Zobrazeno 1 - 10
of 110
pro vyhledávání: '"A. B. Kuzmenko"'
Publikováno v:
Communications Physics, Vol 4, Iss 1, Pp 1-9 (2021)
The experimental observation of plasmon-polaritons in charge-neutral bilayer graphene sparked interest for plasmonic and superconducting devices. Here, simulations predict that plasmon-polaritons possessing either transverse magnetic or electric pola
Externí odkaz:
https://doaj.org/article/455b140a80b347b8bc7c004ffc0d09ae
Autor:
B. Michon, A. B. Kuzmenko, M. K. Tran, B. McElfresh, S. Komiya, S. Ono, S. Uchida, D. van der Marel
Publikováno v:
Physical Review Research, Vol 3, Iss 4, p 043125 (2021)
One of the most widely discussed features of the cuprate high-T_{c} superconductors is the presence of a pseudogap in the normal state. Recent transport and specific heat measurements have revealed an abrupt transition at the pseudogap critical point
Externí odkaz:
https://doaj.org/article/2dab91c6c6424039ac18f2340f5df782
Autor:
I. Ardizzone, J. Teyssier, I. Crassee, A. B. Kuzmenko, D. G. Mazzone, D. J. Gawryluk, M. Medarde, D. van der Marel
Publikováno v:
Physical Review Research, Vol 3, Iss 3, p 033007 (2021)
The rare earth nickelates RNiO_{3} are metallic at high temperatures and insulating and magnetically ordered at low temperatures. The low temperature phase has been predicted to be type II multiferroic, i.e., ferroelectric and magnetic order are coup
Externí odkaz:
https://doaj.org/article/0e616d67062d499c91a01168f68ed5ab
Autor:
A. L. Kozlova, V. O. Bludova, V. I. Burlakov, E. V. Raykina, T. V. Varlamova, М. А. Kurnikova, А. N. Remizov, G. V. Tereshchenko, А. А. Moiseeva, S. А. Dibirova, А. L. Khoreva, А. А. Roppelt, Yu. А. Rodina, N. B. Kuzmenko, А. А. Mukhina, Е. I. Каlashnikova, L. N. Igisheva, N. V. Martynova, О. V. Zhogova, S. B. Zimin, О. V. Barabanova, Yu. V. Kotova, G. А. Novichkova, А. Yu. Shcherbina
Publikováno v:
Научно-практическая ревматология, Vol 59, Iss 3, Pp 326-334 (2021)
The aim of this study was to analyze the clinical, laboratory and molecular genetic data of 26 patients (15 boys, 11 girls) diagnosed with mevalonate kinase deficiency syndrome (MKD).Subjects and methods. The age of MKD manifestation ranged from 0 to
Externí odkaz:
https://doaj.org/article/f66c1aefc43645eeae9a70d9f988db5e
Autor:
M. E. Leontyeva, D. V. Bogdanova, A. A. Moiseeva, V. I. Burlakov, Z. A. Nesterenko, A. Y. Merkushov, N. Y. Kan, A. L. Khoreva, Y. A. Rodina, O. A. Shvets, E. A. Deordieva, N. B. Kuzmenko, A. A. Mukhina, I. V. Mersiyanova, E. V. Raikina, A. L. Kozlova
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:163-168
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e3d66b1536f404ebf365e4b0cb7f85c
https://doi.org/10.24287/1726-1708-2022-21-4-163-168
https://doi.org/10.24287/1726-1708-2022-21-4-163-168
Autor:
Anna A. Mukhina, Natalya B. Kuzmenko, Yulia A. Rodina, Irina V. Kondratenko, Andrei A. Bologov, Tatiana V. Latysheva, Andrei P. Prodeus, Alexander N. Pampura, Dmitrii N. Balashov, Natalya I. Ilyina, Elena A. Latysheva, Ekaterina A. Deordieva, Oksana A. Shvets, Elena V. Deripapa, Irina N. Abramova, Olga E. Pashenko, Svetlana S. Vahlyarskaya, Natalya V. Zinovyeva, Sergei B. Zimin, Elena V. Skorobogatova, Elena B. Machneva, Daria S. Fomina, Maria G. Ipatova, Ludmila Yu. Barycheva, Ludmila S. Khachirova, Irina A. Tuzankina, Michail A. Bolkov, Natalya V. Shakhova, Elena M. Kamaltynova, Farida I. Sibgatullina, Marina N. Guseva, Raisa N. Kuznetsova, Anzhelika M. Milichkina, Areg A. Totolian, Natalia M. Kalinina, Evgenia A. Goltsman, Ekatherina I. Sulima, Anastasia Yu. Kutlyanceva, Anna A. Moiseeva, Anna L. Khoreva, Zoya Nesterenko, Elena V. Tymofeeva, A. Ermakova, Dilyara D. Proligina, Linara R. Kalmetieva, Gulshat A. Davletbaieva, Irina A. Mirsayapova, Olga A. Richkova, Ksenia P. Kuzmicheva, Maria A. Grakhova, Natalya B. Yudina, Ekaterina A. Orlova, Olga S. Selezneva, Svetlana G. Piskunova, Tatiana V. Samofalova, Tatiana V. Bukina, Anna D. Pechkurova, N. Migacheva, A. Zhestkov, Elena V. Barmina, Natalya A. Parfenova, Svetlana N. Isakova, Elena V. Averina, Irina V. Sazonova, Svetlana Yu. Starikova, Tatiana V. Shilova, Tatiana V. Asekretova, Roman N. Suprun, Elena I. Kleshchenko, Vladimir V. Lebedev, Elena V. Demikhova, Valerii G. Demikhov, Veronica A. Kalinkina, Alla V. Gorenkova, Svetlana N. Duryagina, Tatiana B. Pavlova, Vera M. Shinkareva, Irina V. Smoleva, Tatiana P. Aleksandrova, Zema V. Bambaeva, Marina A. Philippova, Elena M. Gracheva, Galina I. Tcyvkina, Alexey V. Efremenkov, D. Mashkovskaya, Irina V. Yarovaya, Valentina A. Alekseenko, Ivan V. Fisyun, Galina V. Molokova, Ekatherina V. Troitskya, Ludmila I. Piatkina, Elena V. Vlasova, O. Ukhanova, Ekaterina G. Chernishova, M. Vasilieva, Olga M. Laba, E. Volodina, Ekaterina V. Safonova, Kirill A. Voronin, Maria V. Gurkina, Alexander G. Rumyantsev, Galina A. Novichkova, Anna Yu. Shcherbina
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Introduction: Primary immunodeficiencies (PID) are a group of rare genetic disorders with a multitude of clinical symptoms. Characterization of epidemiological and clinical data via national registries has proven to be a valuable tool of studying the
Externí odkaz:
https://doaj.org/article/6acca441337f4d1798744e22d3851bfe
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
Autor:
A. L. Kozlova, M. E. Leontieva, P. T. Velieva, M. P. Kalinina, E. A. Deordieva, O. A. Shvets, N. B. Kuzmenko, A. A. Mukhina, N. S. Grachev, G. A. Novichkova, A. Yu. Shcherbina
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:56-64
The aim of this study was to analyze the clinical and laboratory data of 101 patients (61 boys, 40 girls) diagnosed with PFAPA syndrome. The age of onset of PFAPA syndrome ranged from 8 to 36 months (the median age of onset was 18 months). The study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9194664bf218a6efbf5d65d277114c7f
https://doi.org/10.24287/1726-1708-2022-21-3-56-64
https://doi.org/10.24287/1726-1708-2022-21-3-56-64
Autor:
E. A. Viktorova, E. A. Salnikova, L. I. Papusha, V. V. Shchukin, A. V. Nechesnyuk, V. V. Gornostaev, N. B. Kuzmenko
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:136-142
Hereditary angioedema (HAE) is a disease characterized by edema of various localizations. Though classified as primary immunodeficiencz the disease lacks manifestations characteristic for primary/secondary immunodeficiencies. Medulloblastoma is one o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d9a479e96204dff08985983ea4e9971
https://doi.org/10.24287/1726-1708-2022-21-1-136-142
https://doi.org/10.24287/1726-1708-2022-21-1-136-142
Autor:
A. L. Kozlova, V. I. Burlakov, Z. A. Nesterenko, V. O. Bludova, E. V. Raykina, T. V. Varlamova, М. А. Kurnikova, A. А. Moiseeva, S. А. Dibirova, N. Yu. Kan, А. L. Horeva, А. А. Roppelt, D. V. Yukhacheva, E. V. Deripapa, Yu. А. Rodina, O. A. Shvets, E. A. Deordieva, N. B. Kuzmenko, А. А. Mukhina, G. А. Novichkova, A. Yu. Shcherbina
Publikováno v:
Pediatric Hematology/Oncology and Immunopathology. 21:88-92
The aim of this study was to analyze the clinical, laboratory and molecular genetic data of 20 patients (9 boys, 11 girls) diagnosed with cryopyrin-associated periodic syndrome (CAPS) with an assessment of the efficacy and safety of therapy in 6 pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::548d8bcc97cdb18347fe3838b114cf06
https://doi.org/10.24287/1726-1708-2022-21-1-88-92
https://doi.org/10.24287/1726-1708-2022-21-1-88-92