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Neurology, Neuropsychiatry, Psychosomatics

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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 ..."
 
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 9, No 1 (2017) The genetic basis of Parkinson's disease Abstract  similar documents
A. A. Tappakhov, T. E. Popova, T. Ya. Nikolaeva, P. I. Gurieva, N. A. Shnaider, M. M. Petrova, M. R. Sapronova
"... Parkinson's disease (PD) is a multifactorial disease that develops in the presence of both genetic ..."
 
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
"... consideration is being given to a search for genetic markers for the LRRK2 6055G>T mutation in exon 41, which ..."
 
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 4, No 4 (2012) Analysis of the contribution of -5t/c polymorphism in the GP1BA gene to the development of ischemic stroke in young patients Abstract  similar documents
V I Skvortsova, E A Koltsova, Ekaterina Igorevna Kimelfeld, S A Limborskaya, P A Slominsky, T V Tupitsyna
"... The impact of -5T/C polymorphism in the GP1BA gene on the risk of ischemic stroke (IS) was studied ..."
 
Vol 8, No 1 (2016) SNAP-25 gene polymorphism and cognitive resource in patients with stroke sequels Abstract  similar documents
V. B. Vilyanov, G. N. Kobozev
"... Objective: to determine the impact of SNAP-25 gene polymorphisms on the cognitive potential ..."
 
Vol 9, No 1 (2017) Clinical and biochemical polymorphism of spinal muscular atrophy Abstract  similar documents
M. G. Sokolova, S. V. Lobzin, I. V. Litvinenko, M. V. Rezvantsev, L. A. Polyakova
"... be explained by the polymorphism of various pathogenic factors: genetic, morphofunctional, and biochemical ones ..."
 
Vol 10, No 1 (2018) G308A tumor necrosis factor-α gene polymorphism and depression in an open male population aged 25–64 years from Novosibirsk (an epidemiological study according to the WHO MONICA-psychosocial program) Abstract  similar documents
I. V. Gagulin, E. A. Gromova, A. V. Gafarova, V. V. Gafarov
"... ) gene polymorphism with depression in an open male population aged 25–64 years in Novosibirsk. Patients ..."
 
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 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 ..."
 
Online-first Association of carriers of single nucleotide polymorphisms rs1143634 and rs16944 in gene Il-1B and rs6265 in gene BDNF with temporal lobe epilepsy Abstract  similar documents
Y. S. Panina, D. V. Dmitrenko, N. A. Shnayder, E. V. Egorova, A. A. Usoltseva
"... neurotrophic factor (BDNF) may be associated with the carriage of the single nucleotide polymorphism (SNP) rs ..."
 
Vol 11, No 2 (2019) Association of DRD2/ANKK1 Taq1A polymorphism with depression in an open 45–64 year-old male population (international epidemiological HAPIEE and WHO MONICA programs) Abstract  PDF (Eng)  similar documents
V. V. Gafarov, E. A. Gromova, D. O. Panov, V. N. Maximov, I. V. Gagulin, A. V. Gafarova
"... Objective: to study the association of DRD2/ANKK1 Taq1A polymorphism with depression in an open 45 ..."
 
Vol 11, No 2 (2019) Association of the carriage of IL-1B rs1143634 and rs16944 polymorphisms and BDNF rs6265 polymorphism with temporal lobe epilepsy Abstract  PDF (Eng)  similar documents
Yu. S. Panina, D. V. Dmitrenko, N. A. Shnaider, E. V. Egorova, A. A. Usoltseva
"... polymorphism (SNP) rs6265 in the BDNF gene. Groups of investigators have shown the increased expression of BDNF ..."
 
Online-first Association of carriers of single nucleotide polymorphisms rs1143634 and rs16944 of the Il-1B gene and rs6265 of the BDNF gene with temporal lobe epilepsy Abstract  similar documents
Y. S. Panina, D. V. Dmitrenko, N. A. Shnayder, E. V. Egorova, A. A. Usoltseva
"... nucleotide polymorphism (SNP) of the rs6265 BDNF gene. The research groups have shown increased expression ..."
 
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 10, No 2 (2018) Parkinson's disease and polymorphisms of the glutamatergic system genes GRIN2A, SLC1A2, and GRIK4 Abstract  similar documents
Yu. S. Mironova, I. A. Zhukova, N. G. Zhukova, S. A. Ivanova, V. M. Alifirova, A. S. Boiko, D. Z. Osmanova, O. P. Izhboldina, A. V. Latypova
"... with multi-neurotransmitter dysfunction, so it is important to search for genetic risk factors that determine ..."
 
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
"... mutations. The clinical polymorphism of NPC and the trends in the development of somatic, mental ..."
 
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
 
Vol 9, No 1S (2017): SPECIAL ISSUE: EPILEPSY The efficacy and safety of valproic acid medications with controlled active ingredient release in adults in real clinical practice from the position of pharmacokinetic and pharmacogenetic approaches Abstract  similar documents
P. N. Vlasov, N. V. Orekhova, M. V. Antonyuk, N. V. Filatova, N. A. Schnaider, D. V. Dmitrenko, S. N. Zobova, I. E. Poverennova, A. V. Yakunina, V. A. Kalinin, S. K. Zyryanov, I. F. Tishchenkova
"... polymorphisms (SNPs) CYP2C9*3 (27.3%) versus those who had the common (wild-type) allele variant CYP2C9*1 ..."
 
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