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European Heart Journal, ISSN 0195-668X, 08/2018, Volume 39, Issue suppl_1
Journal Article
European Heart Journal, ISSN 0195-668X, 08/2018, Volume 39, Issue suppl_1
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2013, Volume 71, Issue Suppl 3, pp. 639 - 639
Background The development of secondary (AA) amyloidosis in rheumatoid arthritis (RA) is considered to be extensively determined by genotype characteristics.... 
Journal Article
Российский кардиологический журнал, ISSN 1560-4071, 05/2019, Issue 4, pp. 35 - 47
Dilated cardiomyopathy (DCM) is a complex, etiologically heterogeneous myocardial disease, which is one of the main causes of heart failure and heart... 
RBM20 | gene mutations | genetic testing | LMNA | dilated cardiomyopathy | laminopathy
Journal Article
Российский кардиологический журнал, ISSN 1560-4071, 11/2018, Issue 10, pp. 151 - 158
Mutations in the genes encoding desmosomal proteins cause a wide range of diseases associated with abnormalities of the skin, hair and heart. In 45-50% these... 
desmoplakin | Naxos syndrome | placoglobin | keratoderma | dilated cardiomyopathy | wooly hair | Carvajal syndrome
Journal Article
Российский кардиологический журнал, ISSN 1560-4071, 11/2017, Issue 10, pp. 93 - 99
Danon disease (DD) is a rare and complex pathology, difficult for diagnostics, with multisystemic presentation, which demands for multidisciplinary clinical... 
hypertrophic cardiomyopathy | LAMP2 | Danon disease
Journal Article
Российский кардиологический журнал, ISSN 1560-4071, 11/2016, Issue 11, pp. 90 - 94
Recent decades significantly increased the spectrum of monogenic diseases associated with mutations in the gene of lamin A/C (LMNA), that codes the... 
lamin gene mutations А/С | hypergonadotropic hypogonadism | dilation cardiomyopathy
Journal Article
Российский кардиологический журнал, ISSN 1560-4071, 11/2016, Issue 11, pp. 27 - 35
Search for effective methods of risk stratification in patients with higher risk of lifethreatening ventricular tachyarrhythmias (VTA) and sudden cardiac death... 
dilation cardiomyopathy | risk stratification | sudden cardiac death | lamin A/C genes mutation | markers of electrical instability of myocardium
Journal Article
Kardiologiia, ISSN 0022-9040, 05/2016, Volume 56, Issue 5, p. 85
Dilated cardiomyopathy (DCM) caused by mutations in the lamin A/C (LMNA) gene is often associated with conduction disorders, cardiac arrhythmias and various... 
Phenotype | Dilatation | Pedigree | Humans | Lamin Type A | Mutation | Cardiomyopathy, Dilated
Journal Article
Russian Journal of Cardiology, ISSN 1560-4071, 2019, Volume 24, Issue 4, pp. 35 - 47
Dilated cardiomyopathy (DCM) is a complex, etiologically heterogeneous myocardial disease, which is one of the main causes of heart failure and heart... 
RBM20 | Genetic testing | Dilated cardiomyopathy | Gene mutations | Laminopathy | LMNA
Journal Article
Russian Journal of Genetics: Applied Research, ISSN 2079-0597, 4/2012, Volume 2, Issue 2, pp. 114 - 121
A study of the R1a1a7 (M458) haplogroup in ethnic Belarusians from six historical-ethnographic regions demonstrated that its frequency is 14.5%. A higher... 
Human Genetics | Slavs | Biomedicine | haplotype | Belarusians | haplogroup | Y chromosome
Journal Article
Russian Journal of Cardiology, ISSN 1560-4071, 2017, Volume 150, Issue 10, pp. 93 - 99
Journal Article
Russian Journal of Cardiology, ISSN 1560-4071, 2016, Volume 139, Issue 11, pp. 90 - 94
Journal Article
KARDIOLOGIYA, ISSN 0022-9040, 2018, Volume 58, pp. 33 - 46
Left ventricular non-compaction (LVNC) is characterized by hypertrabecularity (thickened non-compact layer) with deep intertrabecular recesses that are... 
MYOCARDIUM | DIAGNOSIS | TRABECULATION | CARDIAC & CARDIOVASCULAR SYSTEMS | MANIFESTATION | POSITION STATEMENT | CLASSIFICATION | Danon disease | EUROPEAN-SOCIETY | genetic heterogeneity | left ventricular non-compaction | syndrome with isolated noncompactness | NON-COMPACTION | MUTATIONS | dilated cardiomyopathy | CARDIOLOGY WORKING GROUP
Journal Article
KARDIOLOGIYA, ISSN 0022-9040, 2016, Volume 56, Issue 5, pp. 85 - 96
Dilated cardiomyopathy (DCM) caused by mutations in the lamin A/C (LMNA) gene is often associated with conduction disorders, cardiac arrhythmias and various... 
CARDIAC & CARDIOVASCULAR SYSTEMS | CONDUCTION SYSTEM | A/C MUTATIONS | classification MOGE(S) system | SUDDEN-DEATH | POSITION STATEMENT | right ventricular cardiomyopathy | EUROPEAN-SOCIETY | TASK-FORCE | arrhythmia | DISEASE | lamin gene (LMNA) | defibrillator | dilated cardiomyopathy | RIGHT-VENTRICULAR CARDIOMYOPATHY | CARDIOLOGY WORKING GROUP
Journal Article
Russian Journal of Genetics, ISSN 1022-7954, 5/2008, Volume 44, Issue 5, pp. 609 - 616
The insertion/deletion polymorphism of the angiotensin-converting enzyme gene (ACE) and the T174M polymorphism of the angiotensinogen gene (AGT) have been... 
Human Genetics | Biomedicine | Microbial Genetics and Genomics | Animal Genetics and Genomics | INSERTION/DELETION POLYMORPHISM | GENETICS & HEREDITY | T174M POLYMORPHISM | POPULATIONS | ESSENTIAL-HYPERTENSION | ASSOCIATION | LOCUS | BLOOD-PRESSURE | CONVERTING-ENZYME | I/D | Genetic aspects | Angiotensin
Journal Article
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