Dacou-Voutetakis C - Search Results

1

Gonadoblastoma in a patient with del(9)(p22) and sex reversal: report of a case and review of the literature.

Livadas S, Mavrou A, Sofocleous C, van Vliet-Constantinidou C, Dracopoulou M, Dacou-Voutetakis C. Livadas S, et al. Cancer Genet Cytogenet. 2003 Jun;143(2):174-7. doi: 10.1016/s0165-4608(02)00849-x. Cancer Genet Cytogenet. 2003. PMID: 12781454 Review.

2

Spontaneous pregnancy and birth of a normal female from a woman with Turner syndrome and elevated gonadotropins.

Livadas S, Xekouki P, Kafiri G, Voutetakis A, Maniati-Christidi M, Dacou-Voutetakis C. Livadas S, et al. Fertil Steril. 2005 Mar;83(3):769-72. doi: 10.1016/j.fertnstert.2004.11.007. Fertil Steril. 2005. PMID: 15749515 Free article.

3

Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X).

Voutetakis A, Maniati-Christidi M, Kanaka-Gantenbein C, Dracopoulou M, Argyropoulou M, Livadas S, Dacou-Voutetakis C, Sertedaki A. Voutetakis A, et al. Eur J Endocrinol. 2004 Mar;150(3):257-64. doi: 10.1530/eje.0.1500257. Eur J Endocrinol. 2004. PMID: 15012608

4

Non-classical congenital adrenal hyperplasia.

Dacou-Voutetakis C, Dracopoulou M. Dacou-Voutetakis C, et al. Pediatr Endocrinol Rev. 2006 Jan;3 Suppl 1:195-7. Pediatr Endocrinol Rev. 2006. PMID: 16641859

5

High incidence of molecular defects of the CYP21 gene in patients with premature adrenarche.

Dacou-Voutetakis C, Dracopoulou M. Dacou-Voutetakis C, et al. J Clin Endocrinol Metab. 1999 May;84(5):1570-4. doi: 10.1210/jcem.84.5.5683. J Clin Endocrinol Metab. 1999. PMID: 10323382

6

Elevated coagulation and inflammatory markers in adolescents with a history of premature adrenarche.

Livadas S, Dracopoulou M, Vasileiadi K, Lazaropoulou C, Magiakou MA, Xekouki P, Voutetakis A, Kanaka-Gantenbein C, Papassotiriou I, Stefanadis C, Chrousos GP, Dacou-Voutetakis C. Livadas S, et al. Metabolism. 2009 Apr;58(4):576-81. doi: 10.1016/j.metabol.2008.12.002. Metabolism. 2009. PMID: 19303981

7

A favorable metabolic and antiatherogenic profile in carriers of CYP21A2 gene mutations supports the theory of a survival advantage in this population.

Livadas S, Dracopoulou M, Lazaropoulou C, Papassotiriou I, Sertedaki A, Angelopoulos GN, Chrousos GP, Dacou-Voutetakis C. Livadas S, et al. Horm Res. 2009;72(6):337-43. doi: 10.1159/000249161. Epub 2009 Oct 21. Horm Res. 2009. PMID: 19844122

8

Prevalence of thyroid dysfunction in Turner's syndrome: a long-term follow-up study and brief literature review.

Livadas S, Xekouki P, Fouka F, Kanaka-Gantenbein C, Kaloumenou I, Mavrou A, Constantinidou N, Dacou-Voutetakis C. Livadas S, et al. Thyroid. 2005 Sep;15(9):1061-6. doi: 10.1089/thy.2005.15.1061. Thyroid. 2005. PMID: 16187915

9

Human growth hormone and gonadotropin releasing hormone analog combination therapy increases predicted height in short normal girls.

Maniati-Christidi M, Livadas S, Voutetakis A, Tolis G, Dacou-Voutetakis C. Maniati-Christidi M, et al. Clin Pediatr (Phila). 2003 Jan-Feb;42(1):59-65. doi: 10.1177/000992280304200109. Clin Pediatr (Phila). 2003. PMID: 12635983

10

Low TSH congenital hypothyroidism: identification of a novel mutation of the TSH beta-subunit gene in one sporadic case (C85R) and of mutation Q49stop in two siblings with congenital hypothyroidism.

Sertedaki A, Papadimitriou A, Voutetakis A, Dracopoulou M, Maniati-Christidi M, Dacou-Voutetakis C. Sertedaki A, et al. Pediatr Res. 2002 Dec;52(6):935-41. doi: 10.1203/00006450-200212000-00020. Pediatr Res. 2002. PMID: 12438673

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

104 results

Search Page

Filters