Pneumothorax Complicating Bullous Emphysema in Childhood Tuberculosis von Karpouzas, J., Papagregoriou, M.

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Relationship between tocopherols and serum lipid levels in children with beta-thalassemia major von Zannos-Mariolea, L, Papagregoriou-Theodoridou, M, Costantzas, N, Matsaniotis, N

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biobank.cy: the Biobank of Cyprus past, present and future von Loizidou, Eleni M., Kyratzi, Maria, Tsiarli, Maria A., Kakouri, Andrea C., Charalambidou, Georgia, Antoniou, Stella, Pieri, Stylianos, Veloudi, Panagiota, Mayrhofer, Michaela Th, Wutte, Andrea, Kozera, Lukasz, Habermann, Jens, Muller, Heimo, Zatloukal, Kurt, Sargsyan, Karine, Michaelides, Alexandros, Papaioannou, Maria, Schizas, Christos, Malatras, Apostolos, Papagregoriou, Gregory, Deltas, Constantinos

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Risk mapping for better governance in biobanking: the case of biobank.cy von Akyüz, Kaya, Goisauf, Melanie, Martin, Gillian M, Mayrhofer, Michaela Th, Antoniou, Stella, Charalambidou, Georgia, Deltas, Constantinos, Malatras, Apostolos, Papagregoriou, Gregory, Stefanou, Charalambos, Voutounou, Mariel

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Relationship between tocopherols and serum lipid levels in children with β-thalassemia major1 von Zannos-Mariolea, L, Papagregoriou-Theodoridou, M, Costantzas, N, Matsaniotis, N

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Detection of profilin in SPT extracts that are supposed to contain it von Pitsios, C, Iliopoulou, A, Kontogianni, M, Papagregoriou, G

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Relationship between tocophercols and serum lipid levels in children with beta thalassemia major von Zannos-Mariolea, L, Papagregoriou-Theodoridou, M, Costantzas, N, Matsaniotis, N

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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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biobank.cy: the Biobank of Cyprus past, present and 0 future von Loizidou, Eleni M, Kyratzi, Maria, Tsiarli, Maria A, Kakouri, Andrea C, Charalambidou, Georgia, Antoniou, Stella, Pieri, Stylianos, Veloudi, Panagiota, Mayrhofer, Michaela Th, Wutte, Andrea, Kozera, Lukasz, Habermann, Jens, Muller, Heimo, Zatloukal, Kurt, Sargsyan, Karine, Michaelides, Alexandros, Papaioannou, Maria, Schizas, Christos, Malatras, Apostolos, Papagregoriou, Gregory, Deltas, Constantinos

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FIRST-IN-HUMAN PHASE I/II CLINICAL TRIAL OF IG-TREGS FOR GVHD PREVENTION von Lysandrou, M., Kefala, D., Christofi, P., Liga, M., Miggos, A., Papagregoriou, C., Vlachonikola, E., Savvopoulos, N., Zacharioudaki, V., Vallianou, I., Sagiadinou, E., Tsokanas, D., Theodorelou, R., Papadopoulou, A., Triantafyllou, E., Sakellari, I., Costeas, P., Chatzidimitriou, A., Yannaki, E., Spyridonidis, A.

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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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LILRB3 (ILT5) is a myeloid cell checkpoint that elicits profound immunomodulation von Yeboah, Muchaala, Papagregoriou, Charys, Jones, Des C, Chan, H T Claude, Hu, Guangan, McPartlan, Justine S, Schiött, Torbjörn, Mattson, Ulrika, Mockridge, C Ian, Tornberg, Ulla-Carin, Hambe, Björn, Ljungars, Anne, Mattsson, Mikael, Tews, Ivo, Glennie, Martin J, Thirdborough, Stephen M, Trowsdale, John, Frendeus, Björn, Chen, Jianzhu, Cragg, Mark S, Roghanian, Ali

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Neuroprotective effects of EPA and DHA fatty acids in the DBA/2J hereditary glaucoma mouse model von Kalogerou, M., Prokopiou, K., Kolovos, P., Malas, S., Papagregoriou, G., Deltas, C., Georgiou, T.

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76P Monitoring pembrolizumab response in patients with metastatic non-small cell lung cancer using circulating tumour DNA and circulating tumour cells von Kakouri, A.C., Spiliotaki, M., Loizidou, E.M., Stylianou, I., Papageorgiou, E., Panayi, C.G., Constantinou, A.I., Charalambous, H.C., Deltas, C., Papagregoriou, G.

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Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease von Živná, Martina, Kidd, Kendrah, Přistoupilová, Anna, Barešová, Veronika, DeFelice, Mathew, Blumenstiel, Brendan, Harden, Maegan, Conlon, Peter, Lavin, Peter, Connaughton, Dervla M, Hartmannová, Hana, Hodaňová, Kateřina, Stránecký, Viktor, Vrbacká, Alena, Vyleťal, Petr, Živný, Jan, Votruba, Miroslav, Sovová, Jana, Hůlková, Helena, Robins, Victoria, Perry, Rebecca, Wenzel, Andrea, Beck, Bodo B, Seeman, Tomáš, Viklický, Ondřej, Rajnochová-Bloudíčková, Sylvie, Papagregoriou, Gregory, Deltas, Constantinos C, Alper, Seth L, Greka, Anna, Bleyer, Anthony J, Kmoch, Stanislav

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Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1 von Olinger, E, Hofmann, P, Kidd, K, Dufour, I, Belge, H, Schaeffer, C, Kipp, A, Bonny, O, Deltas, C, Demoulin, N, Fehr, T, Fuster, D G, Gale, D P, Goffin, E, Hodanova, K, Huynh-Do, Uyen, Kistler, Andreas, Morelle, J, Papagregoriou, G, Pirson, Y, Sandford, R, Sayer, J A, Torra, R, Venzin, C, Venzin, R, Vogt, B, Živná, M, Greka, A, Dahan, K, Rampoldi, L, Devuyst, Olivier

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Massive Parallel DNA Sequencing of Patients with Inherited Cardiomyopathies in Cyprus and Suggestion of Digenic or Oligogenic Inheritance von Koutsofti, Constantina, Ioannides, Marios, Polydorou, Christiana, Papagregoriou, Gregory, Malatras, Apostolos, Michael, George, Hadjiioannou, Irene, Pieri, Stylianos, Loizidou, Eleni M, Eftychiou, Christos, Papasavvas, Elias, Christophides, Theodoros, Alkelai, Anna, Kapoor, Manav, Shuldiner, Alan R, Avraamides, Panayiotis, 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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X-linked Alport syndrome in Hellenic families: Phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5 von Demosthenous, P, Voskarides, K, Stylianou, K, Hadjigavriel, M, Arsali, M, Patsias, C, Georgaki, E, Zirogiannis, P, Stavrou, C, Daphnis, E, Pierides, A, Deltas, C

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LILRB3 (ILT5) is a myeloid cell checkpoint that elicits profound immunomodulation von Yeboah, Muchaala, Papagregoriou, Charys, Jones, Des C, Chan, HT Claude, Hu, Guangan, McPartlan, Justine S, Schiött, Torbjörn, Mattson, Ulrika, Mockridge, C Ian, Tornberg, Ulla-Carin, Hambe, Björn, Ljungars, Anne, Mattsson, Mikael, Tews, Ivo, Glennie, Martin J, Thirdborough, Stephen M, Trowsdale, John, Frendeus, Björn, Chen, Jianzhu, Cragg, Mark S, Roghanian, Ali

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