Neocleous V - Search Results

1

High carrier frequency of 21-hydroxylase deficiency in Cyprus.

Phedonos AA, Shammas C, Skordis N, Kyriakides TC, Neocleous V, Phylactou LA. Phedonos AA, et al. Among authors: neocleous v. Clin Genet. 2013 Dec;84(6):585-8. doi: 10.1111/cge.12153. Epub 2013 Apr 22. Clin Genet. 2013. PMID: 23600966

2

Distal hereditary motor neuronopathy of the Jerash type.

Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, el-Khateeb M, al-Qudah A, Horany K. Middleton LT, et al. Among authors: neocleous v. Ann N Y Acad Sci. 1999 Sep 14;883:65-8. Ann N Y Acad Sci. 1999. PMID: 10586232

3

Distal hereditary motor neuronopathy of the Jerash type.

Middleton LT, Christodoulou K, Mubaidin A, Zamba E, Tsingis M, Kyriacou K, Abu-Sheikh S, Kyriakides T, Neocleous V, Georgiou DM, el-Khateeb M, al-Qudah A, Horany K. Middleton LT, et al. Among authors: neocleous v. Ann N Y Acad Sci. 1999 Sep 14;883:439-42. Ann N Y Acad Sci. 1999. PMID: 10586267 No abstract available.

4

Description of the first two seemingly unrelated Greek Cypriot families with a common C618R RET proto-oncogene mutation.

Neocleous V, Passalaris T, Spanou E, Kitsios P, Skordis N, Deltas CC. Neocleous V, et al. Genet Test. 2004 Summer;8(2):163-8. doi: 10.1089/gte.2004.8.163. Genet Test. 2004. PMID: 15345114

5

Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Greek Cypriot population.

Neocleous V, Portides G, Anastasiadou V, Phylactou LA. Neocleous V, et al. Int J Pediatr Otorhinolaryngol. 2006 Aug;70(8):1473-7. doi: 10.1016/j.ijporl.2006.03.014. Epub 2006 May 19. Int J Pediatr Otorhinolaryngol. 2006. PMID: 16713631

6

High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.

Neocleous V, Aspris A, Shahpenterian V, Nicolaou V, Panagi C, Ioannou I, Kyamides Y, Anastasiadou V, Phylactou LA. Neocleous V, et al. Genet Test. 2006 Winter;10(4):285-9. doi: 10.1089/gte.2006.10.285. Genet Test. 2006. PMID: 17253936

7

Rare mutations in the CYP21A2 gene detected in congenital adrenal hyperplasia.

Neocleous V, Ioannou YS, Bartsota M, Costi C, Skordis N, Phylactou LA. Neocleous V, et al. Clin Biochem. 2009 Sep;42(13-14):1363-7. doi: 10.1016/j.clinbiochem.2009.05.015. Epub 2009 Jun 6. Clin Biochem. 2009. PMID: 19501079

8

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: neocleous v. J Endocrinol Invest. 2010 Dec;33(11):810-4. doi: 10.1007/BF03350347. Epub 2010 May 28. J Endocrinol Invest. 2010. PMID: 20511729

9

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: neocleous v. Horm Res Paediatr. 2011;75(3):180-6. doi: 10.1159/000320040. Epub 2010 Sep 14. Horm Res Paediatr. 2011. PMID: 20838032

10

RET proto-oncogene mutations are restricted to codon 618 in Cypriot families with multiple endocrine neoplasia 2.

Neocleous V, Skordis N, Portides G, Efstathiou E, Costi C, Ioannou N, Pantzaris M, Anastasiadou V, Deltas C, Phylactou LA. Neocleous V, et al. J Endocrinol Invest. 2011 Nov;34(10):764-9. doi: 10.3275/7605. Epub 2011 Mar 21. J Endocrinol Invest. 2011. PMID: 21422799

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