Zobrazeno 1 - 10
of 52
pro vyhledávání: '"N L Gorbachevskaya"'
Publikováno v:
Neuroscience and Behavioral Physiology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b124e24a2bc3fe4269ecc1ed7c87482
https://doi.org/10.1007/s11055-023-01371-2
https://doi.org/10.1007/s11055-023-01371-2
Publikováno v:
Neuroscience and Behavioral Physiology. 47:758-766
This article presents a review of current studies addressing the early signs of autism spectrum disorder (ASD). Autism spectrum disorder is a group of developmental impairments whose main signs are qualitative impairments to communication and social
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b70c90eb0de8cb839977d08c58f5d86e
https://doi.org/10.1007/s11055-017-0464-5
https://doi.org/10.1007/s11055-017-0464-5
Autor:
E. I. Kuznetsova, N. L. Gorbachevskaya
Publikováno v:
Oncopediatrics. 4:115-122
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fca19508d53b6546b11e99e233056b01
https://doi.org/10.15690/onco.v4i2.1705
https://doi.org/10.15690/onco.v4i2.1705
Autor:
D S, Pereverzeva, N L, Gorbachevskaya
Publikováno v:
Zhurnal vysshei nervnoi deiatelnosti imeni I P Pavlova. 66(3)
The article aims to systematically review recent studies on early symptoms of autism developmental dis- orders. Autism spectrum disorders is a group of neurodevelopmental disorders that is characterized by impairment of communication and social inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6bbac16717a3963fed341c67cbc6a90
https://pubmed.ncbi.nlm.nih.gov/30695411
https://pubmed.ncbi.nlm.nih.gov/30695411
Autor:
N. N. Veiko, S M Stukalov, A B Sorokin, S. V. Kostyuk, Lev N. Porokhovnik, Elizaveta S. Ershova, N. A. Lyapunova, N. Yu. Korovina, N L Gorbachevskaya
Publikováno v:
Biomeditsinskaya Khimiya. 62:466-470
Infantile autism is a common disorder of mental development, which is characterized by impairments in the communicative, cognitive and speech spheres and obsessional stereotyped behaviour. Although in most cases, pathogenic factors remain unclear, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::171b5453deae0284a95d2ceec1b87432
https://doi.org/10.18097/pbmc20166204466
https://doi.org/10.18097/pbmc20166204466
Autor:
N. L. Gorbachevskaya, G. V. Kozlovskaya, V. P. Pasekov, N. A. Yegolina, A. B. Sorokin, N. A. Lyapunova, Lev N. Porokhovnik, N. Yu. Korovina, N. K. Sukhotina, T. G. Tzvetkova, N. V. Kosyakova
Publikováno v:
Biology Bulletin Reviews. 4:363-373
Ribosomal genes (RG), or genes for rRNA, are represented by multiple tandem repeats in eukaryotic genomes, and just a part of them is transcriptionally active. The quantity of active copies is a stable genome feature which determines the cell's capab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1966f3b1c5ac1ce3ba938d5cb837c61e
https://doi.org/10.1134/s2079086414050065
https://doi.org/10.1134/s2079086414050065
Autor:
N L Gorbachevskaya, D.S. Pereverzeva, Uliana Mamokhina, Kamilla Danilina, Svetlana Tyushkevich
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 119:103
The objective of this study is to provide a detailed description of clinical characteristics of disorders associated with FMR1 gene, which is located on the long arm of chromosome X. The most frequent FMR1 mutations are related to CGG-repeat expansio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78a034e09694c648e1163e334042c6a1
https://doi.org/10.17116/jnevro2019119071103
https://doi.org/10.17116/jnevro2019119071103
Publikováno v:
Human Physiology. 36:305-311
Three groups of children with LDs (LDs; a total of 62 children) are considered in this study with respect to their specific cognitive and psychological features. In the first group of children, these difficulties are symptoms of the FMR1 gene dysfunc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd6f3d1d910bc2f17d11df4a07a4c380
https://doi.org/10.1134/s0362119710030084
https://doi.org/10.1134/s0362119710030084
Autor:
I.Yu. Yurov, I V Solov'ev, I. A. Demidova, Yu. B. Yurov, V Yu Voinova-Ulas, V.S. Kravets, N. L. Gorbachevskaya, Svetlana G. Vorsanova
Publikováno v:
Neuroscience and Behavioral Physiology. 37:553-558
Cytogenetic and molecular cytogenetic analysis of children with autism (90 subjects) and their mothers (18 subjects) is presented. Anomalies and fragility were found in chromosome X in four cases of autism: mos 47,XXX[98]/46, XX[2]; 46,XY,r(22)(p11q1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cad86addba7d1774d430bbe9cf10f11
https://doi.org/10.1007/s11055-007-0052-1
https://doi.org/10.1007/s11055-007-0052-1
Autor:
Svetlana G. Vorsanova, V.V. Monakhov, A.K. Beresheva, I. A. Demidova, Alexei D. Kolotii, N. L. Gorbachevskaya, Yuri B. Yurov, Viktoria Y Voinova-Ulas, Ivan Y. Iourov, Viktor S. Kravetz
Publikováno v:
Journal of Medical Genetics. 44:521-525
Background: Autism is a common childhood neurodevelopmental disorder with suggested genetic background. About 5-10% of autism cases are associated with chromosomal abnormalities or monogenic disorders. However, the role of subtle genomic imbalances i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52885466161b1fe332d4a0ac0290d032
https://doi.org/10.1136/jmg.2007.049312
https://doi.org/10.1136/jmg.2007.049312