Zobrazeno 1 - 10
of 183
pro vyhledávání: '"L O, Badalian"'
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 97(1)
The role of functional state of hematoencephalic barrier (HEB) was estimated in terms of development of pathological process in coma. The quantitative determination of neurospecific protein (NSP), exactly of alpha 1 and of alpha 2 cerebral globulins
[Aicardi's syndrome: agenesis of the corpus callosum, infantile flexor spasms and macular dystrophy]
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 96(5)
Autor:
L O, Badalian, M I, Medvedev, A S, Petrukhin, P G, Levin, D A, Kharlamov, M B, Iskander, I N, Bogolepova, E S, Il'ina, S V, Piliia, A A, Alikhanov
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 96(2)
Autor:
L O, Badalian, P A, Temin, M B, Iskander, G N, Dunaevskaia, K Iu, Mukhin, M I, Medvedev, N K, Veselov, V A, Filin, S O, Aĭvazian
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 96(4)
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 96(2)
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 95(5)
The diagnostic value of Lüscher's colour test for the estimation of emotional state of children and juveniles (teenagers) with central nervous system's organic alteration and borderline psychopathological disturbances was analysed. Moreover a number
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 95(4)
Autor:
L O, Badalian, N A, Malygina
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 95(6)
Autor:
L O, Badalian, M I, Medvedev, D A, Kharlamov, P G, Levin, E S, Il'ina, M B, Iskander, M M, Turyleva, A A, Alikhanov
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 95(5)
Observation's analysis of 5 children in age from 9 months to 4 years 11 months with tuberous sclerosis was performed. The initial manifestations of disease were following: early children form of epilepsy exactly infantile spasms (West syndrome) appea
Autor:
A L, Chukhrova, N A, Malygina, A V, Poliakov, S P, Zaĭtseva, V F, Sitnikov, E L, Dadali, L N, Kamennykh, V Iu, Khrennikov, L O, Badalian, O V, Evgrafov
Publikováno v:
TSitologiia i genetika. 28(4)
Patients with Duchenne muscular dystrophy were analyzed using the method of polymerase chain reaction in order to reveal deletions in the dystrophin gene. Deletions of different lengths and locations were detected in 28 of 78 ill boys. The highest nu