Order results by:
| Issue | Title | |
| 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 12, No 1 (2020) | Association of BAFF gene polymorphisms with multiple sclerosis progression | Abstract PDF (Eng) similar documents |
| I. V. Smagina, S. A. Elchaninova, A. S. Palashchenko | ||
| "... in the pathogenesis of multiple sclerosis (MS). Objective: to analyze the association of BAFF gene polymorphisms (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 ..." | ||
| 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 13, No 1S (2021): Спецвыпуск: рассеянный склероз | Genome-wide polygenic analysis of multiple sclerosis markers | Abstract similar documents |
| Ya. R. Timasheva, T. R. Nasibullin, I. A. Tuktarova, V. V. Erdman, T. R. Galiullin, O. V. Zaplakhova, K. Z. Bakhtiiarova | ||
| "... (PCR) and PCR-restriction fragment length polymorphism analysis of genes of the human leukocyte ..." | ||
| 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 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 14, No 5 (2022) | Study of the role of carriage of single nucleotide variants of the IL-1β, TNFA, BDNF, NTRK-2 genes in the development and clinical features of temporal lobe epilepsy | Abstract PDF (Eng) similar documents |
| Yu. S. Panina, E. A. Domoratskaya, A. I. Paramonova, D. V. Dmitrenko | ||
| "... аллеля А и генотипа GA rs1800629 гена TNFA в развитии ВЭ, генотипа GA rs6265 гена BDNF с развитием ВЭ с ..." | ||
| 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 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) | 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 14, No 5 (2022) | Depression and polymorphism G-174C (rs1800795) of the IL-6 gene in an open population of 25–44 year old in Russia/Siberia (WHO international program MONICA-psychosocial) | Abstract similar documents |
| V. V. Gafarov, E. A. Gromova, D. O. Panov, V. N. Maksimov, I. N. Gagulin, A. V. Gafarova | ||
| "... Objective: to study the association of the G-174C (rs1800795) polymorphism of the IL-6 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 | ||
| 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 11, No 4 (2019) | COMT Val158Met (rs4680) polymorphism and vital exhaustion in an open 45–64-year-old population (international epidemiological WHO MONICA and HAPIEE programs) | Abstract similar documents |
| V. V. Gafarov, E. A. Gromova, D. O. Panov, V. N. Maksimov, I. V. Gagulin, E. A. Krymov, A. V. Gafarova | ||
| "... out a VE scale of the WHO MONICA-psychosocial program. COMT Val158Met (rs4680) 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 | ||
| 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 9, No 2 (2017) | Mental status in pregnant women with brain injury sequels | Abstract similar documents |
| A. A. Volynkin, P. N. Vlasov, V. A. Petrukhin, K. N. Akhvlediani | ||
| "... Objective: to investigate emotional disturbances in pregnant women with sequels of brain injury ..." | ||
| Vol 13, No 2 (2021) | Association of polymorphic marker Val158Met of COMT gene with depression in an open population 25–44 years old (WHO international program MONICA, epidemiological study) | Abstract PDF (Eng) similar documents |
| V. V. Gafarov, E. A. Gromova, D. O. Panov, V. N. Maksimov, I. V. Gagulin, A. V. Gafarova | ||
| "... underwent COMT Val158Met (rs4680) polymorphism genotyping were randomly assigned to a cohort of 224 men ..." | ||
| Vol 13, No 4 (2021) | Methionine synthase reductase A66G polymorphism and ischemic stroke in younger patients | Abstract similar documents |
| O. V. Tsyganenko, L. I. Volkova, A. M. Alasheev | ||
| "... (MTRR) A66G polymorphism is one of the risk factors for ischemic stroke (IS). However, clinical features ..." | ||
| Vol 6, No 2 (2014) | Posttraumatic stress disorder after stroke: rate, risk factors, approaches to prevention and treatment | Abstract similar documents |
| M.A. Kutlubaev, L.R. Akhmadeeva | ||
| Vol 9, No 2 (2017) | The psychological trajectory in a patient with vertebral and spinal cord injury sequels | Abstract similar documents |
| I. D. Boulyubash | ||
| Vol 4, No 1S (2012): Special issue "Epilepsy" | Evolution of a physician’s notion of neonatal seizures and their sequels in the Republic of Tatarstan | Abstract similar documents |
| E. A. Morozova, E. O. Karpova, D. V. Morozov | ||
| Vol 12, No 1S (2020): Спецвыпуск: рассеянный склероз | Polymorphic variants in the PVT1 locus affect multiple sclerosis severity | Abstract PDF (Eng) similar documents |
| I. S. Kiselev, M. S. Kozin, N. M. Baulina, G. V. Pavlova, A. N. Boyko, O. G. Kulakova, O. O. Favorova | ||
| "... polymorphisms for establishing the independence of the observed associations. Patients and methods ..." | ||
| Vol 12, No 1S (2020): Спецвыпуск: рассеянный склероз | The combined effect of nuclear and mitochondrial genomes on the risk of developing multiple sclerosis | Abstract PDF (Eng) similar documents |
| M. S. Kozin, I. S. Kiselev, A. N. Boyko, O. G. Kulakova, O. O. Favorova | ||
| "... of MS with the carriage of biallelic combinations, including as components the polymorphisms of three ..." | ||
| 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 | ||
| "... of the carriage of single nucleotide polymorphisms (SNPs) rs206787 and rs516535 in the BRD2 gene and rs3743123 ..." | ||
| 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 | ||
| "... polymorphisms (SNPs) rs206787 and rs516535 in gene BRD2 and rs3743123 in gene GJD2, from samples of 79 JME ..." | ||
| Vol 14, No 5 (2022) | Association of affective disorders and MTHFR, MTR, and MTRR gene polymorphisms: preliminary results of a family study | Abstract PDF (Eng) similar documents |
| E. D. Kasyanov, T. V. Zhilyaeva, G. E. Maso | ||
| "... Genetic polymorphisms associated with impaired one-carbon metabolism (1-CM) can be a risk factor ..." | ||
| Vol 12, No 3 (2020) | Vitamin D status in patients with multiple sclerosis: an association with insolation, disease course, and HLA-DRB1 gene polymorphism | Abstract PDF (Eng) similar documents |
| I. V. Smagina, K. V. Lunev, S. A. Elchaninova | ||
| "... of vitamin D status in MS patients to insolation, disease course, and HLA-DRB1 gene polymorphism. Patients ..." | ||
| Vol 12, No 1 (2020) | Features of comorbidity of menstrual-related migraine | Abstract similar documents |
| E. A. Kiryanova, G. R. Tabeeva | ||
| Vol 15, No 3 (2023) | Association of the circadian rhythm gene ARNTL/BMAL1 with personal anxiety among people aged 25–64 (WHO international program “MONICA-psychosocial (MOPSY)”) | Abstract PDF (Eng) similar documents |
| V. V. Gafarov, E. A. Gromova, I. V. Gagulin, D. O. Panov, V. N. Maksimov, А. V. Gafarova | ||
| "... Objective: to study associations between personal anxiety (PA) and single nucleotide polymorphism ..." | ||
| Vol 5, No 2S (2013): Special issue "Stroke" | Management of a post-stroke patient | Abstract similar documents |
| Vladimir Anatolyevich Parfenov, S V Verbitskaya | ||
| Vol 12, No 1 (2020) | Analysis of the association of the PRDM12 gene with pain sensitivity in individuals with psychoactive substance dependence | Abstract PDF (Eng) similar documents |
| E. G. Poltavskaya, D. N. Savochkina | ||
| "... was made using a visual analogue scale. Genotyping was performed using the PRDM12 rs10121864 polymorphism ..." | ||
| Online-first | Analysis of the association of the PRDM12 gene with pain sensitivity in individuals with psychoactive substance dependence | Abstract similar documents |
| E. G. Poltavskaya, D. N. Savochkina | ||
| "... the subjective assessment of pain thresholds. Genotyping was performed on the rs10121864 polymorphism of the PRDM ..." | ||
| Vol 13, No 5 (2021) | Association of polymorphic variants of genes (HTR2A, MTNR1A, MTNR1B, CLOCK, DRD2) and insomnia in alcohol dependence syndrome | Abstract PDF (Eng) similar documents |
| I. S. Efremov, A. R. Asadullin, V. S. Dobrodeeva, N. A. Shnayder, E. A. Akhmetova, D. R. Tukhvatullina, E. M. Krupitsky, R. F. Nasyrova | ||
| "... studies on the role of genetic polymorphism of circadian rhythm regulators in sleep disorders in patients ..." | ||
| 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 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 | ||
| Vol 12, No 6 (2020) | The interaction of folate cycle enzyme genes and the risk of extrapyramidal side effects of antipsychotics | Abstract PDF (Eng) similar documents |
| T. V. Zhilyaeva, E. V. Akimova, A. S. Blagonravova, G. E. Mazo | ||
| "... disorders, including single nucleotide polymorphisms (SNPs) in the genes of folate-metabolizing enzymes ..." | ||
| 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 14, No 3 (2022) | Anamnestic, clinical and laboratory features of the acute period of ischemic stroke in young patients | Abstract PDF (Eng) similar documents |
| V. V. Gusev, O. P. Kovtun, O. A. Lvova, E. A. Partylova, A. P. Sergeev, M. V. Sergeeva, I. T. Yanchuk, D. A. Dobrazova, P. A. Suvorkov, N. A. Shamalov | ||
| "... polymorphisms of the thrombophilic spectrum genes were determined – FGB: -455G>A, F2: 20210G>A, F5: 1691G>A, F7 ..." | ||
| Vol 14, No 6 (2022) | Gerstmann–Sträussler–Scheinker syndrome with early-onset spinocerebellar ataxia phenotype | Abstract similar documents |
| E. P. Nuzhnyi, N. Y. Abramycheva, E. Y. Fedotova, S. N. Illarioshkin | ||
| "... changes in the electroencephalography and brain MRI study. The possible modifying role of polymorphism ..." | ||
| Vol 14, No 1 (2022) | COVID-19 associated multiple cranial neuropathies | Abstract similar documents |
| M. Yu. Maksimova, Ya. O. Grusha, E. I. Fettser | ||
| "... The polymorphism of the clinical manifestations of coronavirus infection often creates great ..." | ||
| 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 13, No 3 (2021) | PIP5K2A (rs10828317) polymorphism in patients with alcohol dependence and affective disorders | Abstract PDF (Eng) similar documents |
| E. V. Mikhalitskaya, N. M. Vyalova, O. Yu. Fedorenko, O. V. Roshchina, G. G. Simutkin, N. A. Bokhan, S. A. Ivanova | ||
| "... . Objective: to study the associations of the PIP5K2A (rs10828317) polymorphism with AD and ADs clinical ..." | ||
| Vol 7, No 4 (2015) | Dysphagia after stroke | Abstract similar documents |
| D. O. Gromova, V. V. Zakharov | ||
| "... of the most common sequels of acute cerebrovascular accident. Dysphagia may cause life-threatening ..." | ||
| 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 11, No 2 (2019) | Emotional stress-induced transient global amnesia with bilateral hippocampal ischemic lesion | Abstract similar documents |
| R. Perkovic, K. Buljan, M. Vladetic, F. Katic, S. Misevic, S. Butkovic Soldo | ||
| "... to cope with the sequels of long-term intense stress accompanied with emotion suppression. The described ..." | ||
| Vol 8, No 3 (2016) | Cognitive dysfunction and general anesthesia: From pathogenesis to prevention and correction | Abstract similar documents |
| A. M. Ovezov, M. V. Panteleeva, A. V. Knyazev, A. V. Lugovoy, S. V. Bragina | ||
| "... and correction of POCD is due to its high frequency particularly in elderly patients and to the long-term sequels ..." | ||
| Vol 12, No 4 (2020) | Trigeminal neuropathy following orthognathic surgery | Abstract PDF (Eng) similar documents |
| M. M. Tanashyan, M. Yu. Maksimova, S. Yu. Ivanov, E. M. Musaeva, P. A. Fedin | ||
| "... inferior alveolar neuropathy after corrective mandible surgery is characterized by the polymorphism of pain ..." | ||
| Vol 15, No 6 (2023) | Non-interventional epidemiological program for investigating the real-life practice of using quetiapine (Seroquel®) in patients with schizophrenia and bipolar affective disorder (EPIDEMICUS) | Abstract similar documents |
| V. E. Medvedev, I. G. Kuznetsova | ||
| "... The polymorphism of the clinical manifestations of schizophrenia and bipolar affective disorder ..." | ||
| Vol 8, No 1 (2016) | Factors determining social (interpersonal) support in patients with vertebro-spinal cord injury | Abstract similar documents |
| I. D. Boulyubash, O. S. Bashta | ||
| "... with vertebro-spinal cord injury sequels (VSIS), subjectively perceived and actual social support, and social ..." | ||
| Vol 6, No 4 (2014) | Neurological manifestations of calcific aortic stenosis | Abstract similar documents |
| I. V. Egorov | ||
| "... in patients, but can also be poor prognostic signs. The most common sequels of this disease include heart ..." | ||
| Vol 7, No 1 (2015) | Differential diagnosis of neuropathic pain | Abstract similar documents |
| Yu. N. Bykov, A. N. Kalyagin | ||
| "... and/or central nervous system. Neuropathic pain is a direct sequel of damage to or disease of the somatosensory ..." | ||
| Vol 3, No 2 (2011) | Stroke and cognitive disorders | Abstract similar documents |
| V. V. Zakharov, N. V. Vakhnina | ||
| "... be identified. These include sequels of strategic infarction crucial for cognitive functions; poststroke ..." | ||
| Vol 13, No 5 (2021) | Evaluation of peripheral amyloid neuropathy | Abstract similar documents |
| O. E. Zinovyeva, E. I. Safiulina, N. S. Shcheglova, Z. V. Surnina, A. M. Nosovskiy | ||
| "... . Clinical polymorphism of peripheral somatic and autonomic nervous systems lesions is typical for patients ..." | ||
| Vol 12, No 2 (2020) | Pharmacogenetics of the safety of phenazepam in alcohol withdrawal syndrome: haplotype and combinatorial analyses of polymorphic variants in the pharmacokinetic factor genes | Abstract similar documents |
| D. V. Ivashchenko, O. V. Tereshchenko, I. I. Temirbulatov, K. A. Akmalova, E. A. Grishina, M. S. Zastrozhin, L. M. Savchenko, E. A. Bryun, D. A. Sychev | ||
| "... associations between the CYP3A5, CYP2C9, CYP2C19, CYP2D6 and ABCB1 gene polymorphisms and the safety ..." | ||
| Vol 6, No 2 (2014) | Compensatory and restorative mechanisms in victims in the late postblast period | Abstract similar documents |
| S.M. Karpov, E.M. Bakhadova, A.E. Apaguni, E.N. Karpova | ||
| "... of 27 ageand gender-matched healthy individuals. The trend in BI sequels was traced within 3 years after ..." | ||
| Vol 1, No 1 (2009) | TENOTEN IN COMPLEX THERAPY FOR CEREBROVASCULAR INSUFFICIENCY IN ELDERLY PATIENTS | Abstract similar documents |
| L. D. Serova | ||
| "... of cerebrovascular atherosclerosis, sequels of prior acute ischemic attacks, and posttraumatic encephalopathy ..." | ||
| Vol 15, No 1 (2023) | Association of sleep disorders with various polymorphic variants of the 5-HTTLPR SNP rs25531 A>G gene in people aged 25–44 | Abstract similar documents |
| V. V. Gafarov, E. A. Gromova, I. V. Gagulin, D. O. Panov, V. N. Maksimov, M. A. Gubina, A. V. Gafarova | ||
| "... ,05). Наиболее распространенным генотипом гена 5-HTTLPR SNP rs25531 A>G оказался SLA (43,3%), на втором месте ..." | ||
| Vol 14, No 5 (2022) | Clinical and genetic associations of the CLOCK circadian rhythm gene and depressive disorders in patients with alcohol dependence syndrome during the period of alcohol abstinence | Abstract PDF (Eng) similar documents |
| N. R. Tulbaeva, R. F. Nasyrova, D. A. Smirnova, Z. Sh. Ashurov, I. S. Efremov, V. S. Dobrodeeva, A. E. Abdrakhmanova, A. R. Asadullin | ||
| "... . Обнаружены корреляционные взаимосвязи между носительством генотипа ТТ гена CLOCK у пациентов с алкогольной ..." | ||
| Vol 11, No 4 (2019) | Genetic risk factors for behavioral adverse reactions in epileptic patients taking levetiracetam | Abstract similar documents |
| A. A. Usoltseva, D. V. Dmitrenko, S. N. Zobova, E. N. Bochanova, N. A. Shnayder | ||
| "... ,12 ). Показана статистически значимая ассоциация носительства гетерозиготного генотипа CT ОНВ rs1611115 с ..." | ||
| Online-first | GENETIC RISK FACTORS FOR THE DEVELOPMENT OF BEHAVIORAL ADVERSE DRUG REACTIONS IN PATIENTS WITH EPILEPSY TAKING LEVETIRACETAM | Abstract similar documents |
| A. A. Usoltseva, D. V. Dmitrenko, S. N. Zobova, E. N. Bochanova, N. A. Shnayder | ||
| "... статистически значимая ассоциация носительства гетерозиготного генотипа CT ОНВ rs1611115 с частотой развития как ..." | ||
| 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 ..." | ||
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