Zobrazeno 1 - 10
of 10
pro vyhledávání: '"O P Khlebnikova"'
Autor:
Yu V Rumyantseva, A I Karachunsky, O V Aleinikova, L G Fechina, A V Shamardina, D V Litvinov, N I Ponomareva, E G Boichenko, S A Dudkin, O V Streneva, K L Kondratchik, E G Mansurova, L M Minkina, E S Lapotentova, E V Inyushkina, N B Yudina, G P Pavlova, E V Zhukovskaya, O P Khlebnikova, S N Lagoiko, E V Basharova, R E Denisov, V D Zlobina, E S Banshchikova, K S Aslanyan, E V Kondakova, E V Tselousova, N V Myakova, T V Turobova, O V Ryskal, N F Chipsanova, S R Varfolomeyeva, A G Rumyantsev
Publikováno v:
Терапевтический архив, Vol 82, Iss 7, Pp 11-19 (2010)
Aim. To evaluate the efficiency of the original ALL-MB-2002 protocol within the multicenter study of treatment of acute lymphoblastic leukemia (ALL) in children. Subjects and methods. A total of 1873 primary patients with ALL aged 1 to 18 years, of w
Externí odkaz:
https://doaj.org/article/cfbc2ada713446ef93c73a86b57fd3bc
Autor:
M. Yu. Goroshkova, Yu. V. Rumyantseva, O. V. Aleinikova, S. A. Dudkin, L. G. Fechina, A. V. Shamardina, O. V. Streneva, K. L. Kondratchik, L. M. Minkina, E. S. Lapotentova, E. V. Inyushkina, O. B. Kozlova, E. V. Zhukovskaya, O. P. Khlebnikova, E. V. Basharova, V. N. Timofeeva, G. P. Pavlova, V. D. Zlobina, O. A. Utrobina, E. S. Banshchikova, K. S. Aslanyan, E. V. Kondakova, E. V. Tselousova, N. V. Myakova, T. V. Turobova, O. V. Ryskal, O. Yu. Fuks, V. V. Lebedev, N. F. Chipsanova, S. R. Varfolomeeva, A. I. Karachunsky
Publikováno v:
Онкогематология, Vol 0, Iss 3, Pp 25-33 (2022)
The paper presents the results of a multicenter randomized study of two-dose COLI-ASP regimens in therapy of consolidation of standard risk-group (SRG) children and adolescents with acute lymphoblastic leukemia (ALL) treated by the ALL-MB-2002 protoc
Externí odkaz:
https://doaj.org/article/273ffc5c215a492e9db3020d5e11e678
Autor:
E. V. Samochatova, D. D. Baidildina, M. A. Maschan, N. N. Savva, O. P. Khlebnikova, A. V. Shamardina, Yu. E. Mareiko, G. A. Tsaur, T. O. Riger, M. M. Shneider, Yu. V. Rumyantseva, T. V. Nasedkina, T. V. Savitskaya, A. A. Maschan
Publikováno v:
Онкогематология, Vol 0, Iss 3, Pp 8-17 (2022)
The use of all-trans retinoic acid (ATRA) drastically improved the results of therapy for acute promyelocytic leukeimia (APL). The high efficiency of the Russian protocol APL-93—98 applied to 62 children and adolescents with APL (event-free and ove
Externí odkaz:
https://doaj.org/article/a1999c503e6849b689ddc0507d049b22
Publikováno v:
Русский журнал детской неврологии, Vol 14, Iss 1, Pp 49-53 (2019)
Gillespie syndrome is one of the rare monogenic syndromes characterized by a combination of congenital muscular hypotonia, delayed psychomotor and speech development, ataxia and hypoplasia of the iris. The cause of disease – homozygous, compound he
Externí odkaz:
https://doaj.org/article/5b3415033f114fb6abaf26405d530235
Autor:
O. V. Khlebnikova, I. V. Sharkova
Publikováno v:
Российский офтальмологический журнал, Vol 12, Iss 1, Pp 97-101 (2019)
Purpose: to present a clinical case of retinal abiotrophy in mitochondrial pathology (NARP syndrome) caused by the mutation m.8993T>G in the ATPase gene type 6 in order to improve the diagnosis of hereditary abiotrophies. Material and methods. The re
Externí odkaz:
https://doaj.org/article/de5a464a6b5d4eb1825e06660a6b7015
Autor:
A. M. Popov, Y. Yu. Verzhbitskaya, G. A. Tsaur, A. G. Solodovnikov, O. R. Arakaev, O. V. Streneva, O. P Khlebnikova, E. V. Shorikov, L. I. Saveliev, S. N. Lagoyko, Yu. V. Rumyantseva, A. I. Karachunskiy, L. G. Fechina
Publikováno v:
Онкогематология, Vol 10, Iss 4, Pp 44-55 (2015)
191 consecutive unselected children with acute lymphoblastic leukemia aged from 1 to 16 years were enrolled in the study. Bone marrow samples were obtained at the time of initial diagnostics as well as at days 15 (n = 188), 36 (n = 191), and 85 (n =
Externí odkaz:
https://doaj.org/article/0218a3540de14fb58723611f40943264
Autor:
B. E. Malyugin, S. A. Borzenok, O. V. Khlebnikova, M. F. Shurygina, P. M. Arbukhanova, A. N. Loginova, P. L. Volodin, S. A. Zubareva
Publikováno v:
Офтальмохирургия, Vol 0, Iss 2, Pp 42-46 (2016)
Purpose. Retrospective genetic counseling analysis of patients with hereditary retinal diseases.Material and methods. The study is based on an analysis of genetic counseling and molecular genetic studies of DNA samples of 82 patients: Stargardt disea
Externí odkaz:
https://doaj.org/article/13d94f8d25b049ea8b6cae590c2c221a
Autor:
B. E. Malyugin, S. A. Borzenok, O. V. Khlebnikova, M. F. Shurygina, P. M. Arbukhanova, A. N. Loginova, E. G. Polyanskaya, O. P. Antonova
Publikováno v:
Офтальмохирургия, Vol 0, Iss 1, Pp 63-67 (2016)
Purpose. To evaluate the results in genetic consulting of patients with various forms of congenital and hereditary eyes pathology.Material and methods. The study is based on an analysis of results in genetic consulting and molecular genetic investiga
Externí odkaz:
https://doaj.org/article/c4a54c87a7be4a75b51f8da5fc6849bc
Publikováno v:
Офтальмохирургия, Vol 0, Iss 3, Pp 97-101 (2015)
Starghardt macular dystrophy is one of the most common hereditary macular dystrophies. ABCR gene has a high level of polymorphism, multiple pathological mutations and difficult feature of inheritance. All these factors determine the special methods o
Externí odkaz:
https://doaj.org/article/e7b7135685a54340a9b7f07076d9dbd2
Autor:
O. V. Khlebnikova
Publikováno v:
Вестник Кемеровского государственного университета, Vol 0, Iss 4-1, Pp 201-207 (2013)
Despite the fact that the original philosophy emerged as a practical embodiment of love-pursuit of wisdom, in the framework of modern Western culture it should still be considered as a specific «literary» tradition of knowledge. In such circumstanc
Externí odkaz:
https://doaj.org/article/ed3edc5249484854a712ccbd4721a486