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Issue Title
 
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 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 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 4, No 1 (2012) Association of the dopamine receptor (DRD4, DAT) gene polymorphisms with vital exhaustion in an open population among 25—64-year-old men (Novosibirsk): Epidemiological study according to the WHO MONICA-psychosocial program Abstract  similar documents
Valery Vasilyevich Gafarov, M I Voyevoda, E A Gromova, V N Maksimov, A V Gafarova, I V Gagulin, N S Yudin, T M Mishakova
"... to estimate the level of vital exhaustion. The examined DRD4, DAT gene Polymorphisms were genotypes ..."
 
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
"... . Genotyping using one single-nucleotide polymorphism was performed in three glutamatergic system genes ..."
 
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 ..."
 
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 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
"... may not be traced in cases of recessive inheritance with a low gene penetrance, as well ..."
 
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 ..."
 
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
"... factors to the development of the disease. The review describes the genes responsible for a predisposition ..."
 
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
"... ) for the clarification of the pathogenetic features and role of neurotrophic factors in the formation of polymorphism ..."
 
Vol 4, No 1S (2012): Special issue "Epilepsy" Clinical and electroencephalographic polymorphism of malignant migrating partial seizures in infancy Abstract  similar documents
A. A. Kholin
"... the UK epilepsy and pregnancy register. Epilepsia 2009;50(Suppl. 4):003. 11. Tomson T., Palm R ..."
 
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 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 ..."
 
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
"... to single-nucleotide polymorphism markers. ..."
 
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
"... an update on the etiology and pathogenesis of this type of glycosphingolipidosis and on established gene ..."
 
Vol 5, No 2S (2013): Special issue "Stroke" Epidemiology and etiology of strokes in babies Abstract  similar documents
Olga Aleksandrovna Lvova, N N Kuznetsov, V V Gusev, S A Volkhina
"... of major thrombophilia gene mutations, may be regarded as a risk group. ..."
 
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
"... and PCDH19 genes, which clinically appears as epileptic seizures, drug-resistant epilepsy, secondary ..."
 
Vol 8, No 1 (2016) Role of lipoprotein (a) in the development of ischemic stroke and other cardiovascular diseases Abstract  similar documents
N. A. Pizov, N. V. Pizova
"... and representatives of other races. There is evidence on the genetic determination and variability of the Apo (a) gene ..."
 
Vol 6, No 2 (2014) A clinical case of SYNGAP1, с2214_2217delTGAG de novo gene mutations in a girl with epilepsy, mental retardation, autism, and movement disorders Abstract  similar documents
M.Yu Bobylova, M.B. Mironov, A.V. Kulikov, M.V Kazakova, M.A. Bogacheva, Yu.A. Tankevich, L.Yu. Glukhova, E.I Barletova, M.O. Abramov, K.Yu. Mukhin, G.E. Rudenskaya
"... clinical case of SYNGAP1, с2214_2217delTGAG de novo gene mutations in a girl with epilepsy, mental ..."
 
Vol 4, No 4 (2012) Coordination function disorders and their evaluation in patients with Chiari malformation type 1 Abstract  similar documents
D N Dunin, Elena Gennadyevna Mendelevich
"... артерий встречались генотипы СС и СТ (p=0,03; ОШ 3,4; ДИ 1,2; 10,2) и аллель С (p=0,02; ОШ 2,7; ДИ 1,2; 6 ..."
 
Vol 4, No 2S (2012): Сognitive and other neuropsychiatric disorders Mental disorders in Huntington’s disease Abstract  similar documents
S. A. Klyushnikov, E. N. Yudina, S. N. Illarioshkin, I. A. Ivanova-Smolenskaya
"... HD gene carriers, by using a battery of psychological tests and the newest methods ..."
 
Vol 10, No 3 (2018) Balo's concentric sclerosis: a clinical case Abstract  PDF (Eng)  similar documents
I. V. Litvinenko, G. N. Bisaga, V. S. Chirsky, R. F. Gimadutdinov, P. S. Dynin, S. Yu. Golokhvastov, V. Yu. Lobzin
"... , there has been a more favorable clinical course of Balo's sclerosis. The significant polymorphism ..."
 
Vol 7, No 1S (2015): Special issue "Epilepsy" A variant of idiopathic epilepsy: Clinical note Abstract  similar documents
V. A. Karlov, S. N. Illarioshkin, G. A. Kovalenko, N. Yu. Abramycheva
"... фенотипом, одинаковой формой эпилептиформной активности во второй стадии сна, одинаковым генотипом у ..."
 
Vol 9, No 1S (2017): SPECIAL ISSUE: EPILEPSY Mechanisms of valproate-induced teratogenesis Abstract  similar documents
D. V. Dmitrenko, N. A. Shnaider, I. G. Strotskaya, A. S. Kichkaylo, S. N. Zobova
"... DV, Shnaider NA. Study of the polymorphism of the CYP2C9 gene in women taking valproate ..."
 
Vol 7, No 2 (2015) Neuromuscular disorders in chronic alcohol intoxication Abstract  similar documents
A. Yu. Emelyanova, O. E. Zinovyeva, N. D. Samkhaeva, N. S. Shcheglova
"... polyneuropathy (PNP) and alcohol-induced skeletal muscle injury. The clinical polymorphism of alcoholic PNP ..."
 
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
"... into epileptic encephalopathies with prolonged spike-wave activity during sleep: the GRIN2A gene encoding ..."
 
Vol 7, No 3 (2015) The late diagnosis of double cortex syndrome in a 36-year-old woman with resistant atonic seizures Abstract  similar documents
N. A. Shnayder, D. V. Dmitrenko, Yu. B. Govorina, E. A. Kantimirova, O. V. Alekseeva, A. A. Molgachev, A. A. Makarkin
"... of 1 to 200,000 people in the population. The cause of the disease is mutation of the gene DCX ..."
 
Vol 6, No 1S (2014): Special issue "Epilepsy" Prevention of Fetal Congenital Malformations with Allowance for the Pharmacogenetic Features of the Metabolism of Antiepileptic Drugs and Hereditary Abnormalities in the Folate Cycle Abstract  similar documents
D. V. Dmitrenko
"... роли полиморфизмов других генов изоферментов CYP450 печени, участвующих в метаболизме ВК [CYP2C9, CYP2A ..."
 
Vol 4, No 1 (2012) Use of Addenbrooke’s cognitive examination-revised to evaluate the patients’ state in general medical practice Abstract  similar documents
Nikolai Nikolayevich Ivanets, D M Tsarenko, M A Bobrova, A A Kursakov, E G Starostina, A E Bobrov
"... жизнен- ного истощения. Генотипирование изучаемых полиморфизмов генов DRD4, DAT проводилось в лаборатории ..."
 
Vol 9, No 1 (2017) The clinical features, diagnosis, and treatment of cognitive impairments in Parkinson's disease Abstract  similar documents
G. N. Akhmadeeva, R. V. Magzhanov, G. N. Tayupova, A. R. Baitimerov
"... study of the influence of COMT gene polymorphism on the nature of the clinical course of Parkinson ..."
 
Vol 7, No 4 (2015) Some aspects of treatment for cognitive impairments. Cyticolin: pharmacological characteristics, possible benefits, aspects of use Abstract  similar documents
N. V. Trofimova, I. S. Preobrazhenskaya
"... 'Aquila P, Rose G, Panno ML, et al. SIRT3 gene expression: a link between inherit- ed mitochondrial DNA ..."
 
Vol 10, No 1S (2018): СПЕЦВЫПУСК: ЭПИЛЕПСИЯ A clinical case of SYNGAP1-associated encephalopathy in a girl with epilepsy, intellectual disability, and autism Abstract  similar documents
N. N. Savelieva, A. V. Yakunina, I. E. Poverennova
"... in  differential diagnosis, since in addition to SYNGAP1 mutation (c2214_2217deltgag), heterozygous BCKDHB gene ..."
 
Vol 8, No 2 (2016) Chronic valproic acid intoxication in epileptology: diagnosis and treatment Abstract  similar documents
N. A. Shnaider, D. V. Dmitrenko
"... важно помнить при лечении паци- енток-носительниц однонуклеотидных полиморфизмов (ОНП) генов фолатного ..."
 
Vol 2, No 3 (2010) Chronic pain Abstract  similar documents
Mikhail Lvovich Kukushkin
"... человека. Современные данные о связи между полиморфизмом генов и особенностями болевой чувстви- тельности ..."
 
Vol 8, No 3 (2016) The role of emotional and behavioral disorders in the development of drug dependence in patients with medication-induced headache (review) Abstract  similar documents
A. E. Shagbazyan, A. V. Sergeev, E. M. Evdokimova, R. R. Kurbanbagamaeva, G. R. Tabeeva
"... ) gene polymorphism influences cortical response to somatosensory stimulation in medication- overuse ..."
 
Vol 9, No 4 (2017) In-hospital stroke in patients after cardiac surgery or invasive interventions Abstract  similar documents
P. A. Filimonova, L. I. Volkova, A. M. Alasheev, A. V. Mikhaylov, E. A. Grichuk
"... grafting is about 2%; that after valve surgery and percutaneous cardiac intervention is 1 to 10% and 0.03 ..."
 
Vol 9, No 3 (2017) Neuroprotective properties of lithium salts during glutamate-induced stress Abstract  similar documents
A. V. Pronin, O. A. Gromova, I. Yu. Torshin, E. V. Stelmashuk, O. P. Aleksandrova, E. E. Genrikhs, L. G. Khaspekov
"... increased the survival rate of CGNs by an average of 30% (p < 0.003). The active neuroprotective principles ..."
 
Vol 10, No 4 (2018) Environmental factors and a risk for multiple sclerosis in the Altai Territory Abstract  similar documents
I. P. Saldan, I. V. Smagina, S. A. Elchaninova
"... and towns than in villages (p=0.003), in areas with heavy metal (lead and molybdenum) ore deposits, chemical ..."
 
Vol 7, No 3 (2015) Hereditary cerebellar ataxias with polyneuropathy Abstract  similar documents
Svetlana Vasilyevna Kopishinskaya
"... ataxia. A mutant gene and concurrent symptoms are indicated. The differential diagnosis of cerebellar ..."
 
Vol 7, No 4 (2015) Migraine and hypertension Abstract  similar documents
G. R. Tabeeva, A. V. Muranova, E. N. Kostrygina, A. V. Sergeev
"... гиперлипидемией [6]. На основании этих результатов можно предположить роль специфических генотипов, связанных с ..."
 
No 1S (2016): Clinical and electroencephalographic characteristics of chronic tic disorders in children and adolescents Abstract  similar documents
N. A. Ermolenko, E. I. Zakharova, I. A. Buchneva
"... больше (p=0,003) детей с изолированными моторными тиками в области лица в I группе – 24,1% (n=13) против ..."
 
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
"... генотипом АРОЕ и холинерги- ческим дефицитом при БА: снижение активности ацетилхолинтрансферазы в гиппокампе ..."
 
Vol 4, No 1 (2012) Weather risk factors for stroke in the Central Region of Russia Abstract  similar documents
Natalia Vyacheslavovna Pizova, S D Prozorovskaya, A V Pizov
"... T., Harms H., Podschus J. et al. Allelic association of a dopamine transporter gene polymorphism in ..."
 
Vol 5, No 3 (2013) Lower back pain: Therapy in the context of evidence-based medicine and new possibilities Abstract  similar documents
Aleksei Vladimirovich Sergeev
"... ]. Установлена достоверная ассоциация ме- жду полиморфизмом в системе гена интерлейкина 1 и деге- неративно ..."
 
Vol 7, No 2 (2015) Gender features of depressive disorders in women Abstract  similar documents
N. A. Tyuvina, V. V. Balabanova, E. O. Voronina
"... различий начинается уже в развивающемся эмбрионе. У плода с генотипом ХY в корот- ком плече хромосомы Y ..."
 
Vol 4, No 4 (2012) Current approaches to preventing and treating chronic cerebral circulatory disorder Abstract  similar documents
Marina Yuryevna Maksimova, M A Domashenko, M M Tanashyan
"... polymorphism associated with post-stroke major depression. J Neuropsychiatry Clin Neurosci 2006;18:96–9. 18 ..."
 
Vol 6, No 2S (2014): Special issue "Stroke" Drug therapy and cognitive stimulation in patients with poststroke cognitive impairments Abstract  similar documents
D.R. Khasanova, Yu.V. Zhitkova, L.M. Yu.V.
"... комбинированную стимуля- цию нейрональной пластичности (р=0,003). Те же тенденции наблюдались при оценке по ШЛД ..."
 
Vol 8, No 2 (2016) Histological classification of mesial temporal sclerosis Abstract  similar documents
D. V. Dmitrenko, M. A. Stroganova, N. A. Shnaider, G. P. Martynova, K. A. Gazenkampf, A. V. Dyuzhakova, Yu. S. Panina
"... феб- рильных приступов и височной эпилепсии [13]. Установлено, что генотип ApoEε4 связан с повышенным ..."
 
Vol 4, No 2S (2012): Сognitive and other neuropsychiatric disorders Long-term therapy for polymorphic mental disorders in liquidators of the consequences of the accident at the Chernobyl nuclear power plant Abstract  similar documents
V. N. Krasnov, V. V. Kryukov, I. N. Emelyanova, N. Ya. Kurmysheva, M. M. Yurkin, I. A. Ryzhova, E. F. Samedova
"... с гормональными и обменными дисфункциями. Полиморфизм выявляемых расстройств изначально затруднял ..."
 
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