ADDRESS TO THE READERS حسب V. A. Shul'man

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GENETIC ASPECTS OF MYOCARDIAL INFARCTION: PROBLEMS AND PERSPECTIVES حسب P. A. Shesternya, V. A. Shulman, S. Yu. Nikulina

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CARDIAC RUPTURE IN MYOCARDIAL INFARCTION: INCIDENCE AND PREDISPOSING FACTORS (15 YEAR FOLLOW-UP) حسب V. A. Shulman, S. E. Golovenkin, V. V. Radionov, T. M. Parfenova, G. V. Matyushin

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THE ROLE OF ROS1 GENE IN DEVELOPMENT OF STROKE حسب D. A. Nikulin, D. A. Nikulina, A. A. Chernova, V. A. Shulman, S. S. Tretyakova

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FORECASTING OF CCD IN FAMILIES BY MEANS OF A METHOD OF LOGISTIC REGRESSION IN KRASNOYARSK حسب S. Yu. Nikulina, A. A. Chernova, V. A. Shulman, T. D. Vereshchagina, V. N. Chernov

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Role of SNP markers on chromosome 10 in the pathogenesis of atrial fibrillation حسب S. Yu. Nikulina, K. Yu. Shishkova, V. A. Shulman, A. A. Chernova, V. N. Maximov

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PROGNOSTIC VALUE OF PATHOLOGIC Q-WAVE AND TIME OF ITS APPEARANCE IN PATIENTS WITH MYOCARDIAL INFARCTION: COMPARISON STUDY حسب V. A. Shulman, S. E. Golovenkin, V. N. Simulin, V. V. Radionov, G. V. Matyushin

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Comparing effectiveness of tissue and plasma plasminogen activator thrombolysis in patients with various severity of acute myocardial infarction حسب V. A. Shulman, S. E. Golovenkin, V. V. Rodionov, G. V. Matyushin, P. A. Shesternya

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SUBACUTE MYOCARDITIS: MYTHS AND REALITY حسب P. A. Shesternya, V. A. Shulman, K. V. Zlodeev, E. A. Suglobova, D. V. Yurin

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PREDICTIVE ROLE OF CONNEXIN 40 IN THE PATHOGENESIS OF HEREDITARY SICK SINUS SYNDROME حسب S. Yu. Nikulina, A. A. Chernova, V. A. Shulman, T. S. Kukushkina, M. I. Voevoda, V. N. Maksimov

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THE POLYMORPHISM OF Α2B-ADRENERGIC RECEPTOR GENE — A NEW GENETIC MARKER OF THE HEREDITARY SICK SINUS SYNDROME حسب S. Iu. Nikulina, V. A. Shulman, A. A. Chernova, D. A. Nikulin, M. I. Voevoda, V. N. Maksimov

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GIANT CELL MYOCARDITIS IN HIV INFECTION: A FATAL TANDEM حسب S. Yu. Nikulina, P. A. Shesternya, A. K. Kirichenko, A. A. Chernova, D. A. Brusentsov, V. A. Shulman

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PROSPECTS FOR THE USE OF GENOTYPING FOR CHROMOSOME 9p21.3 POLYMORPHISMS FOR MYOCARDIAL INFARCTION RISK STRATIFICATION IN YOUNG PEOPLE حسب P. A. Shesternya, S. Yu. Nikulina, V. A. Shulman, E. A. Martynova, A. I. Demkina, V. V. Kozlov

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FIRST RUSSIA-BASED STUDY OF POLYMORPHISM rs2200733 CHROMOSOME 4q25 ASSOCIATION WITH DEVELOPMENT OF THE LONE ATRIAL FIBRILLATION حسب V. A. Shulman, S. Yu. Nikulina, N. V. Aksyutina N, E. E. Poplavskaya, B. V. Nazarov, V. N. Maksimov

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AN INHERITANCE OF IDIOPATHIC CARDIAC CONDUCTION DISORDERS حسب S. S. Tretyakova, S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, V. N. Maksimov, M. I. Voevoda, V. N. Chernov

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CLINICAL SIGNIFICANCE OF CORONARY ARTERY DISEASE GENETIC MARKERS: REALITY OR FAR FUTURE? حسب P. A. Shesternya, S. Yu. Nikulina, V. A. Shulman, A. S. Sergeeva, A. I. Demkina, V. N. Maksimov, М. I. Voevoda

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CLINICAL-GENETIC RISKOMETER FOR THE ISCHEMIC STROKE RISK ASSESSMENT IN ATRIAL FIBRILLATION حسب N. V. Aksyutina, V. A. Shulman, S. Yu. Nikulina, B. V. Nazarov, V. N. Maksimov, E. V. Plita, M. Yu. Kotlovsky, T. D. Vereshchagina

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PREDICTIVE ROLE OF CHROMOSOME 9P21.3 POLYMORPHISMS AND THEIR ASSOCIATION WITH FAMILY HISTORY OF CORONARY HEART DISEASE IN PATIENTS WITH MYOCARDIAL INFARCTION حسب P. A. Shesternya, V. A. Shulman, S. Yu. Nikulina, E. A. Martynova, A. I. Demkina, P. S. Orlov, V. N. Maksimov, M. I. Voevoda

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Association of rs556621 Polymorphism with Development of Stroke in Patients with Cardiovascular Pathology حسب S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, S. V. Prokopenko, D. A. Nikulin, I. M. Platunova, S. S. Tretyakova, V. N. Maksimov, A. A. Gurazheva

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Role of Single Nucleotide Polymorphism of СУР17А Gene in the Development of Stroke حسب S. Yu. Nikulina, V. A. Shulman, A. A. Chernova, D. A. Nikulin, A. A. Semenchukov, O. V. Marilovceva, S. S. Tret'jakova, I. I. Lebedeva, V. N. Maksimov

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