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Issue Title
 
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 ..."
 
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 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 ..."
 
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 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 ..."
 
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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 4, No 1S (2012): Special issue "Epilepsy" Clinical and electroencephalographic polymorphism of malignant migrating partial seizures in infancy Abstract  similar documents
A. A. Kholin
"... Александрович Холин drkholin@mail.ru Clinical and electroencephalographic polymorphism of malignant migrating ..."
 
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
"... ., Li C.Q., Khoshnevis- Asl M. et al. Kozak sequence polymorphism of the glycoprotein (GP) Ibalpha 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 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 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 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 7, No 3 (2015) Treatment for Alzheimer's diseases Abstract  similar documents
Nina Arkadyevna Tyuvina, V. V. Balabanova
"... определенных аллелей в генах. Обсу- ждается значение сосудистых факторов, в частности повыше- ния артериального ..."
 
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
"... плазме крови. Носительство «быстрого» аллель- ного варианта гена CYP2C19*17 (c. 806 С>Т и с. 3402 С>Т) со ..."
 
Vol 7, No 3 (2015) The heterogeneity of vascular cognitive impairments and the issues of therapy Abstract  similar documents
Elena Anatolyevna Katunina
"... оказывать влияние на развитие сосудистых КН. Наличие аллеля ε4 гена аполи- попротеина Е повышает риск ..."
 
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 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 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 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
"... высоким уровнем жизненного истощения достоверно ассоциирован генотип, содержащий аллель 7 гена ..."
 
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 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 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 7, No 3 (2015) Experience in using levodopa-benserazide Abstract  similar documents
Elena Anatolyevna Katunina, Yu. N. Bezdolnyi, E. A. Malykhina, N. V. Titova
"... дис- кинезий пика дозы. Наличие аллеля rs4704559G в гене HOMER 1 ассоциируется со снижением частоты ..."
 
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 7, No 4 (2015) Migraine and hypertension Abstract  similar documents
G. R. Tabeeva, A. V. Muranova, E. N. Kostrygina, A. V. Sergeev
"... нарушение активности системы кальцитонин-ген-родст- венного пептида, участвующего в развитии приступа мигре ..."
 
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 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 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 3, No 4 (2011) New criteria for diagnosing Alzheimer's disease Abstract  similar documents
Andrei Yuryevich Emelin
"... функциональную МРТ, могут быть информативными на ранних стадиях, особенно при наличии изоформы гена apoЕ4; 3 ..."
 
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 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 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 7, No 3 (2015) A clinical case of a patient with probable cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) from Chuvashia Abstract  similar documents
Tatiana Vladimirovna Mokina, A. V. Zvereva, Yu. I. Pavlov, N. K. Sumkin, T. V. Karpova
"... -доминантный. Оба пола поража- ются в одинаковой степени. Заболевание обусловлено мута- цией гена Notch3 ..."
 
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