Voinova VY - Search Results

1

40-Hz Auditory Steady-State Response (ASSR) as a Biomarker of Genetic Defects in the SHANK3 Gene: A Case Report of 15-Year-Old Girl with a Rare Partial SHANK3 Duplication.

Neklyudova AK, Portnova GV, Rebreikina AB, Voinova VY, Vorsanova SG, Iourov IY, Sysoeva OV. Neklyudova AK, et al. Among authors: voinova vy. Int J Mol Sci. 2021 Feb 14;22(4):1898. doi: 10.3390/ijms22041898. Int J Mol Sci. 2021. PMID: 33673024 Free PMC article.

2

Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: a search for familial genetic markers for autistic disorders.

Vorsanova SG, Voinova VY, Yurov IY, Kurinnaya OS, Demidova IA, Yurov YB. Vorsanova SG, et al. Among authors: voinova vy. Neurosci Behav Physiol. 2010 Sep;40(7):745-56. doi: 10.1007/s11055-010-9321-5. Neurosci Behav Physiol. 2010. PMID: 20635215

3

Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease.

Iourov IY, Vorsanova SG, Voinova VY, Kurinnaia OS, Zelenova MA, Demidova IA, Yurov YB. Iourov IY, et al. Among authors: voinova vy. Mol Cytogenet. 2013 Nov 27;6(1):53. doi: 10.1186/1755-8166-6-53. Mol Cytogenet. 2013. PMID: 24283533 Free PMC article.

4

3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances.

Iourov IY, Vorsanova SG, Voinova VY, Yurov YB. Iourov IY, et al. Among authors: voinova vy. Mol Cytogenet. 2015 Oct 31;8:82. doi: 10.1186/s13039-015-0185-9. eCollection 2015. Mol Cytogenet. 2015. PMID: 26523151 Free PMC article.

5

[Clinical and genetic characteristics of the X chromosome distal long arm microduplications encompassing the MECP2 gene].

Voinova VY, Vorsanova SG, Yurov YB, Kolotiy AD, Davidova YI, Demidova IA, Novikov PV, Iourov IY. Voinova VY, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2015;115(10):10-16. doi: 10.17116/jnevro201511510110-16. Zh Nevrol Psikhiatr Im S S Korsakova. 2015. PMID: 26525614 Russian.

6

Complex Diagnostics of Non-Specific Intellectual Developmental Disorder.

Levchenko O, Dadali E, Bessonova L, Demina N, Rudenskaya G, Matyushchenko G, Markova T, Anisimova I, Semenova N, Shchagina O, Ryzhkova O, Zinchenko R, Galkina V, Voinova V, Nagieva S, Lavrov A. Levchenko O, et al. Int J Mol Sci. 2022 Jul 14;23(14):7764. doi: 10.3390/ijms23147764. Int J Mol Sci. 2022. PMID: 35887114 Free PMC article.

7

Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population.

Glotov OS, Savostyanov KV, Nagornova TS, Chernov AN, Fedyakov MA, Raspopova AN, Krasnoukhov KN, Danilov LG, Moiseeva NV, Kalinin RS, Tsai VV, Eismont YA, Voinova VY, Vitebskaya AV, Gurkina EY, Kuzenkova LM, Sosnina IB, Pushkov AA, Zhanin IS, Zakharova EY. Glotov OS, et al. Among authors: voinova vy. Int J Mol Sci. 2022 Oct 26;23(21):12976. doi: 10.3390/ijms232112976. Int J Mol Sci. 2022. PMID: 36361766 Free PMC article.

8

Clinical EEG of Rett Syndrome: Group Analysis Supplemented with Longitudinal Case Report.

Portnova G, Neklyudova A, Voinova V, Sysoeva O. Portnova G, et al. J Pers Med. 2022 Nov 29;12(12):1973. doi: 10.3390/jpm12121973. J Pers Med. 2022. PMID: 36556193 Free PMC article.

9

Abnormal spectral and scale-free properties of resting-state EEG in girls with Rett syndrome.

Sysoeva O, Maximenko V, Kuc A, Voinova V, Martynova O, Hramov A. Sysoeva O, et al. Sci Rep. 2023 Aug 9;13(1):12932. doi: 10.1038/s41598-023-39398-7. Sci Rep. 2023. PMID: 37558701 Free PMC article.

10

Effect of presentation rate on auditory processing in Rett syndrome: event-related potential study.

Kostanian D, Rebreikina A, Voinova V, Sysoeva O. Kostanian D, et al. Mol Autism. 2023 Oct 26;14(1):40. doi: 10.1186/s13229-023-00566-1. Mol Autism. 2023. PMID: 37885019 Free PMC article.

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