Tatò L - Search Results

1

Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children.

Teofoli F, Camilot M, Tatò L. Teofoli F, et al. Among authors: tato l. J Endocrinol Invest. 2007 Feb;30(2):163-6. doi: 10.1007/BF03347416. J Endocrinol Invest. 2007. PMID: 17392608

2

Implementation of a congenital hypothyroidism newborn screening procedure with mutation detection on genomic DNA extracted from blood spots: the experience of the Italian northeastern reference center.

Camilot M, Teofoli F, Vincenzi M, Federici F, Perlini S, Tatò L. Camilot M, et al. Among authors: tato l. Genet Test. 2007 Winter;11(4):387-90. doi: 10.1089/gte.2007.0033. Genet Test. 2007. PMID: 18294054

3

Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes.

Camilot M, Teofoli F, Gandini A, Franceschi R, Rapa A, Corrias A, Bona G, Radetti G, Tatò L. Camilot M, et al. Among authors: tato l. Clin Endocrinol (Oxf). 2005 Aug;63(2):146-51. doi: 10.1111/j.1365-2265.2005.02314.x. Clin Endocrinol (Oxf). 2005. PMID: 16060907

4

A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis.

Camilot M, Teofoli F, Longobardi S, Gandini A, Lievore C, Lauriola S, Tatò L. Camilot M, et al. Among authors: tato l. J Endocrinol Invest. 2008 Jan;31(1):1-7. doi: 10.1007/BF03345559. J Endocrinol Invest. 2008. PMID: 18296898

5

Prepubertal serum inhibin B in cryptorchid infants and in monorchid boys with compensatory testicular hypertrophy.

Gaudino R, Cavarzere P, Camilot M, Teofoli F, Zampieri N, Tatò L. Gaudino R, et al. Among authors: tato l. Fertil Steril. 2008 Dec;90(6):2217-21. doi: 10.1016/j.fertnstert.2007.10.017. Epub 2008 Jan 14. Fertil Steril. 2008. PMID: 18191850 Free article.

6

Functional studies of new TSH receptor (TSHr) mutations identified in patients affected by hypothyroidism or isolated hyperthyrotrophinaemia.

De Marco G, Agretti P, Camilot M, Teofoli F, Tatò L, Vitti P, Pinchera A, Tonacchera M. De Marco G, et al. Among authors: tato l. Clin Endocrinol (Oxf). 2009 Feb;70(2):335-8. doi: 10.1111/j.1365-2265.2008.03333.x. Epub 2008 Aug 22. Clin Endocrinol (Oxf). 2009. PMID: 18727713

7

Subclinical hypothyroidism in children and adolescents: a wide range of clinical, biochemical, and genetic factors involved.

Rapa A, Monzani A, Moia S, Vivenza D, Bellone S, Petri A, Teofoli F, Cassio A, Cesaretti G, Corrias A, de Sanctis V, Di Maio S, Volta C, Wasniewska M, Tatò L, Bona G. Rapa A, et al. Among authors: tato l. J Clin Endocrinol Metab. 2009 Jul;94(7):2414-20. doi: 10.1210/jc.2009-0375. Epub 2009 May 5. J Clin Endocrinol Metab. 2009. PMID: 19417038

8

Possible andrologic markers in elevated neonatal 17-hydroxyprogesterone.

Cavarzere P, Vincenzi M, Gaudino R, Franceschi R, Perlini S, Camilot M, Teofoli F, Antoniazzi F, Tatò L. Cavarzere P, et al. Among authors: tato l. Fertil Steril. 2010 Nov;94(6):2350-2. doi: 10.1016/j.fertnstert.2010.04.040. Epub 2010 May 26. Fertil Steril. 2010. PMID: 20537623 Free article.

9

Neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: a report three years into the program.

Cavarzere P, Camilot M, Teofoli F, Tatò L. Cavarzere P, et al. Among authors: tato l. Horm Res. 2005;63(4):180-6. doi: 10.1159/000085021. Epub 2005 Apr 7. Horm Res. 2005. PMID: 15818055

10

Thyroxine hair content in congenital hypothyroidism and hyperthyroidism.

Zamboni G, Camilot M, Francia G, Lauriola S, Arslanoglu I, Isguven P, Tatò L. Zamboni G, et al. Among authors: tato l. J Pediatr Endocrinol Metab. 2003 Mar;16(3):379-82. doi: 10.1515/jpem.2003.16.3.379. J Pediatr Endocrinol Metab. 2003. PMID: 12705362 Clinical Trial.

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