Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2020 | 1 |
2022 | 2 |
2023 | 3 |
2024 | 0 |
Search Results
7 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Factor XII deficiency: a clinical and molecular genetic study.
Int J Hematol. 2023 May;117(5):678-683. doi: 10.1007/s12185-023-03535-9. Epub 2023 Jan 10.
Int J Hematol. 2023.
PMID: 36627437
Spectrum of Causative Mutations in Patients with Hemophilia A in Russia.
Pshenichnikova O, Salomashkina V, Poznyakova J, Selivanova D, Chernetskaya D, Yakovleva E, Dimitrieva O, Likhacheva E, Perina F, Zozulya N, Surin V.
Pshenichnikova O, et al.
Genes (Basel). 2023 Jan 19;14(2):260. doi: 10.3390/genes14020260.
Genes (Basel). 2023.
PMID: 36833187
Free PMC article.
Item in Clipboard
Molecular Genetic Analysis of Russian Patients with Coagulation Factor FVII Deficiency.
Pshenichnikova O, Selivanova D, Shchemeleva E, Abramova T, Zozulya N, Surin V.
Pshenichnikova O, et al.
Genes (Basel). 2023 Sep 6;14(9):1767. doi: 10.3390/genes14091767.
Genes (Basel). 2023.
PMID: 37761907
Free PMC article.
Item in Clipboard
A founder effect in hemophilia A patients from Russian Ural region with a new p.(His634Arg) variant in F8 gene.
Salomashkina VV, Pshenichnikova OS, Perina FG, Surin VL.
Salomashkina VV, et al. Among authors: pshenichnikova os.
Blood Coagul Fibrinolysis. 2022 Mar 1;33(2):124-129. doi: 10.1097/MBC.0000000000001073.
Blood Coagul Fibrinolysis. 2022.
PMID: 34393174
Item in Clipboard
Molecular genetic study of acute intermittent porphyria in Russia: HMBS gene mutation spectrum and problem of penetrance.
Goncharova M, Pshenichnikova O, Luchinina Y, Pustovoit Y, Karpova I, Surin V.
Goncharova M, et al. Among authors: pshenichnikova o.
Clin Genet. 2019 Jul;96(1):91-97. doi: 10.1111/cge.13558. Epub 2019 May 14.
Clin Genet. 2019.
PMID: 31044425
Item in Clipboard
New missense mutation p.Trp387Ser affecting the functionally important TrpXXTrp motif in the TSR1 repeat of ADAMTS13 metalloproteinase: Case report.
Poznyakova J, Pshenichnikova O, Surin V, Klebanova E, Galstyan G.
Poznyakova J, et al. Among authors: pshenichnikova o.
Clin Exp Pharmacol Physiol. 2022 Nov;49(11):1150-1155. doi: 10.1111/1440-1681.13697. Epub 2022 Jul 22.
Clin Exp Pharmacol Physiol. 2022.
PMID: 35762256
Item in Clipboard
Immunophenotypic characteristics of multipotent mesenchymal stromal cells that affect the efficacy of their use in the prevention of acute graft vs host disease.
Petinati N, Kapranov N, Davydova Y, Bigildeev A, Pshenichnikova O, Karpenko D, Drize N, Kuzmina L, Parovichnikova E, Savchenko V.
Petinati N, et al. Among authors: pshenichnikova o.
World J Stem Cells. 2020 Nov 26;12(11):1377-1395. doi: 10.4252/wjsc.v12.i11.1377.
World J Stem Cells. 2020.
PMID: 33312405
Free PMC article.
Item in Clipboard
Cite
Cite