Vaiani E - Search Results

1

Effectiveness of rhGH treatment on adult height in GH-deficient childhood survivors of medulloblastoma.

Ciaccio M, Gil S, Guercio G, Vaiani E, Alderete D, Palladino M, Warman DM, Rivarola MA, Belgorosky A. Ciaccio M, et al. Among authors: vaiani e. Horm Res Paediatr. 2010;73(4):281-6. doi: 10.1159/000284393. Epub 2010 Mar 9. Horm Res Paediatr. 2010. PMID: 20215775

2

Hypothalamic-pituitary-testicular function in prepubertal children with chronic liver disease.

Vaiani E, Ciocca M, Cuarterolo M, Imventarza O, Rivarola MA, Belgorosky A. Vaiani E, et al. J Pediatr Endocrinol Metab. 2002 Mar;15(3):289-95. doi: 10.1515/jpem.2002.15.3.289. J Pediatr Endocrinol Metab. 2002. PMID: 11924931

3

Hypothalamic-pituitary-ovarian axis during infancy, early and late prepuberty in an aromatase-deficient girl who is a compound heterocygote for two new point mutations of the CYP19 gene.

Belgorosky A, Pepe C, Marino R, Guercio G, Saraco N, Vaiani E, Rivarola MA. Belgorosky A, et al. Among authors: vaiani e. J Clin Endocrinol Metab. 2003 Nov;88(11):5127-31. doi: 10.1210/jc.2003-030433. J Clin Endocrinol Metab. 2003. PMID: 14602738

4

Unexpected peripheral markers of thyroid function in a patient with a novel mutation of the MCT8 thyroid hormone transporter gene.

Herzovich V, Vaiani E, Marino R, Dratler G, Lazzati JM, Tilitzky S, Ramirez P, Iorcansky S, Rivarola MA, Belgorosky A. Herzovich V, et al. Among authors: vaiani e. Horm Res. 2007;67(1):1-6. doi: 10.1159/000095805. Epub 2006 Sep 15. Horm Res. 2007. PMID: 16974106

5

The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues.

Pepe CM, Saraco NI, Baquedano MS, Guercio G, Vaiani E, Marino R, Pandey AV, Flück CE, Rivarola MA, Belgorosky A. Pepe CM, et al. Among authors: vaiani e. Clin Endocrinol (Oxf). 2007 Nov;67(5):698-705. doi: 10.1111/j.1365-2265.2007.02948.x. Epub 2007 Jul 2. Clin Endocrinol (Oxf). 2007. PMID: 17608756

6

[Exon 5 alternative splicing of the cytochrome P450 aromatase could be a regulatory mechanism for estrogen production in humans].

Pepe CM, Saraco NI, Baquedano MS, Guercio G, Vaiani E, Berensztein E, Rivarola MA, Belgorosky A. Pepe CM, et al. Among authors: vaiani e. Medicina (B Aires). 2007;67(4):369-73. Medicina (B Aires). 2007. PMID: 17891933 Spanish.

7

Thyroid axis dysfunction in patients with Prader-Willi syndrome during the first 2 years of life.

Vaiani E, Herzovich V, Chaler E, Chertkoff L, Rivarola MA, Torrado M, Belgorosky A. Vaiani E, et al. Clin Endocrinol (Oxf). 2010 Oct;73(4):546-50. doi: 10.1111/j.1365-2265.2010.03840.x. Clin Endocrinol (Oxf). 2010. PMID: 20560980

8

Effectiveness of rhGH treatment on final height of renal-transplant recipients in childhood.

Gil S, Vaiani E, Guercio G, Ciaccio M, Turconi A, Delgado N, Rivarola MA, Belgorosky A. Gil S, et al. Among authors: vaiani e. Pediatr Nephrol. 2012 Jun;27(6):1005-9. doi: 10.1007/s00467-011-2090-8. Epub 2012 Jan 26. Pediatr Nephrol. 2012. PMID: 22278170

9

Unique dominant negative mutation in the N-terminal mitochondrial targeting sequence of StAR, causing a variant form of congenital lipoid adrenal hyperplasia.

Baquedano MS, Guercio G, Marino R, Berensztein E, Costanzo M, Bailez M, Vaiani E, Maceiras M, Ramirez P, Chaler E, Rivarola MA, Belgorosky A. Baquedano MS, et al. Among authors: vaiani e. J Clin Endocrinol Metab. 2013 Jan;98(1):E153-61. doi: 10.1210/jc.2012-2865. Epub 2012 Nov 21. J Clin Endocrinol Metab. 2013. PMID: 23175692

10

[Novel heterozygous mutation in the steroidogenic acute regulatory protein gene in a 46,XY patient with congenital lipoid adrenal hyperplasia].

Baquedano MS, Guercio G, Marino R, Berensztein E, Costanzo M, Ramírez P, Bailez M, Vaiani E, Maceiras M, Rivarola MA, Belgorosky A. Baquedano MS, et al. Among authors: vaiani e. Medicina (B Aires). 2013;73(4):297-302. Medicina (B Aires). 2013. PMID: 23924526 Free article. Spanish.

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