Roman P. Myasnikov

Moscow, MOW 101990, Russian Federation

Last Updated: 09/26/2026

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Found 12 publications

A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.

A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.

Journal: International journal of molecular sciences
Published: June 21, 2024

Genetic landscape in Russian patients with familial left ventricular noncompaction.

Genetic landscape in Russian patients with familial left ventricular noncompaction.

Journal: Frontiers in cardiovascular medicine
Published: April 14, 2023

Clinical features of pediatric Danon disease and the importance of early diagnosis.

Clinical features of pediatric Danon disease and the importance of early diagnosis.

Journal: International journal of cardiology
Published: February 15, 2023

A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.

A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.

Journal: Genes
Published: July 28, 2022

A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.

A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.

Journal: Genes
Published: December 15, 2021

The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report.

The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report.

Journal: International journal of molecular sciences
Published: May 17, 2021

Familial left ventricular noncompaction: phenotypes and clinical course. Results of the multicenter registry

Familial left ventricular noncompaction: phenotypes and clinical course. Results of the multicenter registry

Journal: Terapevticheskii arkhiv
Published: April 15, 2021

Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.

Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.

Journal: International journal of molecular sciences
Published: March 05, 2021

The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.

The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.

Journal: Genes
Published: December 14, 2020

Telemonitoring in patients with chronic heart failure

Telemonitoring in patients with chronic heart failure

Journal: Kardiologiia
Published: March 26, 2019

Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defect.

Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defect.

Journal: Human mutation
Published: October 04, 2018

Diagnostic Value of Biochemical Markers in Patients With Chronic Heart Failure With Reduced, Borderline and Preserved Left Ventricular Ejection Fraction

Diagnostic Value of Biochemical Markers in Patients With Chronic Heart Failure With Reduced, Borderline and Preserved Left Ventricular Ejection Fraction

Journal: Kardiologiia
Published: August 02, 2017
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Last Updated: 09/26/2026