Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek Patients by Ivantsik, Ouliana, John, Anne, Kydonopoulou, Kyriaki, Mitropoulos, Konstantinos, Gerou, Spyridon, Ali, Bassam R, Patrinos, George P

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Association of plasminogen activator inhibitor-type 1 (PAI-1) -675 4G/5G polymorphism with unexplained female infertility by Kydonopoulou, K, Delkos, D, Rousso, D, Ilonidis, G, Mandala, E

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Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients by Stratopoulos, Apostolos, Kolliopoulou, Alexandra, Karamperis, Kariofyllis, John, Anne, Kydonopoulou, Kyriaki, Esftathiou, George, Sgourou, Argyro, Kourakli, Alexandra, Vlachaki, Efthimia, Chalkia, Panagiota, Theodoridou, Stamatia, Papadakis, Manoussos N, Gerou, Spyridon, Symeonidis, Argiris, Katsila, Theodora, Ali, Bassam R, Papachatzopoulou, Adamantia, Patrinos, George P

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Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients by Mitropoulos, Konstantinos, Merkouri Papadima, Eleni, Xiromerisiou, Georgia, Balasopoulou, Angeliki, Charalampidou, Kyriaki, Galani, Vasiliki, Zafeiri, Krystallia-Vassiliki, Dardiotis, Efthymios, Ralli, Styliani, Deretzi, Georgia, John, Anne, Kydonopoulou, Kyriaki, Papadopoulou, Elpida, di Pardo, Alba, Akcimen, Fulya, Loizedda, Annalisa, Dobričić, Valerija, Novaković, Ivana, Kostić, Vladimir S, Mizzi, Clint, Peters, Brock A, Basak, Nazli, Orrù, Sandro, Kiskinis, Evangelos, Cooper, David N, Gerou, Spyridon, Drmanac, Radoje, Bartsakoulia, Marina, Tsermpini, Evangelia-Eirini, Hadjigeorgiou, Georgios M, Ali, Bassam R, Katsila, Theodora, Patrinos, George P

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