Phenotypic variability and molecular genetics in proximal myotonic myopathy von Papadimas, George Konstantinos, Kekou, Kiriaki, Papadopoulos, Constantinos, Kararizou, Evangelia, Kanavakis, Emmanuel, Manta, Panagiota

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The genetic etiology in cerebral palsy mimics: The results from a Greek tertiary care center von Zouvelou, Vasiliki, Yubero, Delia, Apostolakopoulou, Loukia, Kokkinou, Eleftheria, Bilanakis, Manolis, Dalivigka, Zoi, Nikas, Ioannis, Kollia, Elissavet, Perez-Dueñas, Belen, Macaya, Alfons, Marcé-Grau, Anna, Voutetakis, Antonis, Anagnostopoulou, Katerina, Kekou, Kiriaki, Sofocleus, Christalena, Veltra, Danae, Kokkinis, Xaralabos, Fryssira, Helen, Torres, Rosa J., Amstrong, Judith, Santorelli, Filippo M., Artuch, Rafael, Pons, Roser

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Association of VEGF Gene Polymorphisms with the Development of Heart Failure in Patients after Myocardial Infarction von Douvaras, Panagiotis, Antonatos, Dionisios G., Kekou, Kiriaki, Patsilinakos, Sotirios, Chouliaras, George, Christou, Apostolos, Andrikou, Anastasios, Kanavakis, Emmanuel

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Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol von Kekou, Kiriaki, Fryssira, Helena, Sophocleous, Christalena, Mavrou, Ariadni, Manta, Panagiota, Metaxotou, Catherine

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Deletion patterns of Duchenne and Becker muscular dystrophies in Greece von Florentin, L, Mavrou, A, Kekou, K, Metaxotou, C

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3′ acceptor splice site mutation in intron 50 leads to mild duchenne muscular dystrophy phenotype von Kekou, Kiriaki, Florentin, Lina, Metaxotou, Catherine

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