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

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GENETIC ASPECTS OF MYOCARDIAL INFARCTION: PROBLEMS AND PERSPECTIVES by 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) by 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 by 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 by 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 by 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 by 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 by V. A. Shulman, S. E. Golovenkin, V. V. Rodionov, G. V. Matyushin, P. A. Shesternya

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SUBACUTE MYOCARDITIS: MYTHS AND REALITY by 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 by 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 by 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 by 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 by 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 by 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 by 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? by 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 by 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 by 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 by 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 by 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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