Zobrazeno 1 - 10
of 14
pro vyhledávání: '"V. V. Salomashkina"'
Autor:
V I ERSHOV, I Yu GADAEV, D A BUDANOVA, F G PERINA, V L SURIN, V V SALOMASHKINA, O S PSHENICHNIKOVA, N I ZOZULYA
Publikováno v:
Терапевтический архив, Vol 90, Iss 7, Pp 118-122 (2018)
The article provides review of possible mechanisms of inhibitor coagulopathies, in particular of acquired hemophilia A. This pathology is an extremely rare disease occurring in 1-2 cases in 1 million per year. In the present study we provide data for
Externí odkaz:
https://doaj.org/article/dceae008b84d4660b41649f0670a8b2a
Autor:
D. M. Chernetskaya, V. L. Surin, V. V. Salomashkina, O. S. Pshenichnikova, E. V. Yakovleva, N. I. Zozulya, A. B. Sudarikov, E. A. Likhacheva, E. S. Shabanova, F. G. Perina
Publikováno v:
Russian journal of hematology and transfusiology. 67:172-180
Introduction. Von Willebrand disease (vWD) is caused by von Willebrand factor (vWF) dysfunction resulting from pathogenic variants in the vWF gene coding the vWF protein. vWD type 2N is of particular interest, as it is characterized by almost normal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c27bd1e7b373771ebdba47504aaf845
https://doi.org/10.35754/0234-5730-2022-67-2-172-180
https://doi.org/10.35754/0234-5730-2022-67-2-172-180
Autor:
E. V. Yakovleva, V. V. Salomashkina, V. L. Surin, D. S. Selivanova, P. S. Lavrova, L. A. Gorgidze, N. P. Soboleva, N. I. Zozulya
Publikováno v:
Russian journal of hematology and transfusiology. 67:193-201
Introduction. In most cases, in patients with hereditary fibrinogen deficiency, clinical manifestations are represented by bleeding of varying intensity and localization. However, the clinical picture of hereditary fibrinogen deficiency can also be r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55890c08e404e046ae7c7e543eec5924
https://doi.org/10.35754/0234-5730-2022-67-2-193-201
https://doi.org/10.35754/0234-5730-2022-67-2-193-201
Autor:
L L Golovkina, A G Stremoukhova, T D Pushkina, R S Kalandarov, G V Atroshchenko, M N Vasilyeva, V L Surin, V V Salomashkina, O S Pshenichnikova, G Yu Miterev, E N Parovichnikova, V G Savchenko
Publikováno v:
Терапевтический архив, Vol 88, Iss 7, Pp 78-83 (2016)
Aim. To estimate the spread of weak D antigen types of the Rhesus system in the citizens of the Russian Federation and a possibility of serologically identifying these types. Subjects and methods. The red blood cells and DNA of people with weakened e
Externí odkaz:
https://doaj.org/article/515df8a3ad8b41e295531198770563ef
Autor:
I. Yu. Gadaev, O. S. Pshenichnikova, V. V. Salomashkina, F. G. Perina, V. L. Surin, Nadezhda Zozulya, V. I. Ershov, D. A. Budanova
Publikováno v:
Терапевтический архив, Vol 90, Iss 7, Pp 118-122 (2018)
The article provides review of possible mechanisms of inhibitor coagulopathies, in particular of acquired hemophilia A. This pathology is an extremely rare disease occurring in 1-2 cases in 1 million per year. In the present study we provide data for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf1e03a3bcd052606d7ab43462b68041
https://doi.org/10.26442/terarkh2018907118-122
https://doi.org/10.26442/terarkh2018907118-122
Autor:
O. S. Pshenichnikova, D. A. Budanova, V. L. Surin, I. Yu. Gadaev, F. G. Perina, N. I. Konyashina, V. V. Salomashkina, N. I. Zozulya, O. N. Bobrova, V. I. Ershov
Publikováno v:
Russian Journal of Genetics. 54:712-716
Hemophilia A is a recessive X-linked hereditary disease, so its manifestation in women is extremely rare and can be a result of an asymmetric X-chromosome inactivation or, even more rarely, of a presence of mutations in both FVIII gene alleles. We co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2585498445e25e24cdd5c290596f81fd
https://doi.org/10.1134/s102279541806011x
https://doi.org/10.1134/s102279541806011x
Publikováno v:
Russian Journal of Genetics. 53:108-117
We perform an analysis of the diversity of the control region fragment (570 bp) and ten nuclear microsatellite loci for 36 specimens of the brown bear (Ursus arctos) from several regions of the Caucasus. Four mitochondrial haplogroups that significan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2385896a26f0a6dba98fafe357a690b7
https://doi.org/10.1134/s1022795416120103
https://doi.org/10.1134/s1022795416120103
Autor:
A. V. Polyakov, O.K. Togochakova, T. B. Milovidova, M.S. Petuhova, V.L. Surin, V. V. Salomashkina, O. A. Shchagina, E.G. Matushchenko, T. S. Beskorovainaya, E.K. Ginter, O.S. Pshenichnikova
Publikováno v:
Molekulyarnaya Meditsina (Molecular medicine). 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10f10f1111c6dac0c1268fa79564863a
https://doi.org/10.29296/24999490-2019-01-07
https://doi.org/10.29296/24999490-2019-01-07
Autor:
E Yu Demidova, V. V. Salomashkina, E. A. Likhacheva, O. S. Pshenichnikova, Yu. A. Luchinina, V. L. Surin, D. S. Selivanova
Publikováno v:
Scopus-Elsevier
Hemophilia B is a hereditary X-linked coagulation disorder. This pathology is caused by various defects in the factor IX gene, which is, being about 34 kb long and consisting of eight exons, localized in the Xq27 locus of the X-chromosome long arm. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d10173da66b7affa1ded285d4a11e050
https://doi.org/10.1134/s1022795416040116
https://doi.org/10.1134/s1022795416040116
Autor:
V L, Surin, E Yu, Demidova, D S, Selivanova, Yu A, Luchinina, V V, Salomashkina, O S, Pshenichnikova, E A, Likhacheva
Publikováno v:
Genetika. 52(4)
Hemophilia B is a hereditary X-linked coagulation disorder. This pathology is caused by various defects in the factor IX gene, which is, being about 34 kb long and consisting of eight exons, localized in the Xq27 locus of the. X-chromosome long arm.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da7e86a61c4a36fd4dcef6109eeaf9ad
https://pubmed.ncbi.nlm.nih.gov/27529981
https://pubmed.ncbi.nlm.nih.gov/27529981