Search

Your search keyword '"Myasnikov, Roman"' showing total 13 results

Search Constraints

Start Over You searched for: Author "Myasnikov, Roman" Remove constraint Author: "Myasnikov, Roman"
13 results on '"Myasnikov, Roman"'

Search Results

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

3. Genetic landscape in Russian patients with familial left ventricular noncompaction

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

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

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

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

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

9. Omecamtiv mecarbil in chronic heart failure with reduced ejection fraction, GALACTIC‐HF: baseline characteristics and comparison with contemporary clinical trials

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

11. Back Cover, Volume 40, Issue 6

12. 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

Catalog

Books, media, physical & digital resources