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Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.
Papazachariou L, Papagregoriou G, Hadjipanagi D, Demosthenous P, Voskarides K, Koutsofti C, Stylianou K, Ioannou P, Xydakis D, Tzanakis I, Papadaki A, Kallivretakis N, Nikolakakis N, Perysinaki G, Gale DP, Diamantopoulos A, Goudas P, Goumenos D, Soloukides A, Boletis I, Melexopoulou C, Georgaki E, Frysira E, Komianou F, Grekas D, Paliouras C, Alivanis P, Vergoulas G, Pierides A, Daphnis E, Deltas C. Papazachariou L, et al. Among authors: vergoulas g. Clin Genet. 2017 Nov;92(5):517-527. doi: 10.1111/cge.13077. Epub 2017 Sep 25. Clin Genet. 2017. PMID: 28632965
Cardio-renal anemia syndrome.
Efstratiadis G, Konstantinou D, Chytas I, Vergoulas G. Efstratiadis G, et al. Among authors: vergoulas g. Hippokratia. 2008 Jan;12(1):11-6. Hippokratia. 2008. PMID: 18923761 Free PMC article.
Renal fibrosis.
Efstratiadis G, Divani M, Katsioulis E, Vergoulas G. Efstratiadis G, et al. Among authors: vergoulas g. Hippokratia. 2009 Oct;13(4):224-9. Hippokratia. 2009. PMID: 20011086 Free PMC article.
Rhabdomyolysis updated.
Efstratiadis G, Voulgaridou A, Nikiforou D, Kyventidis A, Kourkouni E, Vergoulas G. Efstratiadis G, et al. Among authors: vergoulas g. Hippokratia. 2007 Jul;11(3):129-37. Hippokratia. 2007. PMID: 19582207 Free PMC article.
26 results