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Page 1
Multiple Chromoanasynthesis in a Rare Case of Sporadic Renal Leiomyosarcoma: A Case Report.
Front Oncol. 2020 Aug 19;10:1653. doi: 10.3389/fonc.2020.01653. eCollection 2020.
Front Oncol. 2020.
PMID: 32974204
Free PMC article.
Genetic screening of Russian Usher syndrome patients toward selection for gene therapy.
Ivanova ME, Trubilin VN, Atarshchikov DS, Demchinsky AM, Strelnikov VV, Tanas AS, Orlova OM, Machalov AS, Overchenko KV, Markova TV, Golenkova DM, Anoshkin KI, Volodin IV, Zaletaev DV, Pulin AA, Nadelyaeva II, Kalinkin AI, Barh D.
Ivanova ME, et al. Among authors: anoshkin ki.
Ophthalmic Genet. 2018 Dec;39(6):706-713. doi: 10.1080/13816810.2018.1532527. Epub 2018 Oct 25.
Ophthalmic Genet. 2018.
PMID: 30358468
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[Phenotype-genotype correlations in patients with inherited retinal diseases with p.G1961E mutation in the ABCA4 gene].
Sheremet NL, Grushke IG, Zhorzholadze NV, Ronzina IA, Mikaelyan AA, Kadyshev VV, Tanas AS, Anoshkin KI, Strelnikov VV.
Sheremet NL, et al. Among authors: anoshkin ki.
Vestn Oftalmol. 2019;135(4):10-18. doi: 10.17116/oftalma201913504110.
Vestn Oftalmol. 2019.
PMID: 31573552
Russian.
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Comprehensive Molecular Genetic Diagnostics of Birt-Hogg-Dube Syndrome in a Russian Patient with Renal Cancer and Lung Cysts: A Case Report.
Mikhaylenko DS, Matveev VB, Filippova MG, Anoshkin KI, Kozlov NA, Khachaturyan AV, Semyanikhina AV, Nifatov SD, Tanas AS, Nemtsova MV, Zaletayev DV.
Mikhaylenko DS, et al. Among authors: anoshkin ki.
Case Rep Oncol. 2021 Jun 18;14(2):963-971. doi: 10.1159/000516763. eCollection 2021 May-Aug.
Case Rep Oncol. 2021.
PMID: 34703430
Free PMC article.
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New Regions With Molecular Alterations in a Rare Case of Insulinomatosis: Case Report With Literature Review.
Anoshkin K, Vasilyev I, Karandasheva K, Shugay M, Kudryavtseva V, Egorov A, Gurevich L, Mironova A, Serikov A, Kutsev S, Strelnikov V.
Anoshkin K, et al.
Front Endocrinol (Lausanne). 2021 Oct 19;12:760154. doi: 10.3389/fendo.2021.760154. eCollection 2021.
Front Endocrinol (Lausanne). 2021.
PMID: 34737724
Free PMC article.
Review.
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Pediatric chordoma associated with tuberous sclerosis complex: A rare case report with a thorough analysis of potential therapeutic molecular targets.
Anoshkin K, Zosen D, Karandasheva K, Untesco M, Volodin I, Alekseeva E, Parfenenkova A, Snegova E, Kim A, Dorofeeva M, Kutsev S, Strelnikov V.
Anoshkin K, et al.
Heliyon. 2022 Aug 19;8(8):e10291. doi: 10.1016/j.heliyon.2022.e10291. eCollection 2022 Aug.
Heliyon. 2022.
PMID: 36051260
Free PMC article.
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Specific Features of Focal Cortical Dysplasia in Tuberous Sclerosis Complex.
Bychkova E, Dorofeeva M, Levov A, Kislyakov A, Karandasheva K, Strelnikov V, Anoshkin K.
Bychkova E, et al.
Curr Issues Mol Biol. 2023 May 3;45(5):3977-3996. doi: 10.3390/cimb45050254.
Curr Issues Mol Biol. 2023.
PMID: 37232723
Free PMC article.
Review.
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[Prognostic value of TERT mutation in adults with primary glioblastomas. Preliminary results].
Zolotova SV, Anoshkin KI, Absalyamova OV, Makashova ES, Belyashova AS, Telysheva EN, Golanov AV.
Zolotova SV, et al. Among authors: anoshkin ki.
Zh Vopr Neirokhir Im N N Burdenko. 2022;86(3):33-40. doi: 10.17116/neiro20228603133.
Zh Vopr Neirokhir Im N N Burdenko. 2022.
PMID: 35758076
Russian.
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