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Variations in the 3'UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia.
Int J Endocrinol. 2017;2017:8984365. doi: 10.1155/2017/8984365. Epub 2017 Apr 12.
Int J Endocrinol. 2017.
PMID: 28487735
Free PMC article.
Phenotypic variability of hyperandrogenemia in females heterozygous for CYP21A2 mutations.
Neocleous V, Shammas C, Phedonos AA, Phylactou LA, Skordis N.
Neocleous V, et al. Among authors: phedonos aa.
Indian J Endocrinol Metab. 2014 Nov;18(Suppl 1):S72-9. doi: 10.4103/2230-8210.145077.
Indian J Endocrinol Metab. 2014.
PMID: 25538881
Free PMC article.
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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: phedonos aa.
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
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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.
Clin Genet. 2013 Dec;84(6):585-8. doi: 10.1111/cge.12153. Epub 2013 Apr 22.
Clin Genet. 2013.
PMID: 23600966
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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: phedonos aa.
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.
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Characterization of antioxidant/anti-inflammatory properties and apoA-I-containing subpopulations of HDL from family subjects with monogenic low HDL disorders.
Daniil G, Phedonos AA, Holleboom AG, Motazacker MM, Argyri L, Kuivenhoven JA, Chroni A.
Daniil G, et al. Among authors: phedonos aa.
Clin Chim Acta. 2011 Jun 11;412(13-14):1213-20. doi: 10.1016/j.cca.2011.03.011. Epub 2011 Mar 21.
Clin Chim Acta. 2011.
PMID: 21420943
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