A truncating variant altering the extreme C-terminal region of desmoplakin (DSP) suggests the crucial functional role of the region: a case report study von Pantou, Malena P, Gourzi, Polyxeni, Vlagkouli, Vasiliki, Papatheodorou, Efstathios, Tsoutsinos, Alexandros, Nyktari, Eva, Degiannis, Dimitrios, Anastasakis, Aris

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A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3) von Pantou, Malena P, Gourzi, Polyxeni, Gkouziouta, Aggeliki, Armenis, Iakovos, Kaklamanis, Loukas, Zygouri, Christianna, Constantoulakis, Pantelis, Adamopoulos, Stamatis, Degiannis, Dimitrios

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Phenotypic Heterogeneity within Members of a Family Carrying the Same RBM20 Mutation R634W von Pantou, Malena P., Gourzi, Polyxeni, Gkouziouta, Aggeliki, Tsiapras, Dimitrios, Zygouri, Christianna, Constantoulakis, Pantelis, Adamopoulos, Stamatis, Degiannis, Dimitrios

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The potential presence of the highly similar paralogue gene KCNE1B blurs the genetic basis of KCNE1-LQTS patients von Pantou, Malena P, Gourzi, Polyxeni, Degiannis, Dimitrios

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Connective tissue growth factor (CTGF/CCN2): A protagonist in cardiac allograft vasculopathy development? von Pantou, Malena P., PhD, Manginas, Athanasios, MD, Alivizatos, Peter A., MD, Degiannis, Dimitrios, MD, PhD

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A novel variant of RyR2 gene in a family misdiagnosed as congenital long QT syndrome: The importance of genetic testing von Letsas, Konstantinos P., Prappa, Efstathia, Bazoukis, George, Lioni, Louiza, Pantou, Malena P., Gourzi, Polyxeni, Degiannis, Dimitrios, Sideris, Antonios

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KCNE2 gene mutation and Brugada syndrome von Liatakis, Ioannis, Pantou, Malena P., Gourzi, Polyxeni, Bazoukis, George, Mililis, Panagiotis, Saplaouras, Athanasios, Vlachos, Konstantinos, Prappa, Efstathia, Degiannis, Dimitrios, Efremidis, Michael, Letsas, Konstantinos P.

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A new phenotype of severe dilated cardiomyopathy associated with a mutation in the LAMP2 gene previously known to cause hypertrophic cardiomyopathy in the context of Danon disease von Gourzi, Polyxeni, Pantou, Malena P., Gkouziouta, Angeliki, Kaklamanis, Loukas, Tsiapras, Dimitrios, Zygouri, Christianna, Constantoulakis, Pantelis, Adamopoulos, Stamatis, Degiannis, Dimitrios

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The complete mitochondrial genome of Fusarium oxysporum: Insights into fungal mitochondrial evolution von Pantou, Malena P., Kouvelis, Vassili N., Typas, Milton A.

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The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study von Karmiris, Efthymios, Kourtis, Nikos, P Pantou, Malena, Degiannis, Dimitris, Georgalas, Ilias, Papaconstantinou, Dimitrios

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complete mitochondrial genome of the vascular wilt fungus Verticillium dahliae: a novel gene order for Verticillium and a diagnostic tool for species identification von Pantou, M.P, Kouvelis, V.N, Typas, M.A

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Caspase 9 promoter polymorphisms confer increased susceptibility to breast cancer von Theodoropoulos, George E, Michalopoulos, Nikolaos V, Pantou, Malena P, Kontogianni, Panagiota, Gazouli, Maria, Karantanos, Theodoros, Lymperi, Maria, Zografos, George C

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IGS sequence variation, group-I introns and the complete nuclear ribosomal DNA of the entomopathogenic fungus Metarhizium: excellent tools for isolate detection and phylogenetic an... von Pantou, Malena P., Mavridou, Annoula, Typas, Milton A.

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Electrophoretic karyotype and gene mapping of the vascular wilt fungus Verticillium dahliae von Pantou, Malena P., Typas, Milton A.

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RBM20 mutation and ventricular arrhythmias in a young patient with dilated cardiomyopathy: a case report von Liatakis, Ioannis, Prappa, Efstathia, Gouziouta, Aggeliki, Pantou, Malena P, Gourzi, Polyxeni, Vlachos, Konstantinos, Mililis, Panagiotis, Kariki, Ourania, Degiannis, Dimitrios, Efremidis, Michael, Letsas, Konstantinos P

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Molecular and immunochemical phylogeny of Verticillium species von PANTOU, Malena P., STRUNNIKOVA, Olga K., SHAKHNAZAROVA, Vlada Yu, VISHNEVSKAYA, Nadezhda A., PAPALOUKA, Vasiliki G., TYPAS, Milton A.

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RBM20 mutation and ventricular arrhythmias in a young patient with dilated cardiomyopathy: a case report von Liatakis, Ioannis, Prappa, Efstathia, Gouziouta, Aggeliki, Pantou, Malena P, Gourzi, Polyxeni, Vlachos, Konstantinos, Mililis, Panagiotis, Kariki, Ourania, Degiannis, Dimitrios, Efremidis, Michael, Letsas, Konstantinos P

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A new phenotype of severe dilated cardiomyopathy associated with a mutation in the LAMP2 gene previously known to cause hypertrophic cardiomyopathy in the context of Danon disease von Gourzi, Polyxeni, Pantou, Malena P, Gkouziouta, Angeliki, Kaklamanis, Loukas, Tsiapras, Dimitrios, Zygouri, Christianna, Constantoulakis, Pantelis, Adamopoulos, Stamatis, Degiannis, Dimitrios

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