Genetic landscape in Russian patients with familial left ventricular noncompaction von Meshkov, Alexey N, Myasnikov, Roman P, Kiseleva, Anna V, Kulikova, Olga V, Sotnikova, Evgeniia A, Kudryavtseva, Maria M, Zharikova, Anastasia A, Koretskiy, Sergey N, Mershina, Elena A, Ramensky, Vasily E, Zaicenoka, Marija, Vyatkin, Yuri V, Kharlap, Maria S, Nikityuk, Tatiana G, Sinitsyn, Valentin E, Divashuk, Mikhail G, Kutsenko, Vladimir A, Basargina, Elena N, Barskiy, Vladimir I, Sdvigova, Nataliya A, Skirko, Olga P, Efimova, Irina A, Pokrovskaya, Maria S, Drapkina, Oxana M

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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 von Marakhonov, Andrey V., Brodehl, Andreas, Myasnikov, Roman P., Sparber, Peter A., Kiseleva, Anna V., Kulikova, Olga V., Meshkov, Alexey N., Zharikova, Anastasia A., Koretsky, Serguey N., Kharlap, Maria S., Stanasiuk, Caroline, Mershina, Elena A., Sinitsyn, Valentin E., Shevchenko, Alexey O., Mozheyko, Natalia P., Drapkina, Oksana M., Boytsov, Sergey A., Milting, Hendrik, Skoblov, Mikhail Yu

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A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy von Myasnikov, Roman P, Kulikova, Olga V, Meshkov, Alexey N, Bukaeva, Anna A, Kiseleva, Anna V, Ershova, Alexandra I, Petukhova, Anna V, Divashuk, Mikhail G, Zotova, Evgenia D, Sotnikova, Evgeniia A, Abisheva, Alexandra A, Muraveva, Alisa V, Koretskiy, Sergey N, Popov, Sergey V, Utkina, Marina V, Snigir, Ekaterina A, Mitrofanov, Sergey I, Konureeva, Ksenia D, Mershina, Elena A, Sinitsyn, Valentin E, Yudin, Sergey M, Drapkina, Oxana M

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Familial left ventricular noncompaction: phenotypes and clinical course. Results of the multicenter registry von Kulikova, Olga, Myasnikov, Roman P., Mershina, Elena A., Pilus, Polina S., Koretskiy, Sergei N., Meshkov, Aleksei N., Kiseleva, Anna, Kharlap, Mariia S., Sinitsyn, Valentin E., Sdvigova, Nataliia A., Gandaeva, Leila A., Barskiy, Vladimir, Derevnina, Yuliia, Zharova, Olga P., Basargina, Elena N., Boytsov, Sergey A., Drapkina, Oksana M.

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Body composition and functional activity in men with heart failure von Skripnikova, I. A., Yaralieva, E. K., Myasnikov, R. P., Kulikova, O. V., Novikov, V. E., Kosmatova, O. V., Vygodin, V. A., Drapkina, O. M.

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Back Cover, Volume 40, Issue 6 von Marakhonov, Andrey V., Brodehl, Andreas, Myasnikov, Roman P., Sparber, Peter A., Kiseleva, Anna V., Kulikova, Olga V., Meshkov, Alexey N., Zharikova, Anastasia A., Koretsky, Serguey N., Kharlap, Maria S., Stanasiuk, Caroline, Mershina, Elena A., Sinitsyn, Valentin E., Shevchenko, Alexey O., Mozheyko, Natalia P., Drapkina, Oksana M., Boytsov, Sergey A., Milting, Hendrik, Skoblov, Mikhail Yu

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A Splice Variant of the IMYH7/I Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy von Myasnikov, Roman P, Kulikova, Olga V, Meshkov, Alexey N, Bukaeva, Anna A, Kiseleva, Anna V, Ershova, Alexandra I, Petukhova, Anna V, Divashuk, Mikhail G, Zotova, Evgenia D, Sotnikova, Evgeniia A, Abisheva, Alexandra A, Muraveva, Alisa V, Koretskiy, Sergey N, Popov, Sergey V, Utkina, Marina V, Snigir, Ekaterina A, Mitrofanov, Sergey I, Konureeva, Ksenia D, Mershina, Elena A, Sinitsyn, Valentin E, Yudin, Sergey M, Drapkina, Oxana M

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New Variant of MYH7 Gene Nucleotide Sequence in Familial Non-Compaction Cardiomyopathy with Benign Course von Myasnikov, R. P., Kulikova, O. V., Meshkov, A. N., Kiseleva, A. V., Shumarina, A. O., Koretskiy, S. N., Zharikova, A. A., Divashuk, M. G., Kharlap, M. S., Serduk, S. E., Mershina, E. A., Sinitsyn, V. E., Boytsov, S. A., Drapkina, O. M.

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Systemic ATTR-amyloidosis, a Rare Form of Internal Organ Damage von Rameev, V. V., Myasnikov, R. P., Vinogradov, P. P., Kozlovskaya, L. V., Moiseev, S. V., Fomicheva, E. I., Beregovskaya, S. A., Mershina, E. A., Kostina, S. A., Strizhakov, L. A., Rameeva, A. S., Tao, P. P., Drapkina, O. M.

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