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Title
Authors
Vol 7, No 2 (2013)
Current means for identifying the latent stage of a neurodegenerative process
Illarioshkin S.N., Vlassenko A.G., Fedotova E.Y.
PDF
(Rus)
Vol 1, No 4 (2007)
Congenital pathological tortuosity of the internal carotid artery: population screening and genetic aspects
Lobov M.A., Kаzаnchyan P.O., Illarioshkin S.N., Chechetkin A.O., Valikov E.A., Sidorova O.P., Tarаkаnоvа T.Y., Lotareva M.A., Borisova M.N.
PDF
(Rus)
Vol 2, No 2 (2008)
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): first description of a Russian family with the identified mutation in the Notch3 gene
Illarioshkin S.N., Slominsky P.A., Shadrina M.I., Partola M.V., Kandyba D.V., Zhulev N.M.
PDF
(Rus)
Vol 6, No 1 (2012)
Clinical and epidemiological study of the nervous system diseases according to screening of the open population
Varakin Y.Y., Gornostaeva G.V., Manvelov L.S., Konstantinov V.V., Suslina Z.A.
PDF
(Rus)
Vol 16, No 1 (2022)
The Addenbrooke’s Cognitive Examination III (ACE-III): linguistic and cultural adaptation into Russian
Varako N.A., Arkhipova D.V., Kovyazina M.S., Yusupova D.G., Zaytsev A.B., Zimin A.A., Solomina A.V., Bundhun P., Ramchandani N.M., Suponeva N.A., Piradov M.A.
PDF
(Rus)
Vol 12, No 4 (2018)
Identification of Niemann–Pick type C disease in the group of ataxias of unclear origin in adults
Klyushnikov S.A., Proshlyakova T.Y., Baydakova G.V., Nuzhnyi E.P., Nikolaeva N.S., Goncharova Z.A., Fomina-Chertousova N.A., Degtereva E.V., Chernikova V.V., Gorshkova K.V., Artemova N.S., Shperling L.P., Antipova L.N., Tsyplugina O.Y., Ivanova I.L., Chepkasova L.V., Illarioshkin S.N.
PDF
(Rus)
1 - 6 of 6 Items

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