Zobrazeno 1 - 6
of 6
pro vyhledávání: '"E Iu, Volkova"'
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 108(11)
A history of the discovery, hypotheses of the pathogenesis, neuromorphologic data, clinical appearances, differential diagnostics and an own description of a single case of rare hereditary children leukoencephalopathy, with megalencephaly, changes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::422ce8956913d4b165e778522bca8b68
https://pubmed.ncbi.nlm.nih.gov/19008793
https://pubmed.ncbi.nlm.nih.gov/19008793
Autor:
E Iu, Volkova, M Iu, Bobylova, A A, Alikhanov, S V, Mikhaĭlova, S V, Piliia, M E, Karmanov, G N, Dunaevskaia, E F, Glukhareva
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 108(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c37f24ffb389382240e2358580f30c31
https://pubmed.ncbi.nlm.nih.gov/18646381
https://pubmed.ncbi.nlm.nih.gov/18646381
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
Autor:
R Ts, Bembeeva, Iu V, Mikadze, A S, Petrukhin, T Iu, Gogberashvili, E A, Shakhbazova, I A, Nankina, S V, Piliia, E Iu, Volkova
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 106(12)
Results of the study of cognitive functions in children with multiple sclerosis (MS), including literature data on cognitive disturbances in this disease, are presented. Fourteen patients, aged from 8 to 17 years, with definite MS have been studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b4cf23e1d34e861ffc994f77fb44d17d
https://pubmed.ncbi.nlm.nih.gov/17274390
https://pubmed.ncbi.nlm.nih.gov/17274390
Autor:
K Iu, Mukhin, M B, Muronov, A A, Kholin, L Iu, Glukhova, S V, Piliia, E Iu, Volkova, A L, Golovteev, O A, Pylaeva, A S, Petrukhin
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 106(4)
Fourteen patients, aged from 5 to 14 years, with syndrome of electrical status epilepticus during slow sleep (ESESS) have been studied. The absence of epileptic attacks was observed in 21.5% of patients and diagnosis was established by a combination
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3051e7f380e76bf6347126e8b69062ed
https://pubmed.ncbi.nlm.nih.gov/16737153
https://pubmed.ncbi.nlm.nih.gov/16737153
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 102(2)
The study aimed to differentiate, according to clinical and electroencephalographical criteria, between the most frequent types of myoclonus epilepsy--Unverricht-Lundborg disease (ULD) and Lafora disease (LD). Two patients with ULD and two with LD, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f8c396dd5ba3ae8e1c12937af61531b8
https://pubmed.ncbi.nlm.nih.gov/11915700
https://pubmed.ncbi.nlm.nih.gov/11915700