RAAS inhibition and the course of Alport syndrome von Savva, Isavella, Pierides, Alkis, Deltas, Constantinos

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Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis von Gale, Daniel P, MRCP, de Jorge, Elena Goicoechea, PhD, Cook, H Terence, Prof, Martinez-Barricarte, Rubén, PhD, Hadjisavvas, Andreas, PhD, McLean, Adam G, FRCP, Pusey, Charles D, Prof, Pierides, Alkis, FRCP, Kyriacou, Kyriacos, PhD, Athanasiou, Yiannis, MD, Voskarides, Konstantinos, PhD, Deltas, Constantinos, Prof, Palmer, Andrew, FRCP, Frémeaux-Bacchi, Véronique, PhD, de Cordoba, Santiago Rodriguez, Prof, Maxwell, Patrick H, Prof, Pickering, Matthew C, Prof

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COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy von VOSKARIDES, Konstantinos, DAMIANOU, Loukas, PIERIDES, Alkis, KYRIACOU, Kyriacos, DELTAS, Constantinos, NEOCLEOUS, V Assos, ZOUVANI, Loanna, CHRISTODOULIDOU, Stalo, HADJICONSTANTINOU, Valsamakis, IOANNOU, Kyriacos, ATHANASIOU, Yiannis, PATSIAS, Charalampos, ALEXOPOULOS, Efstathios

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Familial C3 Glomerulopathy Associated with CFHR5 Mutations: Clinical Characteristics of 91 Patients in 16 Pedigrees von Athanasiou, Yiannis, Voskarides, Konstantinos, Gale, Daniel P, Damianou, Loukas, Patsias, Charalambos, Zavros, Michalis, Maxwell, Patrick H, Cook, H Terence, Demosthenous, Panayiota, Hadjisavvas, Andreas, Kyriacou, Kyriacos, Zouvani, Ioanna, Pierides, Alkis, Deltas, Constantinos

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COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect? von Voskarides, Konstantinos, Papagregoriou, Gregory, Hadjipanagi, Despina, Petrou, Ioanelli, Savva, Isavella, Elia, Avraam, Athanasiou, Yiannis, Pastelli, Androulla, Kkolou, Maria, Hadjigavriel, Michalis, Stavrou, Christoforos, Pierides, Alkis, Deltas, Constantinos

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Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental... von Papazachariou, Louiza, Demosthenous, Panayiota, Pieri, Myrtani, Papagregoriou, Gregory, Savva, Isavella, Stavrou, Christoforos, Zavros, Michael, Athanasiou, Yiannis, Ioannou, Kyriakos, Patsias, Charalambos, Panagides, Alexia, Potamitis, Costas, Demetriou, Kyproula, Prikis, Marios, Hadjigavriel, Michael, Kkolou, Maria, Loukaidou, Panayiota, Pastelli, Androulla, Michael, Aristos, Lazarou, Akis, Arsali, Maria, Damianou, Loukas, Goutziamani, Ioanna, Soloukides, Andreas, Yioukas, Lakis, Elia, Avraam, Zouvani, Ioanna, Polycarpou, Polycarpos, Pierides, Alkis, Voskarides, Konstantinos, Deltas, Constantinos

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A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general populati... von Voskarides, Konstantinos, Stefanou, Charalambos, Pieri, Myrtani, Demosthenous, Panayiota, Felekkis, Kyriakos, Arsali, Maria, Athanasiou, Yiannis, Xydakis, Dimitris, Stylianou, Kostas, Daphnis, Eugenios, Goulielmos, Giorgos, Loizou, Petros, Savige, Judith, Höhne, Martin, Völker, Linus A, Benzing, Thomas, Maxwell, Patrick H, Gale, Daniel P, Gorski, Mathias, Böger, Carsten, Kollerits, Barbara, Kronenberg, Florian, Paulweber, Bernhard, Zavros, Michalis, Pierides, Alkis, Deltas, Constantinos

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A miR-1207-5p binding site polymorphism abolishes regulation of HBEGF and is associated with disease severity in CFHR5 nephropathy von Papagregoriou, Gregory, Erguler, Kamil, Dweep, Harsh, Voskarides, Konstantinos, Koupepidou, Panayiota, Athanasiou, Yiannis, Pierides, Alkis, Gretz, Norbert, Felekkis, Kyriacos N, Deltas, Constantinos

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Genetic Variation of DKK3 May Modify Renal Disease Severity in ADPKD von LIU, Michelle, SHI, Sally, PIERIDES, Alkis, DEMETRIOU, Kyproula, DEVUYST, Olivier, GITOMER, Berenice, LAAKSO, Marku, LUMIAHO, Anne, LAMNISSOU, Klea, MAGISTRONI, Riccardo, PARFREY, Patrick, BREUNING, Martijn, SENTHILNATHAN, Sean, PETERS, Dorien J. M, TORRA, Roser, WINEARLS, Christopher G, TORRES, Vicente E, HARRIS, Peter C, PATERSON, Andrew D, PEI, York, YU, Julie, WU, Elliot, BERGMANN, Carsten, ZERRES, Klaus, BOGDANOVA, Nadja, COTO, Eliecer, DELTAS, Constantinos

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Epistatic role of the MYH9/APOL1 region on familial hematuria genes von Voskarides, Konstantinos, Demosthenous, Panayiota, Papazachariou, Louiza, Arsali, Maria, Athanasiou, Yiannis, Zavros, Michalis, Stylianou, Kostas, Xydakis, Dimitris, Daphnis, Eugenios, Gale, Daniel P, Maxwell, Patrick H, Elia, Avraam, Pattaro, Cristian, Pierides, Alkis, Deltas, Constantinos

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COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis von Deltas, Constantinos, Pierides, Alkis

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COL4A3/COL4A4 Mutations Link Familial Hematuria and Focal Segmental Glomerulosclerosis. Glomerular Epithelium Destruction via Basement Membrane Thinning? von Voskarides, Konstantinos, Pierides, Alkis, Deltas, Constantinos

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Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease von MAGISTRONI, Riccardo, NING HE, COTO, Eliecer, VAN DIJK, Marjan, BREUNING, Martijn, PETERS, Dorien, BOGDANOVA, Nadja, LIGABUE, Giulia, ALBERTAZZI, Alberto, HATEBOER, Nick, DEMETRIOU, Kyproula, PIERIDES, Alkis, WANG, Kairong, DELTAS, Constantinos, GEORGE-HYSLOP, Peter St, RAVINE, David, PEI, York, ANDREW, Robin, JOHNSON, Ann, GABOW, Patricia, DICKS, Elizabeth, PARFREY, Patrick, TORRA, Roser, SAN-MILLAN, Jose L

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Molecular genetics of familial hematuric diseases von Deltas, Constantinos, Pierides, Alkis, Voskarides, Konstantinos

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Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life von Deltas, Constantinos, Savva, Isavella, Voskarides, Konstantinos, Papazachariou, Louiza, Pierides, Alkis

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The role of molecular genetics in diagnosing familial hematuria(s) von Deltas, Constantinos, Pierides, Alkis, Voskarides, Konstantinos

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Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haemat... von Pierides, Alkis, Voskarides, Konstantinos, Athanasiou, Yiannis, Ioannou, Kyriacos, Damianou, Loukas, Arsali, Maria, Zavros, Michalis, Pierides, Michael, Vargemezis, Vasilios, Patsias, Charalambos, Zouvani, Ioanna, Elia, Avraam, Kyriacou, Kyriacos, Deltas, Constantinos

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Autosomal-dominant medullary cystic kidney disease type 1: Clinical and molecular findings in six large Cypriot families von Stavrou, Christoforos, Koptides, Michael, Tombazos, Christos, Psara, Evlalia, Patsias, Charalambos, Zouvani, Ioanna, Kyriacou, Kyriacos, Hildebrandt, Friedhelm, Christofides, Tasos, Pierides, Alkis, Deltas, C. Constantinou

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A family with the branchio‐oto‐renal syndrome: clinical and genetic correlations von Pierides, Alkis M., Athanasiou, Yiannis, Demetriou, Kyproula, Koptides, Michael, Deltas, C. Constantinou

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On ‘Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations’ von Voskarides, Konstantinos, Pierides, Alkis, Deltas, Constantinos

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