Kyriakou A - Search Results

1

Gender differences in the prevalence and severity of bone disease in thalassaemia.

Kyriakou A, Savva SC, Savvides I, Pangalou E, Ioannou YS, Christou S, Skordis N. Kyriakou A, et al. Pediatr Endocrinol Rev. 2008 Oct;6 Suppl 1:116-22. Pediatr Endocrinol Rev. 2008. PMID: 19337164

2

Hormonal dysregulation and bones in thalassaemia--an overview.

Skordis N, Efstathiou E, Kyriakou A, Toumba M. Skordis N, et al. Among authors: kyriakou a. Pediatr Endocrinol Rev. 2008 Oct;6 Suppl 1:107-15. Pediatr Endocrinol Rev. 2008. PMID: 19337163 Review.

3

Effect of bisphosphonate treatment on bone mineral density in patients with thalassaemia major.

Skordis N, Ioannou YS, Kyriakou A, Savva SC, Efstathiou E, Savvides I, Christou S. Skordis N, et al. Among authors: kyriakou a. Pediatr Endocrinol Rev. 2008 Oct;6 Suppl 1:144-8. Pediatr Endocrinol Rev. 2008. PMID: 19337169 Clinical Trial.

4

The IVS1-2A>G mutation in the SRD5A2 gene predominates in Cypriot patients with 5α reductase deficiency.

Skordis N, Neocleous V, Kyriakou A, Efstathiou E, Sertedaki A, Philibert P, Phylactou LA, Lumbroso S, Sultan C. Skordis N, et al. Among authors: kyriakou a. J Endocrinol Invest. 2010 Dec;33(11):810-4. doi: 10.1007/BF03350347. Epub 2010 May 28. J Endocrinol Invest. 2010. PMID: 20511729

5

Molecular defects of the CYP21A2 gene in Greek-Cypriot patients with congenital adrenal hyperplasia.

Skordis N, Kyriakou A, Tardy V, Ioannou YS, Varvaresou A, Dracopoulou-Vabouli M, Patsalis PC, Shammas C, Neocleous V, Phylactou LA. Skordis N, et al. Among authors: kyriakou a. Horm Res Paediatr. 2011;75(3):180-6. doi: 10.1159/000320040. Epub 2010 Sep 14. Horm Res Paediatr. 2011. PMID: 20838032

6

Thalassaemia and aberrations of growth and puberty.

Kyriakou A, Skordis N. Kyriakou A, et al. Mediterr J Hematol Infect Dis. 2009 Jul 27;1(1):e2009003. doi: 10.4084/MJHID.2009.003. Mediterr J Hematol Infect Dis. 2009. PMID: 21415985 Free PMC article.

7

The multifactorial origin of growth failure in thalassaemia.

Skordis N, Kyriakou A. Skordis N, et al. Among authors: kyriakou a. Pediatr Endocrinol Rev. 2011 Mar;8 Suppl 2:271-7. Pediatr Endocrinol Rev. 2011. PMID: 21705977 Review.

8

Overview of genetic defects in endocrinopathies in the island of Cyprus; evidence of a founder effect.

Shammas C, Neocleous V, Toumba M, Costi C, Phedonos AA, Efstathiou E, Kyriakou A, Phylactou LA, Skordis N. Shammas C, et al. Among authors: kyriakou a. Genet Test Mol Biomarkers. 2012 Sep;16(9):1073-9. doi: 10.1089/gtmb.2011.0381. Epub 2012 Aug 2. Genet Test Mol Biomarkers. 2012. PMID: 22857144 Review.

9

Genetic defects in the cyp21a2 gene in heterozygous girls with premature adrenarche and adolescent females with hyperandrogenemia.

Neocleous V, Shammas C, Phedonos AP, Karaoli E, Kyriakou A, Toumba M, Phylactou LA, Skordis N. Neocleous V, et al. Among authors: kyriakou a. Georgian Med News. 2012 Sep;(210):40-7. Georgian Med News. 2012. PMID: 23045419 English, Georgian.

10

Genetic defects of the CYP21A2 gene in girls with premature adrenarche.

Skordis N, Shammas C, Phedonos AA, Kyriakou A, Toumba M, Neocleous V, Phylactou LA. Skordis N, et al. Among authors: kyriakou a. J Endocrinol Invest. 2015 May;38(5):535-9. doi: 10.1007/s40618-014-0223-1. Epub 2014 Dec 7. J Endocrinol Invest. 2015. PMID: 25481255

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

123 results

Search Page