List of works - Elena V. Zaklyazminskaya

A Modern Approach to Classify Missense Mutations in Cardiac Channelopathy Genes ⬇️

scientific article published on 01 October 2012

Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy

scientific article published on 15 July 2020

Calmodulin binds to the N-terminal domain of the cardiac sodium channel Nav1.5.

scientific article published on 01 December 2020

Cardiac channelopathies: Genetic and molecular mechanisms ⬇️

scientific article published on December 22, 2012

Complex genetic background in a large family with Brugada syndrome

scientific article

Different Phenotypes of Sarcomeric MyBPC3-Cardiomyopathy in the Same Family: Hypertrophic, Left Ventricular Noncompaction and Restrictive Phenotypes (in Association with Sarcoidosis)

scientific article published in 2022

Laminopathies in Russian families.

scientific article published on 28 June 2008

Left ventricular noncompaction: A clinical and morphological study

scientific article

Myocardial Biopsy In "Idiopathic» Atrial Fibrillation And Other Arrhythmias: Nosological Diagnosis, Clinical And Morphological Parallels, And Treatment.

scientific article published on 30 June 2016

New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy

scientific article published on 4 October 2016

Prevalence of Significant Genetic Variants in Congenital Long QT Syndrome is Largely Underestimated ⬇️

scientific article published on April 27, 2012

Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics

scientific article published on 28 January 2012

The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.

scientific article

The role of mutations in the SCN5A gene in cardiomyopathies.

scientific article published on 22 February 2016

The use of noninvasive ECG imaging for examination of a patient with Brugada syndrome.

scientific article

[Eosinophilic granuloma of the parietal bone of an adult patient with BRAF mutation].

scientific article

List of works by Elena V. Zaklyazminskaya

A Modern Approach to Classify Missense Mutations in Cardiac Channelopathy Genes ⬇️

Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy

Calmodulin binds to the N-terminal domain of the cardiac sodium channel Nav1.5.

Cardiac channelopathies: Genetic and molecular mechanisms ⬇️

Complex genetic background in a large family with Brugada syndrome

Different Phenotypes of Sarcomeric MyBPC3-Cardiomyopathy in the Same Family: Hypertrophic, Left Ventricular Noncompaction and Restrictive Phenotypes (in Association with Sarcoidosis)

Laminopathies in Russian families.

Left ventricular noncompaction: A clinical and morphological study

Myocardial Biopsy In "Idiopathic» Atrial Fibrillation And Other Arrhythmias: Nosological Diagnosis, Clinical And Morphological Parallels, And Treatment.

New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy

Prevalence of Significant Genetic Variants in Congenital Long QT Syndrome is Largely Underestimated ⬇️

Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics

The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.

The role of mutations in the SCN5A gene in cardiomyopathies.

The use of noninvasive ECG imaging for examination of a patient with Brugada syndrome.

[Eosinophilic granuloma of the parietal bone of an adult patient with BRAF mutation].