Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Marina Krotenkova"'
Autor:
Natalya V. Ponomareva, Sergey A. Klyushnikov, Natalia Abramycheva, Rodion N. Konovalov, Marina Krotenkova, Ekaterina Kolesnikova, Daria Malina, Gusel Urazgildeeva, Elena Kanavets, Andrey Mitrofanov, Vitaly Fokin, Evgeny Rogaev, Sergey N. Illarioshkin
Publikováno v:
Frontiers in Aging Neuroscience, Vol 16 (2024)
Externí odkaz:
https://doaj.org/article/a39be3539f344a7bab8f7489cbc44a98
Neurophysiological hallmarks of Huntington’s disease progression: an EEG and fMRI connectivity study
Autor:
Natalya V. Ponomareva, Sergey A. Klyushnikov, Natalia Abramycheva, Rodion N. Konovalov, Marina Krotenkova, Ekaterina Kolesnikova, Daria Malina, Gusel Urazgildeeva, Elena Kanavets, Andrey Mitrofanov, Vitaly Fokin, Evgeny Rogaev, Sergey N. Illarioshkin
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
Electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) can provide corroborative data on neurophysiological alterations in Huntington’s disease (HD). However, the alterations in EEG and fMRI resting-state functional connectiv
Externí odkaz:
https://doaj.org/article/ad327d79834744d58c1a750ad857648d
Autor:
Natalya Ponomareva, Tatiana Andreeva, Maria Protasova, Rodion Konovalov, Marina Krotenkova, Daria Malina, Andrey Mitrofanov, Vitaly Fokin, Sergey Illarioshkin, Evgeny Rogaev
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Genome wide association studies (GWAS) have identified and validated the association of the PICALM genotype with Alzheimer’s disease (AD). The PICALM rs3851179 A allele is thought to have a protective effect, whereas the G allele appears to confer
Externí odkaz:
https://doaj.org/article/32ba59e1d8e64f218f92de7bb3a145f0
Autor:
Sofya Morozova, Elena Kremneva, Dmitry Sergeev, Dmitry Sinitsyn, Lyudmila Legostaeva, Elizaveta Iazeva, Marina Krotenkova, Yulia Ryabinkina, Natalia Suponeva, Michael Piradov
Publikováno v:
Brain Sciences, Vol 8, Iss 8, p 144 (2018)
Differential diagnosis of unresponsive wakefulness syndrome (UWS) and minimally conscious state (MCS) is one of the most challenging problems for specialists who deal with chronic disorders of consciousness (DOC). The aim of the current study was to
Externí odkaz:
https://doaj.org/article/7fa8df9fe36e46a1b4d9e1b5144f90de
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 49, Iss 1, Pp 89-97 (2021)
The diagnosis of multiple sclerosis (MS) is quite challenging due to its variable clinical manifestations and lack of a definitive test. Magnetic resonance imaging (MRI) is one of the tools to confirm the diagnosis and also helps in differential diag
Autor:
R. N. Konovalov, Marine M. Tanashyan, O. V. Lagoda, Marina Krotenkova, V. F. Fokin, R. B. Medvedev, N. V. Ponomareva
Publikováno v:
Human Physiology. 46:833-839
Gender differences in cerebral connectivity in subjects with chronic vascular disease are pertinent due to the need for personalized medicine and the theoretical lack of development of the problem. Objective: to analyse the gender differences in neur
Publikováno v:
Human Physiology. 46:845-850
Dissection of the internal carotid (ICA) and vertebral arteries (VA) is one of the most common causes of ischaemic stroke in younger people. Despite wider use of modern neuroimaging techniques in clinical practice, and greater diagnostic capabilities
Autor:
G. R. Urazgildeeva, Anastasia D. Suslina, P. O. Solodchik, O. Dobrushina, Mariia V. Gubanova, G. Arina, Marina Krotenkova, Larisa A. Dobrynina, Elena I. Kremneva, Anastasia V. Belopasova
Publikováno v:
Neuroscience and Behavioral Physiology. 50:1043-1050
Impairments to nociception are currently regarded as the pathogenetic mechanism of psychosomatic disorders and as a potential therapeutic target. An aim of the present work was to investigate the functional cerebral grounds linking the perception of
Publikováno v:
IMMUNO-ONCOLOGY. :79-86
Cerebral venous sinus thrombosis (CVT) becomes the cause of stroke in less than 1% of patients. In 20-30% of patients, the cause of thrombosis remains unclear, and thrombosis is considered idiopathic. Inherited hypercoagulable conditions significantl
Autor:
Zukhra Sh. Gadzhieva, S. N. Morozova, Marina Krotenkova, Larisa A. Dobrynina, O. Dobrushina, Elena I. Kremneva
Publikováno v:
NeuroRegulation. 6:3-14