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Journal of Electrocardiology|March 18, 2020
A novel variant of RyR2 gene in a family misdiagnosed as congenital long QT syndrome: The importance of genetic testingKonstantinos P Letsas, Efstathia Prappa, George Bazoukis, et al.Hellenic Journal of Nuclear Medicine|August 23, 2023
Transthyretin (Pro24Ser) variant amyloidosis: A case report of the first patient in GreeceIoannis Panagiotopoulos, Efstathios Papatheodorou, Aris Anastasakis, et al.BMC Medical Genetics|April 7, 2019
A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3)Malena P Pantou, Polyxeni Gourzi, Aggeliki Gkouziouta, et al.European Journal of Medical Genetics|May 14, 2018
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 diseasePolyxeni Gourzi, Malena P Pantou, Angeliki Gkouziouta, et al.Journal of Electrocardiology|February 24, 2021
KCNE2 gene mutation and Brugada syndromeIoannis Liatakis, Malena P Pantou, Polyxeni Gourzi, et al.American Journal of Cardiovascular Disease|July 29, 2021
RBM20 mutation and ventricular arrhythmias in a young patient with dilated cardiomyopathy: a case reportIoannis Liatakis, Efstathia Prappa, Aggeliki Gouziouta, et al.The Journal of Experimental Medicine|April 25, 2007
Regulation of AID expression in the immune responseElizabeth E Crouch, Zhiyu Li, Makiko Takizawa, et al.Pageof 2