Neutrophil gelatinase-associated lipocalin (NGAL) in inflammatory bowel disease: association with pathophysiology of inflammation, established markers, and disease activity von Oikonomou, K. A., Kapsoritakis, A. N., Theodoridou, C., Karangelis, D., Germenis, A., Stefanidis, I., Potamianos, S. P.

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On the pathogenicity of the plasminogen K330E mutation for hereditary angioedema von Germenis, A. E., Loules, G., Zamanakou, M., Psarros, F., González‐Quevedo, T., Speletas, M., Bork, K., Wulff, K., Steinmüller‐Magin, L., Brænne, I., Staubach‐Renz, P., Witzke, G., Hardt, J.

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Rapid detection of MYD88-L265P mutation by PCR-RFLP in B-cell lymphoproliferative disorders von Argentou, N, Vassilopoulos, G, Ioannou, M, Germenis, A E, Speletas, M

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F12‐46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema von Speletas, M., Szilágyi, Á., Csuka, D., Koutsostathis, N., Psarros, F., Moldovan, D., Magerl, M., Kompoti, M., Varga, L., Maurer, M., Farkas, H., Germenis, A. E.

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Association between TLR2/TLR4 gene polymorphisms and COPD phenotype in a Greek cohort von Apostolou, A., Kerenidi, T., Michopoulos, A., Gourgoulianis, K. I., Noutsias, M., Germenis, A. E., Speletas, M.

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P0568 : TGF-β signaling is activated in patients with chronic hepatitis B and is repressed by SMAD 7 over expression during long term antiviral treatment von Germanidis, G, Argentou, N, Hytiroglou, P, Apostolou, E, Vassiliadis, T, Patsiaoura, K, Sideras, P, Germenis, A, Speletas, M

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Immunoepigenetics: the unseen side of cancer immunoediting von Germenis, A E, Karanikas, V

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Mitigating Disparity in Health-care Resources Between Countries for Management of Hereditary Angioedema von Jindal, Ankur Kumar, Reshef, Avner, Longhurst, Hilary

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Breast Cancer Risk in Relation to Most Prevalent IgE Specific Antibodies: A Case Control Study in Greece von PETRIDOU, E. T, CHAVELAS, C, DIKALIOTI, S. K, DESSYPRIS, N, TERZIDIS, A, NIKOULIS, D. I, MARKOPOULOS, C, PAPADIAMANTIS, Y, GERMENIS, A. E

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TLR4 single nucleotide polymorphisms and thrombosis risk in patients with myeloproliferative disorders von Speletas, M, Liadaki, K, Kalala, F, Daiou, C, Katodritou, E, Mandala, E, Korantzis, I, Ritis, K, Zintzaras, E, Germenis, A.E

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Morning levels of fibrinogen in children with sleep-disordered breathing von Kaditis, A.G, Alexopoulos, E.I, Kalampouka, E, Kostadima, E, Angelopoulos, N, Germenis, A, Zintzaras, E, Gourgoulianis, K

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DHLAS: A web-based information system for statistical genetic analysis of HLA population data von Thriskos, P, Zintzaras, E, Germenis, A

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International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency von Farkas, H., Martinez‐Saguer, I., Bork, K., Bowen, T., Craig, T., Frank, M., Germenis, A. E., Grumach, A. S., Luczay, A., Varga, L., Zanichelli, A., Aberer, Werner, Andrejevic, Sladjana, Aygoeren‐Pürsün, Emel, Banerji, Alena, Bara, Noemi‐Anna, Bas, Murat, Bernstein, Jonathan, Betschel, Stephen, Björkander, Janne, Boccon‐Gibod, Isabelle, Bouillet, Laurence, Bova, Maria, Boysen, Henrik Halle, Branco‐Ferreira, Manuel, Bygum, Anette, Caballero, Teresa, Cancian, Mauro, Castaldo, Anthony, Christiansen, Sandra, Cicardi, Marco, Drouet, Christian, Fabiani, Jose, Gompels, Mark, Gonzalez‐Quevedo, Maria Teresa, Gooi, Jimmy, Gower, Richard, Gökmen, Nihal Mete, Grivcheva‐Panovska, Vesna, Guilarte, Mar, Gülbahar, Okan, Hack, Erik, Hakl, Roman, Harmat, György, Jeseňák, Miloš, Jolles, Stephen, Kaplan, Allen, Katelaris, Connie, Kosnik, Mitja, Kőhalmi, Kinga Viktória, Leibovich, Iris, Levi, Marcel, Li, Henry, Longhurst, Hilary J., Lumry, William, Magerl, Markus, Malbran, Alejandro, Martin, Ludovic, Maurer, Marcus, Mihály, Enikő, Moldovan, Dumitru, Murdjeva, Mariana, Nagy, Imola Beatrix, Nielsen, Erik W., Nieto, Sandra, Nordenfelt, Patrik, Obtulowitzc, Kristine, Pedrosa, Maria, Porębski, Grzegorz, Prior, Nieves, Reshef, Avner, Riedl, Marc A., Rosenkranz, Bernd, Schmid‐Grendelmeier, Peter, Péter, Spath, Speletas, Matthaios, Staevska, Maria, Stobiecki, Marcin, Triggiani, Massimo, Veszeli, Nóra, Wuillemin, Walter, Xiang, Zhi Yu, Yamamoto, Beverley, Zuraw, Bruce

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Foxp3 Expression in Liver Correlates with the Degree but Not the Cause of Inflammation von Speletas, Matthaios, Argentou, Nikoletta, Germanidis, Georgios, Vasiliadis, Themistoclis, Mantzoukis, Konstantinos, Patsiaoura, Kalliopi, Nikolaidis, Pavlos, Karanikas, Vaios, Ritis, Konstantinos, Germenis, Anastasios E.

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Tumor immune escape mediated by indoleamine 2,3-dioxygenase von Zamanakou, Maria, Germenis, Anastasios E, Karanikas, Vaios

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Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene von Daiou, C., Christodoulou, K., Xiromerisiou, G., Panas, M., Dardiotis, E., Kladi, A., Speletas, M., Ntaios, G., Papadimitriou, A., Germenis, A., Hadjigeorgiou, Georgios M.

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Association of TLR4-T399I Polymorphism with Chronic Obstructive Pulmonary Disease in Smokers von Merentiti, Vassiliki, Liadaki, Kyriaki, Speletas, Matthaios, Germenis, Anastasios E., Gourgoulianis, K. I., Minas, Markos, Kostikas, Konstantinos

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International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency von Farkas, H, Martinez-Saguer, I, Bork, K, Bowen, T, Craig, T, Frank, M, Germenis, A E, Grumach, A S, Luczay, A, Varga, L, Zanichelli, A

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Morning Levels of C-Reactive Protein in Children with Obstructive Sleep-disordered Breathing von Kaditis, Athanasios G, Alexopoulos, Emmanouel I, Kalampouka, Efthimia, Kostadima, Eleni, Germenis, Anastasios, Zintzaras, Elias, Gourgoulianis, Konstantinos

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Soluble adhesion molecules are not involved in the development of retinopathy in type 2 diabetic patients von Boulbou, M S, Koukoulis, G N, Petinaki, E A, Germenis, A, Gourgoulianis, K I

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