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Vol 6, No 1S (2014): Special issue "Epilepsy" Genetics of Epilepsy: What for and How to Examine Children with Epilepsy E.D. Belousova Abstract  similar documents
E. D. Belousova
"... The paper focuses on problems of genetic examination of children with epilepsy. The major types ..."
 
Vol 7, No 1 (2015) Time course of changes in the development of gait disorders in multiple sclerosis Abstract  similar documents
A. M. Petrov, I. D. Stolyarov, G. G. Shkilnyuk, A. G. Ilves, K. K. Mineev, V. V. Lebedev, T. L. Tsvetkova
"... was evaluated using the expanded disability status scale (EDSS); pedographic examination was made applying ..."
 
Vol 2, No 1 (2010) VASCULAR DEMENTIA Abstract  similar documents
M. A. Cherdak, O. V. Uspenskaya
"... for the examination and treatment of patients with vascular cognitive disorders and vascular dementia (VD ..."
 
Vol 2, No 1 (2010) NEUROPSYCHOLOGICAL SYNDROMES OF HIGHER PSYCHIC FUNCTIONS IN CHILDREN AND ADOLESCENTS WITH FOCAL FORMS OF EPILEPSY Abstract  similar documents
Yu. V. Mikadze, T. Yu. Gogberashvili
"... neuropsychological examination of HPF developed by A.R. Luria and his followers was performed in children ..."
 
Vol 6, No 4 (2014) The epidemiological, clinical, and genetic characteristics of Parkinson’s disease (in case of Zheleznogorsk) Abstract  similar documents
M. R. Sapronova, N. A. Shnaider
"... genetic examination; 3) 30 healthy volunteers (66.7% of women and 33.3% of men) – a control group ..."
 
Vol 11, No 2 (2019) Tobacco smoking dependence in patients with depressive spectrum mental disorders: clinical, pathogenetic, and therapeutic aspects Abstract  similar documents
O. I. Speranskaya, S. A. Trushchelev, Z. I. Storozheva
"... established to be to a large extent determined by their common genetic bases. This association substantially ..."
 
Vol 11, No 3 (2019) Mitochondrial genome and risk of multiple sclerosis Abstract  similar documents
A. N. Boyko, M. S. Kozin, G. Zh. Osmak, O. G. Kulakova, O. O. Favorova
"... Mitochondrial DNA (mtDNA) polymorphism makes a certain contribution to the formation of a genetic ..."
 
Vol 8, No 4 (2016) INTERMEDIATE PHENOTYPES OF OBSTRUCTIVE SLEEP APNEA/HYPOPNEA SYNDROME Abstract  similar documents
N. A. Shnayder, M. M. Petrova, I. V. Demko, O. V. Alekseeva
"... phenotypes of OSAHS, in the development of which there may be a genetic component. It is stated that a study ..."
 
Vol 11, No 4 (2019) Prognostic significance of moderate cognitive impairment in patients at high and very high cardiovascular risk Abstract  similar documents
V. V. Henkel, A. S. Kuznetsova, A. O. Salashenko, E. V. Lebedev, I. I. Shaposhnik
"... the Mini-Mental State Examination (MMSE) scale in patients at high and very high cardiovascular risk (CVR ..."
 
Vol 10, No 3 (2018) Cognitive impairment in patients with migraine: causes, principles of effective prevention and treatment Abstract  similar documents
V. A. Golovacheva, K. A. Pozhidaev, A. A. Golovacheva
 
Online-first Association of carriers of single nucleotide polymorphisms rs206787 and rs516535 in gene BRD2 and rs3743123 in gene GJD2 with juvenile myoclonic epilepsy of Caucasian patients in the Siberia Abstract  similar documents
O. S. Shilkina, N. A. Shnayder, S. N. Zobova, D. V. Dmitrenko, P. V. Moskaleva
"... This article outlines recent findings on genetics of juvenile myoclonic epilepsy (JME), where JME ..."
 
Vol 11, No 4 (2019) Association of the carriage of BRD2 rs206787 and rs516535 and GJD2 rs3743123 polymorphisms with juvenile myoclonic epilepsy in Caucasian patients of Siberia Abstract  similar documents
O. S. Shilkina, N. A. Shnayder, S. N. Zobova, D. V. Dmitrenko, P. V. Moskaleva
"... In recent years, the genetics of juvenile myoclonic epilepsy (JME) has been actively studied ..."
 
Vol 10, No 4 (2018) Use of valproate and carbamazepine in the therapy of epilepsy (guidelines for the practitioner) Abstract  similar documents
P. N. Vlasov
 
Vol 5, No 4 (2013) A case of Niemann – Pick disease type C Abstract  similar documents
Sergei Anatolyevich Klyushnikov, O R Smirnov, E Yu Zakharova
"... diagnostic verification, including molecular genetic testing, are presented. Information is given on specific ..."
 
Vol 6, No 4 (2014) The development and treatment of Alzheimer’s disease: Some genetic aspects Abstract  similar documents
I. S. Preobrazhenskaya, N. S. Snitskaya
"... . The reason for its higher incidence rate is the specific features of the current information sphere. Genetic ..."
 
Vol 9, No 1S (2017): SPECIAL ISSUE: EPILEPSY A clinical case of epilepsy in a female patient with double mutations in the SCN2A and PCDH19 genes Abstract  similar documents
M. B. Mironov, M. Yu. Bobylova, S. G. Burd, T. M. Krasilshchikova, M. M. Gunchenko, M. N. Sarzhina, T. T. Batysheva
 
Vol 8, No 3 (2016) A clinical case of adult onset Niemann–Pick disease type C Abstract  similar documents
E. V. Saifullina, R. V. Magzhanov, A. K. Mardanova, T. Yu. Proshlyakova, E. Yu. Zakharova, S. A. Klyushnikov, S. N. Illarioshkin
 
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