An anthropometric-based method for the assessment of pelvis position in three-dimensional space von Mandalidis, D., Glakousakis, G., Kalatzis, P.

Volltext

Electrochemical degradation of Reactive Red 120 using DSA and BDD anodes von Panakoulias, T., Kalatzis, P., Kalderis, D., Katsaounis, A.

Volltext

T1.11 The management of 100 humeral shaft fractures with “Garnavos” humeral nail von Garnavos, C, Kakavas, P, Lasanianos, N, Priftis, A, Doudoulakis, K, Kalatzis, P, Boudouris, P

Volltext

Sa1.5 Techniques for closed reduction of irreducible inter and sub-trochanteric fractures von Garnavos, C, Kakavas, P, Priftis, A, Doudoulakis, K, Sarafopoulos, S, Kalatzis, P, Protopapadakis, G

Volltext

A27 Compression bolts at the distal side of the knee von Lasanianos, N, Sinnis, G, Protopapadakis, G, Kalatzis, P, Nikas, E

Volltext

Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles von Sanjurjo-Soriano, Carla, Erkilic, Nejla, Baux, David, Mamaeva, Daria, Hamel, Christian P., Meunier, Isabelle, Roux, Anne-Françoise, Kalatzis, Vasiliki

Volltext

Shedding Light on Colorectal Cancer: An In Vivo Raman Spectroscopy Approach Combined with Deep Learning Analysis von Kouri, Maria Anthi, Karnachoriti, Maria, Spyratou, Ellas, Orfanoudakis, Spyros, Kalatzis, Dimitris, Kontos, Athanassios G, Seimenis, Ioannis, Efstathopoulos, Efstathios P, Tsaroucha, Alexandra, Lambropoulou, Maria

Volltext

Medical data quality assessment: On the development of an automated framework for medical data curation von Pezoulas, Vasileios C., Kourou, Konstantina D., Kalatzis, Fanis, Exarchos, Themis P., Venetsanopoulou, Aliki, Zampeli, Evi, Gandolfo, Saviana, Skopouli, Fotini, De Vita, Salvatore, Tzioufas, Athanasios G., Fotiadis, Dimitrios I.

Volltext

Complementary DNA Microarray Image Processing Based on the Fuzzy Gaussian Mixture Model von Athanasiadis, E.I., Cavouras, D.A., Spyridonos, P.P., Glotsos, D.T., Kalatzis, I.K., Nikiforidis, G.C.

Volltext

Clinical Evaluation and Cone Alterations in Choroideremia von Nabholz, Nicolas, MD, Lorenzini, Marie-Céline, MSc, Bocquet, Béatrice, PhD, Lacroux, Annie, MSc, Faugère, Valérie, MSc, Roux, Anne-Françoise, PhD, Kalatzis, Vasiliki, PhD, Meunier, Isabelle, MD, PhD, Hamel, Christian P., MD, PhD

Volltext

Pathogenicity of a novel missense variant associated with choroideremia and its impact on gene replacement therapy von Torriano, Simona, Erkilic, Nejla, Faugère, Valérie, Damodar, Krishna, Hamel, Christian P, Roux, Anne-Francoise, Kalatzis, Vasiliki

Volltext

Advanced Raman Spectroscopy Based on Transfer Learning by Using a Convolutional Neural Network for Personalized Colorectal Cancer Diagnosis von Kalatzis, Dimitris, Spyratou, Ellas, Karnachoriti, Maria, Kouri, Maria Anthi, Orfanoudakis, Spyros, Koufopoulos, Nektarios, Pouliakis, Abraham, Danias, Nikolaos, Seimenis, Ioannis, Kontos, Athanassios G., Efstathopoulos, Efstathios P.

Volltext

Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis von Erkilic, Nejla, Sanjurjo-Soriano, Carla, Manes, Gaël, Dubois, Gregor, Hamel, Christian P., Meunier, Isabelle, Kalatzis, Vasiliki

Volltext

Enhancing medical data quality through data curation: a case study in primary Sjögren's syndrome von Pezoulas, Vasileios C, Kourou, Konstantina D, Kalatzis, Fanis, Exarchos, Themis P, Venetsanopoulou, Aliki I, Zampeli, Evi, Gandolfo, Saviana, Skopouli, Fotini N, De Vita, Salvatore, Tzioufas, Athanasios G, Fotiadis, Dimitrios I

Volltext

Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy von Erkilic, Nejla, Sanjurjo-Soriano, Carla, Diakatou, Michalitsa, Manes, Gaël, Dubois, Gregor, Hamel, Christian P., Meunier, Isabelle, Kalatzis, Vasiliki

Volltext

Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa von Sanjurjo-Soriano, Carla, Erkilic, Nejla, Manes, Gaël, Dubois, Gregor, Hamel, Christian P., Meunier, Isabelle, Kalatzis, Vasiliki

Volltext

Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2 von Sanjurjo-Soriano, Carla, Erkilic, Nejla, Manes, Gaël, Dubois, Gregor, Hamel, Christian P., Meunier, Isabelle, Kalatzis, Vasiliki

Volltext

The cell adhesion molecule "CAR" and sialic acid on human erythrocytes influence adenovirus in vivo biodistribution von Seiradake, Elena, Henaff, Daniel, Wodrich, Harald, Billet, Olivier, Perreau, Matthieu, Hippert, Claire, Mennechet, Franck, Schoehn, Guy, Lortat-Jacob, Hugues, Dreja, Hanna, Ibanes, Sandy, Kalatzis, Vasiliki, Wang, Jennifer P, Finberg, Robert W, Cusack, Stephen, Kremer, Eric J

Volltext

Extended Analysis of Raman Spectra Using Artificial Intelligence Techniques for Colorectal Abnormality Classification von Kalatzis, Dimitris, Spyratou, Ellas, Karnachoriti, Maria, Kouri, Maria Anthi, Stathopoulos, Ioannis, Danias, Nikolaos, Arkadopoulos, Nikolaos, Orfanoudakis, Spyros, Seimenis, Ioannis, Kontos, Athanassios G, Efstathopoulos, Efstathios P

Volltext

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family von Cruaud, Corinne, Leibovici, Michel, Compain, Sylvie, Lacombe, Didier, Bitner-Glindzicz, Maria, Vigneron, Jacqueline, Boven, Katia, Petit, Christine, Charachon, Robert, Francis, Mary, Weil, Dominique, Regemorter, Nicole Van, Samson, Delphine, Weissenbach, Jean, Bedbeder, Philippe, Heilig, Roland, Sahly, Iman, Abdelhak, Sonia, Kalatzis, Vasiliki, Vincent, Christophe

Volltext