Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome

Electroanatomical voltage mapping with contact force sensing for diagnosis of arrhythmogenic right ventricular cardiomyopathy.

International journal of cardiology·2023

Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemia.

Bratislavske lekarske listy·2018

Multiple clinical profiles of families with the short QT syndrome.

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology·2017

Hemoglobin Lepore Boston in a Turkish Family.

Turkish journal of haematology : official journal of Turkish Society of Haematology·2016

Multiple Cerebral Emboli in a Homozygous b-Thalassaemia Patient Due to Factor V 1299 (His-Arg) 4070 A-G Mutation.

Turkish journal of haematology : official journal of Turkish Society of Haematology·2016