Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Elena V. Raykina"'
Autor:
Anton V. Luchkin, Elena A. Mikhailova, Zalina T. Fidarova, Vera V. Troitskaya, Irina V. Galtseva, Alla M. Kovrigina, Svetlana A. Glinkina, Valentina N. Dvirnyk, Elena V. Raykina, Anna V. Pavlova, Irina A. Demina, Elena N. Parovichnikova
Publikováno v:
Терапевтический архив, Vol 93, Iss 7, Pp 818-825 (2021)
Dyskeratosis congenita (DC) is a hereditary syndrome of bone marrow failure, which develops because of telomeres defects and combines with cancer predisposition. Its classical clinical features are skin pigmentation, nail dystrophy, oral leukoplakia
Externí odkaz:
https://doaj.org/article/b0b3e77cb25f4754b6351e21b015b70c
Autor:
Galina S. Ovsyannikova, Daria V. Fedorova, Ivan P. Tesakov, Alexey A. Martyanov, Anastasia A. Ignatova, Evgeniya A. Ponomarenko, Pavel A. Zharkov, Anna V. Pavlova, Elena V. Raykina, Michael A. Maschan, Mikhail A. Panteleev, Galina A. Novichkova, Anastasia N. Sveshnikova, Nataliya S. Smetanina
Publikováno v:
Haematologica, Vol 107, Iss 10 (2022)
Externí odkaz:
https://doaj.org/article/71002e0bcc1347818d3580f82e56a747
Autor:
Aleksey S. Tsukanov, Dmitriy Y. Pikunov, Vitaly P. Shubin, Aleksey A. Barinov, Vladimir N. Kashnikov, Yuri A. Shelygin, Andrey D. Kaprin, Elena V. Filonenko, Dmitriy V. Sidorov, Aleksey A. Maschan, Galina A. Novichkova, Liudmila A. Yasko, Elena V. Raykina, Aleksandr G. Rumyantsev
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
We present an extremely rare clinical case of a 38-year-old Russian patient with multiple malignant neoplasms of the uterus and colon caused by genetically confirmed two hereditary diseases: Diamond–Blackfan anemia and Lynch syndrome. Molecular gen
Externí odkaz:
https://doaj.org/article/6100ebe0e3bf4f269ece0609a55384db
Autor:
Svetlana O. Sharapova, Małgorzata Skomska-Pawliszak, Yulia A. Rodina, Beata Wolska-Kuśnierz, Nel Dabrowska-Leonik, Bozena Mikołuć, Olga E. Pashchenko, Srdjan Pasic, Tomáš Freiberger, Tomáš Milota, Renata Formánková, Anna Szaflarska, Maciej Siedlar, Tadej Avčin, Gašper Markelj, Peter Ciznar, Krzysztof Kalwak, Sylwia Kołtan, Teresa Jackowska, Katarzyna Drabko, Alenka Gagro, Małgorzata Pac, Elissaveta Naumova, Snezhina Kandilarova, Katarzyna Babol-Pokora, Dzmitry S. Varabyou, Barbara H. Barendregt, Elena V. Raykina, Tatiana V. Varlamova, Anna V. Pavlova, Hana Grombirikova, Maruša Debeljak, Irina V. Mersiyanova, Anastasiia V. Bondarenko, Liudmyla I. Chernyshova, Larysa V. Kostyuchenko, Marina N. Guseva, Jelena Rascon, Audrone Muleviciene, Egle Preiksaitiene, Christoph B. Geier, Alexander Leiss-Piller, Yasuhiro Yamazaki, Tomoki Kawai, Jolan E. Walter, Irina V. Kondratenko, Anna Šedivá, Mirjam van der Burg, Natalia B. Kuzmenko, Luigi D. Notarangelo, Ewa Bernatowska, Olga V. Aleinikova
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Background: Variants in recombination-activating genes (RAG) are common genetic causes of autosomal recessive forms of combined immunodeficiencies (CID) ranging from severe combined immunodeficiency (SCID), Omenn syndrome (OS), leaky SCID, and CID wi
Externí odkaz:
https://doaj.org/article/9b03aece41064fa7ac129d44af5c221a