Livadas S - Search Results

1

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

2

Insufficient adrenarche in patients with combined pituitary hormone deficiency caused by a PROP-1 gene defect.

Voutetakis A, Livadas S, Sertedaki A, Maniati-Christidi M, Dacou-Voutetakis C. Voutetakis A, et al. Among authors: livadas s. J Pediatr Endocrinol Metab. 2001 Sep-Oct;14(8):1107-11. doi: 10.1515/jpem-2001-0806. J Pediatr Endocrinol Metab. 2001. PMID: 11592567

3

Assessment of thyroid function in two hundred patients with beta-thalassemia major.

Zervas A, Katopodi A, Protonotariou A, Livadas S, Karagiorga M, Politis C, Tolis G. Zervas A, et al. Among authors: livadas s. Thyroid. 2002 Feb;12(2):151-4. doi: 10.1089/105072502753522383. Thyroid. 2002. PMID: 11916284

4

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. Among authors: livadas s. Clin Pediatr (Phila). 2003 Jan-Feb;42(1):59-65. doi: 10.1177/000992280304200109. Clin Pediatr (Phila). 2003. PMID: 12635983

5

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.

6

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. Among authors: livadas s. Eur J Endocrinol. 2004 Mar;150(3):257-64. doi: 10.1530/eje.0.1500257. Eur J Endocrinol. 2004. PMID: 15012608

7

Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe.

Voutetakis A, Argyropoulou M, Sertedaki A, Livadas S, Xekouki P, Maniati-Christidi M, Bossis I, Thalassinos N, Patronas N, Dacou-Voutetakis C. Voutetakis A, et al. Among authors: livadas s. J Clin Endocrinol Metab. 2004 May;89(5):2200-6. doi: 10.1210/jc.2003-031765. J Clin Endocrinol Metab. 2004. PMID: 15126542

8

Gene symbol: PROP1. Disease: multiple pituitary hormone deficiency.

Sertedaki A, Voutetakis A, Maniati-Christidi A, Kanaka-Gantenbein Ch, Dracopoulou M, Argyropoulou M, Livadas S, Dacou-Voutetakis A, Sertedaki A. Sertedaki A, et al. Among authors: livadas s. Hum Genet. 2004 Jul;115(2):174. Hum Genet. 2004. PMID: 15300986 No abstract available.

9

Ovulation induction and successful pregnancy outcome in two patients with Prop1 gene mutations.

Voutetakis A, Sertedaki A, Livadas S, Maniati-Christidi M, Mademtzis I, Bossis I, Dacou-Voutetakis C, Messinis IE. Voutetakis A, et al. Among authors: livadas s. Fertil Steril. 2004 Aug;82(2):454-7. doi: 10.1016/j.fertnstert.2004.03.026. Fertil Steril. 2004. PMID: 15302300 Free article.

10

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.

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