Zobrazeno 1 - 9
of 9
pro vyhledávání: '"N. E. Kvaskova"'
MUTATIONS IN THE ARX GENE: CLINICAL, ELECTROENCEPHALOGRAPHIC AND NEUROIMAGING FEATURES IN 3 PATIENTS
Autor:
I. V. Ivanova, K. Yu. Mukhin, O. A. Pylaeva, M. Yu. Bobylova, N. E. Kvaskova, A. S. Petrukhin
Publikováno v:
Русский журнал детской неврологии, Vol 12, Iss 3, Pp 58-67 (2017)
The Aristaless-related homeobox (ARX) gene is a member of the paired-type homeodomain transcription factor family with critical roles in embryonic development, particularly in the developing brain. Mutations in ARX gene demonstrate striking intra- an
Externí odkaz:
https://doaj.org/article/c177bbd0df294fbe8dad389fc9ce27ef
Autor:
M. B. Mironov, V. Iu. Nogovitsyn, M. O. Abramov, E. A. Dobrovskaya, N. E. Kvaskova, K. Yu. Mukhin
Publikováno v:
Эпилепсия и пароксизмальные состояния, Vol 5, Iss 2, Pp 42-46 (2016)
Abstract: Fejerman syndrome (benign nonepileptic myoclonus of infancy) is a rare nonepileptic paroxysmal disorder, characterized by typical presentation of short head nodding or shuddering in otherwise healthy infant without focal signs or psychomoto
Externí odkaz:
https://doaj.org/article/f7e08090fe3a4855b79647656c9b41d3
Autor:
N. E. Kvaskova, K. Yu. Mukhin
Publikováno v:
Русский журнал детской неврологии, Vol 11, Iss 1, Pp 14-22 (2016)
The article presents the clinical, electroencephalographic (EEG) and neuroimaging features, as well as the results of treatment of patients with focal epileptic myoclonus (FEM) with the Kozhevnikov–Rasmussen syndrome (KRS). FEM in KRS-patients was
Externí odkaz:
https://doaj.org/article/2982663ed3dc4dcfb54655d74e1cb9cf
Autor:
K. Yu. Mukhin, N. V. Freidkova, L. Yu. Glukhova, O. A. Pylaeva, M. B. Mironov, N. E. Kvaskova
Publikováno v:
Русский журнал детской неврологии, Vol 10, Iss 4, Pp 7-16 (2016)
Juvenile myoclonic epilepsy (JME) is a type of adolescent-onset idiopathic generalized epilepsy with the appearance of massive myoclonic seizures and, in most cases, generalized convulsions occurring chiefly in the period after awakening. It is assum
Externí odkaz:
https://doaj.org/article/13225f181f2a4b2e9ae34f7a34bd928c
Publikováno v:
Русский журнал детской неврологии, Vol 9, Iss 3, Pp 6-12 (2015)
The paper describes the clinical, electroencephalographic (EEG), and neuroimaging features of focal epileptic myoclonus (FEM) and the results of therapy in patients with this type of seizure. The latter was identified in 2.5 % of the cases of epileps
Externí odkaz:
https://doaj.org/article/aa3bc74f1bc144e897bffe9199cee005
Publikováno v:
Русский журнал детской неврологии, Vol 9, Iss 1, Pp 52-57 (2015)
Kozhevnikov–Rasmussen's encephalitis (KRE) is a rare inflammatory brain disease characterized by severe intractable epilepsy and unilateralprogressive motor defect associated with controlateral hemispheric atrophy. Authors described clinical featur
Externí odkaz:
https://doaj.org/article/c1eb3831090e4d9fab7204035b835e8f
Autor:
K. Y. Mukhin, M. Y. Bobylova, Peter Wolf, M. B. Mironov, Rūta Mameniškienė, Petrukhin As, N. E. Kvaskova
Publikováno v:
Acta Neurologica Scandinavica. 125:345-352
Objectives – Epilepsia partialis continua (EPC) is characterized by localized continuous jerks, from time to time with spreading Jacksonian seizures and, more rarely, secondarily generalized tonic-clonic seizures. EPC has numerous possible etiologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d35a0fc219d7b9225935a5806d8119c
https://doi.org/10.1111/j.1600-0404.2011.01575.x
https://doi.org/10.1111/j.1600-0404.2011.01575.x
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 111(5 Pt 2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::43abe0c9ad3f7de8d8e0ba35076d9374
https://pubmed.ncbi.nlm.nih.gov/23120797
https://pubmed.ncbi.nlm.nih.gov/23120797
Autor:
K Iu, Mukhin, S V, Piliia, E Iu, Volkova, V A, Chadaev, M B, Mironov, N E, Kvaskova, A S, Petrukhin
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 107(3)
An efficacy of high dosages of piracetam in the treatment of children with Kozhevnikov epilepsy syndrome (epilepsia partialis continua) has been studied. The study included 6 patients, aged from 9 to 16 years, with diagnosis of Kozhevnikov epilepsy (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f6d9d7d926fc81d883d2febd249343d
https://pubmed.ncbi.nlm.nih.gov/18379510
https://pubmed.ncbi.nlm.nih.gov/18379510