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Items: 1 to 20 of 57

1.

[Bilateral supraorbital keyhole approach in surgery of multiple cerebral aneurysms: a case report and literature review].

Dzhindzhikhadze RS, Dreval' ON, Lazarev VA, Kambiev RL, Polyakov AV.

Zh Vopr Neirokhir Im N N Burdenko. 2019;83(3):93-101. doi: 10.17116/neiro20198303193. Russian.

PMID:
31339502
2.

X-linked hypohidrotic ectodermal dysplasia: clinical and molecular genetic analysis of a large Russian family with a synonymous p.Ser267= (c.801A>G) splice site mutation.

Milovidova TB, Schagina OA, Freire MV, Demina NA, Filatova AY, Skoblov MY, Stepanova AA, Chuhrova AL, Polyakov AV.

J Eur Acad Dermatol Venereol. 2019 Jul 15. doi: 10.1111/jdv.15798. [Epub ahead of print] No abstract available.

PMID:
31306530
3.

A new case of infantile-onset hereditary spastic paraplegia with complicated phenotype (SPG61) in a consanguineous Russian family.

Chukhrova AL, Akimova IA, Shchagina OA, Kadnikova VA, Ryzhkova OP, Polyakov AV.

Eur J Neurol. 2019 May;26(5):e61-e62. doi: 10.1111/ene.13880. No abstract available.

PMID:
30980493
4.

Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.

Petrova NV, Kashirskaya NY, Saydaeva DK, Polyakov AV, Adyan TA, Simonova OI, Gorinova YV, Kondratyeva EI, Sherman VD, Novoselova OG, Vasilyeva TA, Marakhonov AV, Macek M Jr, Ginter EK, Zinchenko RA.

BMC Med Genet. 2019 Mar 21;20(1):44. doi: 10.1186/s12881-019-0785-z.

5.

Genotypes of 2579 patients with phenylketonuria reveal a high rate of BH4 non-responders in Russia.

Gundorova P, Stepanova AA, Kuznetsova IA, Kutsev SI, Polyakov AV.

PLoS One. 2019 Jan 22;14(1):e0211048. doi: 10.1371/journal.pone.0211048. eCollection 2019.

6.

Transpalpebral approach in skull base surgery: how I do it.

Dzhindzhikhadze RS, Dreval ON, Lazarev VA, Polyakov AV.

Acta Neurochir (Wien). 2019 Jan;161(1):133-137. doi: 10.1007/s00701-018-3724-4. Epub 2018 Nov 9.

PMID:
30413939
7.

Study of the genetic load and diversity of hereditary diseases in the Russian population of the Karachay-Cherkess Republic.

Zinchenko RA, Kadyshev VV, El'chinova GI, Marakhonov AV, Galkina VA, Dadali EL, Khlebnikova OV, Mikhailova LK, Petrova NV, Petrina NE, Vasilyeva TA, Gundorova P, Tanas AS, Strelnikov VV, Polyakov AV, Ginter EK.

Int J Mol Epidemiol Genet. 2018 Aug 20;9(4):34-42. eCollection 2018.

8.

[Endoscope-assisted keyhole approach in cerebral aneurysm surgery].

Dzhindzhikhadze RS, Dreval' ON, Lazarev VA, Polyakov AV, Kambiev RL, Davudov AM.

Zh Vopr Neirokhir Im N N Burdenko. 2018;82(4):38-44. doi: 10.17116/neiro201882438. Russian.

PMID:
30137037
9.

[The analysis of the association of the polymorphic variants of the TPMT, COMT, and ABCC3 genes with the development of hearing disorders induced by the cisplatin treatment].

Mironovich OL, Bliznetz EA, Garbaruk ES, Belogurova MB, Subora NV, Varfolomeeva SR, Kachanov DY, Shamanskaya TV, Markova TG, Polyakov AV.

Vestn Otorinolaringol. 2018;83(4):60-66. doi: 10.17116/otorino201883460. Russian.

PMID:
30113582
10.

[Epidemiology of hearing loss in children of the first year of life].

Chibisova SS, Markova TG, Alekseeva NN, Yasinskaya AA, Tsygankova ER, Bliznetz EA, Polyakov AV, Tavartkiladze GA.

Vestn Otorinolaringol. 2018;83(4):37-42. doi: 10.17116/otorino201883437. Russian.

PMID:
30113578
11.

[Twenty years of clinical studies of GJB2-linked hearing loss in Russia].

Markova TG, Bliznetz EA, Polyakov AV, Tavartkiladze GA.

Vestn Otorinolaringol. 2018;83(4):31-36. doi: 10.17116/otorino201883431. Russian.

PMID:
30113577
12.

Molecular-genetic causes for the high frequency of phenylketonuria in the population from the North Caucasus.

Gundorova P, Zinchenko RA, Kuznetsova IA, Bliznetz EA, Stepanova AA, Polyakov AV.

PLoS One. 2018 Aug 1;13(8):e0201489. doi: 10.1371/journal.pone.0201489. eCollection 2018.

13.

Molybdenum Disulfide Surface Modification of Ultrafine-Grained Titanium for Enhanced Cellular Growth and Antibacterial Effect.

Shin MH, Baek SM, Polyakov AV, Semenova IP, Valiev RZ, Hwang WB, Hahn SK, Kim HS.

Sci Rep. 2018 Jul 2;8(1):9907. doi: 10.1038/s41598-018-28367-0.

14.

[The transpalpebral keyhole approach in surgery of orbital cavernomas: a case report and literature review].

Dzhindzhikhadze RS, Dreval' ON, Lazarev VA, Polyakov AV.

Zh Vopr Neirokhir Im N N Burdenko. 2018;82(3):73-80. doi: 10.17116/neiro201882373. Review. Russian.

15.

[Neurological presentations of oculodentodigital dysplasia].

Rudenskaya GE, Dyomina NA, Bliznetz EA, Khlebnikova OV, Dadaly EL, Polyakov AV.

Zh Nevrol Psikhiatr Im S S Korsakova. 2018;118(5):85-91. doi: 10.17116/jnevro20181185185. Russian.

PMID:
29927410
16.

[Transpalpebral craniotomy in skull base surgery].

Dzhindzhikhadze RS, Dreval' ON, Lazarev VA, Polyakov AV, Kambiev RL.

Zh Vopr Neirokhir Im N N Burdenko. 2018;82(2):48-58. doi: 10.17116/oftalma201882248-58. Russian.

17.

[Results of molecular genetic testing in Russian patients with Pendred syndrome and allelic disorders].

Mironovich OL, Bliznetz EA, Markova TG, Geptner EN, Lalayants MR, Zelikovich EI, Tavartkiladze GA, Polyakov AV.

Genetika. 2017 Jan;53(1):88-99. Russian.

PMID:
29372807
18.

Chromosome Synapsis and Recombination in Male Hybrids between Two Chromosome Races of the Common Shrew (Sorex araneus L., Soricidae, Eulipotyphla).

Belonogova NM, Polyakov AV, Karamysheva TV, Torgasheva AA, Searle JB, Borodin PM.

Genes (Basel). 2017 Oct 20;8(10). pii: E282. doi: 10.3390/genes8100282.

19.

[Molecular genetic diagnosis of Stargardt disease].

Sheremet NL, Zhorzholadze NV, Ronzina IA, Grushke IG, Kurbatov SA, Chukhrova AL, Loginova AN, Shcherbakova PO, Tanas AS, Polyakov AV, Strel'nikov VV.

Vestn Oftalmol. 2017;133(4):4-11. doi: 10.17116/oftalma201713344-11. Russian.

20.

Study of male-mediated gene flow across a hybrid zone in the common shrew (Sorex araneus) using Y chromosome.

Polyakov AV, Panov VV.

Comp Cytogenet. 2017 Jun 19;11(2):421-430. doi: 10.3897/CompCytogen.v11i2.13494. eCollection 2017.

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