et al. Among authors: de luca f. J Endocrinol Invest. 2014 Feb;37(2):195-202. doi: 10.1007/s40618-013-0039-4. Epub 2014 Jan 9. J Endocrinol Invest. 2014. PMID: 24497219

9

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: de luca f. J Endocrinol Invest. 2002 Jun;25(6):497-501. doi: 10.1007/BF03345490. J Endocrinol Invest. 2002. PMID: 12109619

10

Nutritional, glycometabolic and genetic factors affecting menarcheal age in cystic fibrosis.

Arrigo T, De Luca F, Lucanto C, Lombardo M, Rulli I, Salzano G, Lombardo F. Arrigo T, et al. Among authors: de luca f. Diabetes Nutr Metab. 2004 Apr;17(2):114-9. Diabetes Nutr Metab. 2004. PMID: 15244104

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