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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Renal graft outcome in autosomal dominant medullary cystic kidney disease type 1 von Soloukides, Andreas P, Moutzouris, Dimitrios-Anestis D, Papagregoriou, Gregory N, Stavrou, Christoforos V, Deltas, Constantinos C, Tzanatos, Helen A

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Increased Susceptibility and 9-Fold Increased Mortality From COVID-19 in Patients With ADTKD-MUC1: TH-PO380 von Kidd, Kendrah O., Vyletal, Petr, Kim, Alice, Taylor, Abbigail, Zivna, Martina, Stavrou, Christoforos, Conlon, Peter J., Hogan, Richard E., Papagregoriou, Gregory, Kmoch, Stanislav, Bleyer, Anthony J.

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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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An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes von Živná, Martina, Kidd, Kendrah, Zaidan, Mohamad, Vyleťal, Petr, Barešová, Veronika, Hodaňová, Kateřina, Sovová, Jana, Hartmannová, Hana, Votruba, Miroslav, Trešlová, Helena, Jedličková, Ivana, Sikora, Jakub, Hůlková, Helena, Robins, Victoria, Hnízda, Aleš, Živný, Jan, Papagregoriou, Gregory, Mesnard, Laurent, Beck, Bodo B., Wenzel, Andrea, Tory, Kálmán, Häeffner, Karsten, Wolf, Matthias T.F., Bleyer, Michael E., Sayer, John A., Ong, Albert C.M., Balogh, Lídia, Jakubowska, Anna, Łaszkiewicz, Agnieszka, Clissold, Rhian, Shaw-Smith, Charles, Munshi, Raj, Haws, Robert M., Izzi, Claudia, Capelli, Irene, Santostefano, Marisa, Graziano, Claudio, Scolari, Francesco, Sussman, Amy, Trachtman, Howard, Decramer, Stephane, Matignon, Marie, Grimbert, Philippe, Shoemaker, Lawrence R., Stavrou, Christoforos, Abdelwahed, Mayssa, Belghith, Neila, Sinclair, Matthew, Claes, Kathleen, Kopel, Tal, Moe, Sharon, Deltas, Constantinos, Knebelmann, Bertrand, Rampoldi, Luca, Kmoch, Stanislav, Bleyer, Anthony J.

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FO067ADTKD-MUC1 IN THE CYPRIOT POPULATION: GENOTYPING, DEEP-PHENOTYPING, BIOMARKER DISCOVERY AND THE SEARCH FOR A ROBUST TREATMENT von Papagregoriou, Gregory, Stavrou, Christoforos, Christofides, Andrea, Koutsofti, Constantina, Zivna, Martina, Kuhn, Eric, Roignot, Julie, Kmoch, Stanislav, Bleyer, Anthony J, Greka, Anna, Deltas, Constantinos

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An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes von Zivna, Martina, Kidd, Kendrah, Zaidan, Mohamad, Vyletal, Petr, Baresova, Veronika, Hodanova, Katerina, Sovova, Jana, Hartmannova, Hana, Votruba, Miroslav, Treslova, Helena, Jedlickova, Ivana, Sikora, Jakub, Hulkova, Helena, Robins, Victoria, Hnizda, Ales, Zivny, Jan, Papagregoriou, Gregory, Mesnard, Laurent, Beck, Bodo B, Wenzel, Andrea, Tory, Kalman, Haeeffner, Karsten, Wolf, Matthias T.F, Bleyer, Michael E, Sayer, John A, Ong, Albert C.M, Balogh, Lidia, Jakubowska, Anna, Laszkiewicz, Agnieszka, Clissold, Rhian, Shaw-Smith, Charles, Munshi, Raj, Haws, Robert M, Izzi, Claudia, Capelli, Irene, Santostefano, Marisa, Graziano, Claudio, Scolari, Francesco, Sussman, Amy, Trachtman, Howard, Decramer, Stephane, Matignon, Marie, Grimbert, Philippe, Shoemaker, Lawrence R, Stavrou, Christoforos, Abdelwahed, Mayssa, Belghith, Neila, Sinclair, Matthew, Claes, Kathleen, Kopel, Tal, Moe, Sharon, Deltas, Constantinos, Knebelmann, Bertrand, Rampoldi, Luca, Kmoch, Stanislav, Bleyer, Anthony J

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An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes von Živná, Martina, Kidd, Kendrah, Zaidan, Mohamad, Vyleťal, Petr, Barešová, Veronika, Hodaňová, Kateřina, Sovová, Jana, Hartmannová, Hana, Votruba, Miroslav, Trešlová, Helena, Jedličková, Ivana, Sikora, Jakub, Hůlková, Helena, Robins, Victoria, Hnízda, Aleš, Živný, Jan, Papagregoriou, Gregory, Mesnard, Laurent, Beck, Bodo B., Wenzel, Andrea, Tory, Kálmán, Häeffner, Karsten, Wolf, Matthias T.F., Bleyer, Michael E., Sayer, John A., Ong, Albert C.M., Balogh, Lídia, Jakubowska, Anna, Łaszkiewicz, Agnieszka, Clissold, Rhian, Shaw-Smith, Charles, Munshi, Raj, Haws, Robert M., Izzi, Claudia, Capelli, Irene, Santostefano, Marisa, Graziano, Claudio, Scolari, Francesco, Sussman, Amy, Trachtman, Howard, Decramer, Stephane, Matignon, Marie, Grimbert, Philippe, Shoemaker, Lawrence R., Stavrou, Christoforos, Abdelwahed, Mayssa, Belghith, Neila, Sinclair, Matthew, Claes, Kathleen, Kopel, Tal, Moe, Sharon, Deltas, Constantinos, Knebelmann, Bertrand, Rampoldi, Luca, Kmoch, Stanislav, Bleyer, Anthony J.

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Chromosome 1 Localization of a Gene for Autosomal Dominant Medullary Cystic Kidney Disease (ADMCKD) von Christodoulou, Kyproula, Tsingis, Marios, Stavrou, Christoforos, Eleftheriou, Andri, Papapavlou, Petros, Patsalis, Philippos C., Ioannou, Panos, Pierides, Alkis, Constantinou Deltas, C.

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Outcome of kidney transplantation in autosomal dominant medullary cystic kidney disease type 1 von Stavrou, Christoforos, Deltas, C. Constantinou, Christophides, Tasos C., Pierides, Alkis

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Autosomal dominant medullary cystic kidney disease : evidence of gene locus heterogeneity von FUCHSHUBER, A, CONSTANTINOU DELTAS, C, PIERIDES, A, HILDEBRANDT, F, BERTHOLD, S, STAVROU, C, VOLLMER, M, BURTON, C, FEEST, T, KRIETER, D, GAL, A, BRANDIS, M

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Novel NPR1 polymorphic variants and its exclusion as a candidate gene for medullary cystic kidney disease (ADMCKD) type 1 von Koptides, Michael, Mean, Richard, Stavrou, Christoforos, Pierides, Alkis, Demetriou, Kyproula, Nakayama, Tomohiro, Hildebrandt, Friedhelm, Fuchshuber, Arno, Deltas, C.Constantinou

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Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: No allelism with nephronophthisis type 1 von Stavrou, Christoforos, Pierides, Alkis, Zouvani, Ioanna, Kyriacou, Kyriacos, Antignac, Corinne, Neophytou, Pavlos, Christodoulou, Kyproula, Deltas, C. Constantinou

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COVID-19 Phenotypes and Comorbidity: A Data-Driven, Pattern Recognition Approach Using National Representative Data from the United States von Vavougios, George D, Stavrou, Vasileios T, Konstantatos, Christoforos, Sinigalias, Pavlos-Christoforos, Zarogiannis, Sotirios G, Kolomvatsos, Konstantinos, Stamoulis, George, Gourgoulianis, Konstantinos I

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Chiral Separation of the Clinically Important Compounds Fucose and Pipecolic Acid Using CE: Determination of the Most Effective Chiral Selector von Hadjistasi, Christoforos A., Stavrou, Ioannis J., Stefan-Van Staden, Raluca-Ioana, Aboul-Enein, Hassan Y., Kapnissi-Christodoulou, Constantina P.

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