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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1974 1
1975 4
1976 10
1977 14
1978 6
1979 2
1980 3
1981 3
1982 4
1983 1
1984 4
1989 1
1995 2
1996 4
1997 3
1998 5
1999 2
2000 4
2001 3
2002 3
2003 3
2004 2
2005 1
2006 1
2007 1
2008 4
2009 1
2010 4
2011 5
2012 4
2013 6
2014 2
2015 6
2016 1
2017 2
2018 1
2021 0
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118 results
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Page 1
Molecular genetics of familial hematuric diseases.
Deltas C, Pierides A, Voskarides K. Deltas C, et al. Among authors: pierides a. Nephrol Dial Transplant. 2013 Dec;28(12):2946-60. doi: 10.1093/ndt/gft253. Epub 2013 Sep 17. Nephrol Dial Transplant. 2013. PMID: 24046192 Review.
The role of molecular genetics in diagnosing familial hematuria(s).
Deltas C, Pierides A, Voskarides K. Deltas C, et al. Among authors: pierides a. Pediatr Nephrol. 2012 Aug;27(8):1221-31. doi: 10.1007/s00467-011-1935-5. Epub 2011 Jun 19. Pediatr Nephrol. 2012. PMID: 21688191 Free PMC article. Review.
RAAS inhibition and the course of Alport syndrome.
Savva I, Pierides A, Deltas C. Savva I, et al. Among authors: pierides a. Pharmacol Res. 2016 May;107:205-210. doi: 10.1016/j.phrs.2016.03.017. Epub 2016 Mar 16. Pharmacol Res. 2016. PMID: 26995302 Review.
A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general population.
Voskarides K, Stefanou C, Pieri M, Demosthenous P, Felekkis K, Arsali M, Athanasiou Y, Xydakis D, Stylianou K, Daphnis E, Goulielmos G, Loizou P, Savige J, Höhne M, Völker LA, Benzing T, Maxwell PH, Gale DP, Gorski M, Böger C, Kollerits B, Kronenberg F, Paulweber B, Zavros M, Pierides A, Deltas C. Voskarides K, et al. Among authors: pierides a. PLoS One. 2017 Mar 23;12(3):e0174274. doi: 10.1371/journal.pone.0174274. eCollection 2017. PLoS One. 2017. PMID: 28334007 Free PMC article.
Ketotic hypoglycaemia of childhood.
Pierides AM, Anderson J, Stansfeld JM. Pierides AM, et al. Postgrad Med J. 1975 Oct;51(600):737-41. doi: 10.1136/pgmj.51.600.737. Postgrad Med J. 1975. PMID: 1197182 Free PMC article.
Renal bone disease--what is it and why does it happen?
Feest TG, Ward MK, Ellis HA, Conceicao S, Pierides AM, Aird E, Simpson W, Cook DB, Kerr DN. Feest TG, et al. Among authors: pierides am. Clin Endocrinol (Oxf). 1977 Dec;7 Suppl:19s-23s. doi: 10.1111/j.1365-2265.1977.tb03357.x. Clin Endocrinol (Oxf). 1977. PMID: 342144 Review. No abstract available.
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis.
Gale DP, de Jorge EG, Cook HT, Martinez-Barricarte R, Hadjisavvas A, McLean AG, Pusey CD, Pierides A, Kyriacou K, Athanasiou Y, Voskarides K, Deltas C, Palmer A, Frémeaux-Bacchi V, de Cordoba SR, Maxwell PH, Pickering MC. Gale DP, et al. Among authors: pierides a. Lancet. 2010 Sep 4;376(9743):794-801. doi: 10.1016/S0140-6736(10)60670-8. Epub 2010 Aug 25. Lancet. 2010. PMID: 20800271 Free PMC article.
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