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Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.
Clin Genet. 2017 Nov;92(5):517-527. doi: 10.1111/cge.13077. Epub 2017 Sep 25.
Clin Genet. 2017.
PMID: 28632965
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
Voskarides K, Papagregoriou G, Hadjipanagi D, Petrou I, Savva I, Elia A, Athanasiou Y, Pastelli A, Kkolou M, Hadjigavriel M, Stavrou C, Pierides A, Deltas C.
Voskarides K, et al. Among authors: hadjipanagi d.
BMC Nephrol. 2018 May 16;19(1):114. doi: 10.1186/s12882-018-0906-5.
BMC Nephrol. 2018.
PMID: 29764427
Free PMC article.
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Evidence for contribution of the y chromosome in atherosclerotic plaque occurrence in men.
Voskarides K, Hadjipanagi D, Papazachariou L, Griffin M, Panayiotou AG.
Voskarides K, et al. Among authors: hadjipanagi d.
Genet Test Mol Biomarkers. 2014 Aug;18(8):552-6. doi: 10.1089/gtmb.2014.0020. Epub 2014 Apr 10.
Genet Test Mol Biomarkers. 2014.
PMID: 24720269
Clinical Trial.
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Genetic polymorphisms in warfarin and tacrolimus-related genes VKORC1, CYP2C9 and CYP3A5 in the Greek-Cypriot population.
Hadjipanagi D, Chrysanthou S, Voskarides K, Deltas C.
Hadjipanagi D, et al.
BMC Res Notes. 2014 Mar 5;7:123. doi: 10.1186/1756-0500-7-123.
BMC Res Notes. 2014.
PMID: 24593903
Free PMC article.
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Y-chromosome phylogeographic analysis of the Greek-Cypriot population reveals elements consistent with Neolithic and Bronze Age settlements.
Voskarides K, Mazières S, Hadjipanagi D, Di Cristofaro J, Ignatiou A, Stefanou C, King RJ, Underhill PA, Chiaroni J, Deltas C.
Voskarides K, et al. Among authors: hadjipanagi d.
Investig Genet. 2016 Feb 11;7:1. doi: 10.1186/s13323-016-0032-8. eCollection 2016.
Investig Genet. 2016.
PMID: 26870315
Free PMC article.
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Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife.
Żurowska AM, Bielska O, Daca-Roszak P, Jankowski M, Szczepańska M, Roszkowska-Bjanid D, Kuźma-Mroczkowska E, Pańczyk-Tomaszewska M, Moczulska A, Drożdż D, Hadjipanagi D, Deltas C, Ostalska-Nowicka D, Rabiega A, Taraszkiewicz J, Taranta-Janusz K, Wieczorkiewicz-Plaza A, Jobs K, Mews J, Musiał K, Jakubowska A, Nosek H, Jander AE, Koutsofti C, Stanisławska-Sachadyn A, Kuleszo D, Ziętkiewicz E, Lipska-Ziętkiewicz BS.
Żurowska AM, et al. Among authors: hadjipanagi d.
Kidney Int. 2021 Jun;99(6):1451-1458. doi: 10.1016/j.kint.2020.10.040. Epub 2020 Dec 10.
Kidney Int. 2021.
PMID: 33309955
Free article.
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Novel and Founder Pathogenic Variants in X-Linked Alport Syndrome Families in Greece.
Hadjipanagi D, Papagregoriou G, Koutsofti C, Polydorou C, Alivanis P, Andrikos A, Christodoulidou S, Dardamanis M, Diamantopoulos AA, Fountoglou A, Frangou E, Georgaki E, Giannikouris I, Gkinis V, Goudas PC, Kalaitzidis RG, Kaperonis N, Koutroumpas G, Makrydimas G, Myserlis G, Mitsioni A, Paliouras C, Papachristou F, Papadopoulou D, Papagalanis N, Papagianni A, Perysinaki G, Siomou E, Sombolos K, Tzanakis I, Vergoulas GV, Printza N, Deltas C.
Hadjipanagi D, et al.
Genes (Basel). 2022 Nov 24;13(12):2203. doi: 10.3390/genes13122203.
Genes (Basel). 2022.
PMID: 36553470
Free PMC article.
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