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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
"... 16944 and rs1143634 of the IL1B gene and rs6265 of the BDNF gene with the development of temporal lobe ..."
 
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
"... SNPs rs16944, rs1143634 of IL-1B gene and rs6265 of BDNF gene in the development of TLE. Patients ..."
 
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
"... the association of the carriage of the SNPs rs16944 and rs1143634 in the IL-1B gene and rs6265 in the BDNF gene ..."
 
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 the polymorphic variants of glutamatergic system genes, such as GRIN2A encoding the N-methyl-D-aspartate (NMDA ..."
 
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
"... Objective: to study the association of the DRD4, DAT genes with vital exhaustion in an open 25—64 ..."
 
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 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 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 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 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
"... мутации гена SYNGAP1, с2214_2217delTGAG de novo у девочки с эпилепсией, ум- ственной отсталостью ..."
 
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 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 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 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 5, No 3 (2013) Diabetic peripheral neuropathy therapy-induced activation of humoral serotonin and endogenous neurotrophins Abstract  similar documents
Yuulia Vladimirovna Karakulova, N B Kaigorodova, E A Batueva
"... platelets, and the levels of brain-derived neurotrophic factor (BDNF) and nerve growth factor were studied ..."
 
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 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 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
"... doses of SV. The frequency of the CYP2C9 gene among SNPs proved to be highest: CYP2C9*1/*1 in 68 (72 ..."
 
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 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 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
"... Цель исследования – изучение ассоциации полиморфизма гена DRD2/ANKK1 Taq1A с депрессией в открытой ..."
 
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 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
"... экзоне гена LRRK2, играющей роль в развитии как моногенных, так и спорадических случаев БП. В статье ..."
 
Vol 11, No 1 (2019) Efficiency of long-term vinpocetine administration in the treatment of dizziness and associated statodynamic disorders in patients with chronic cerebrovascular insufficiency (EDELWEISS study) Abstract  similar documents
I. N. Samartsev, S. A. Zhivolupov, Yu. S. Butakova, M. V. Morozova, I. N. Barsukov
"... brain-derived neurotrophic factor (BDNF) concentrations were analyzed before and after treatment ..."
 
Vol 7, No 4 (2015) Neurotrophic and antioxidant potential of neuropeptides and trace elements Abstract  similar documents
O. A. Gromova, A. V. Pronin, I. Yu. Torshin, A. G. Kalacheva, T. R. Grishina
"... (NGF), нейротрофический фактор мозгового происхожде- ния (BDNF), нейротрофины (NT-3, NT-4/5, NT-6 ..."
 
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
"... инвертированный повтор разме- ром 500 тыс пар нуклеотидов, содер- жащий 4 гена: SMN, NAIP, SERF1A(H4F5) и GTF2H2 ..."
 
Vol 1, No 1 (2009) THE ACUTE PERIOD OF ISCHEMIC STROKE: DIAGNOSIS AND TREATMENT Abstract  similar documents
V A Parfenov, V A Parfenov
"... экспрессия гена 11β-гидроксистероидной дегидрогеназы 2 типа. Назначение ГК беременным для обеспечения ..."
 
Vol 4, No 2S (2012): Сognitive and other neuropsychiatric disorders Cognitive and emotional impairments in men and women with dyscirculatory encephalopathy Abstract  similar documents
Y. V. Abramenko, N. A. Yakovlev
"... эндо- генного BDNF для обучения и памяти животных: введение BDNF в гиппокамп крыс улучшало ..."
 
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
"... с микротру- бочками (MAPT) [23] или полиморфизм Val66Met гена BDNF – нейротрофического фактора ..."
 
Vol 10, No 1S (2018): СПЕЦВЫПУСК: ЭПИЛЕПСИЯ The role of neuroinflammation in the pathogenesis of epilepsy Abstract  similar documents
L. V. Lipatova, N. B. Serebryanaya, N. A. Sivakova
"... factor (BDNF), S100b protein, С-reactive  protein (CRP), and albumins were analyzed using a solid-phase ..."
 
Vol 8, No 1 (2016) Synergistic neurotrophic effects of piracetam and thiotriazoline Abstract  similar documents
O. A. Gromova, I. Yu. Torshin, A. V. Pronin, A. Yu. Volkov
"... -рецепторов повы- шает экспрессию мозгового нейротрофического фактора (BDNF) за счет модуляции ..."
 
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
"... острие научного дис- курса – ингибирование гистондеацетилазы [5] с антиангио- генным эффектом [6 ..."
 
Vol 4, No 2 (2012) Strokes in mitochondrial diseases Abstract  similar documents
N V Pizova
"... имеется ассоциация с мутацией гена tRNALeu (UUR, включая 3243A > G [8], 3251A > G [9], 3252T > C [10] и ..."
 
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
"... четко определенными факторами риска развития БА. В настоящее время известны че- тыре основные генные ..."
 
Vol 8, No 2 (2016) The peripheral and central mechanisms of transition of acute to chronic pain and the possible role of cyclooxygenase-2 inhibition in the prevention of pain syndrome chronization Abstract  similar documents
O. S. Davydov
"... (посттрансляционные изменения), во второй – экспрессия генов белков, приводя- щая к выработке новых белков ..."
 
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
"... этом белке немного [23]. Ген SIRT3 у человека содер- жит тандемные повторы с переменным числом звеньев ..."
 
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
"... ассоциации между -5Т/С-полимор- физмом гена GP1BA и ИИ указывают на то, что этот поли- морфизм ассоциирован ..."
 
Vol 8, No 2 (2016) Psychogenic dizziness Abstract  similar documents
L. M. Antonenko
"... системой поддержания равновесия. При психо- генном головокружении иллюзия движения может быть результатом ..."
 
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
"... ]. Тип передачи мутантного гена – аутосомно-рецессивный, в подавляющем большинстве случаев (около 95 ..."
 
Vol 9, No 1 (2017) The triple synergy of ethylmethylhydroxypyridine succinate, magnesium, and vitamin B6: Molecular mechanisms Abstract  similar documents
O. A. Gromova, A. G. Kalacheva, I. Yu. Torshin, T. R. Grishina, I. K. Tomilova
"... активностей соответст- вуют определенные гены из генома человека (табл. 1). Сравнение данных о генах ..."
 
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
"... [18]. Ферменты, ответственные за метаболизм АЭП, и поли- морфные аллельные варианты генов, их ..."
 
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
"... ассоциации генов DRD4, DAT с жизненным истощением в открытой популяции мужчин 25–64 лет. В рамках программы ..."
 
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 6, No 3 (2014) Alcohol abuse and related disorders treatment of alcohol dependence Abstract  similar documents
Yu. P. Sivolap
"... - derived neurotrophic factor – BDNF), возрастающей под вли- янием мемантина в некоторых отделах мозга ..."
 
Vol 8, No 4 (2016) MexiB 6 AS A RESULT OF FORTIFICATION OF ETHYLMETHYLHYDROXYPYRIDINE SUCCINATE WITH MAGNESIUM AND PYRIDOXINE: PROTEOME EFFECTS Abstract  similar documents
O. A. Gromova, I. Yu. Torshin, A. G. Kalacheva, V. A. Semenov, K. V. Rudakov
"... эффекты пиридоксина и магния в рамках постгеномной медицины: воздействие на геном (со- вокупность всех ..."
 
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
"... +5 G→A в гене, кодирующем α -субъединицу нейронального натриевого канала, ас- социируемого с ..."
 
Vol 6, No 1 (2014) Dementia of the Alzheimer type: current state of the problem Abstract  similar documents
N.A. Tyuvina, V.V. Balabanova
"... - щенная деменцией альцгеймеровского типа наследствен- ность, наличие определенных аллелей в генах. Во ..."
 
Vol 4, No 2 (2012) Capacities of the dopamine receptor agonist pramipexole in the treatment of patients with Parkinson’s disease Abstract  similar documents
S N Illarioshkin
"... missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome. Neurology ..."
 
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