The Association between TGF-β1 G915C (Arg25Pro) Polymorphism and the Development of Primary Open Angle Glaucoma: A Case-Control Study

por KARMIRIS, Efthymios, KOURTIS, Nikos, P. PANTOU, Malena, DEGIANNIS, Dimitris, GEORGALAS, Ilias, PAPACONSTANTINOU, Dimitrios
Publicado 2018

Holt-Oram Syndrome in a Patient with Crohn’s Disease: a Rare Case Report and Literature Review

por Arkoumanis, Panagiotis-Theofanis, Gklavas, Antonios, Karageorgou, Margarita, Gourzi, Polyxeni, Mantzaris, Gerassimos, Pantou, Malena, Papaconstantinou, Ioannis
Publicado 2018

A truncating variant altering the extreme C-terminal region of desmoplakin (DSP) suggests the crucial functional role of the region: a case report study

por Pantou, Malena P., Gourzi, Polyxeni, Vlagkouli, Vasiliki, Papatheodorou, Efstathios, Tsoutsinos, Alexandros, Nyktari, Eva, Degiannis, Dimitrios, Anastasakis, Aris
Publicado 2023

A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3)

por Pantou, Malena P., Gourzi, Polyxeni, Gkouziouta, Aggeliki, Armenis, Iakovos, Kaklamanis, Loukas, Zygouri, Christianna, Constantoulakis, Pantelis, Adamopoulos, Stamatis, Degiannis, Dimitrios
Publicado 2019