Neurology, Neuropsychiatry, Psychosomatics

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Issue Title
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 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 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 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 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 ..."
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
"... ARs. Objective: to establish genetic risk factors for behavioral ADRs in epileptic patients taking ..."
Yu. V. Zhitkova, A. A. Gasparyan, D. R. Khasanova, N. R. Khasanov, V. N. Oslopov
"... различных сосудистых бассейнах. Выявлена взаимосвязь показателя ЦВР с генетически детерминированным уровнем ..."
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
A. A. Usoltseva, D. V. Dmitrenko, S. N. Zobova, E. N. Bochanova, N. A. Shnayder
"... of LEV-induced ADR. Purpose: To determine the genetic risk factors for the development of behavioral ADR ..."
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 5, No 4 (2013) A case of Niemann – Pick disease type C Abstract  similar documents
Sergei Anatolyevich Klyushnikov, O R Smirnov, E Yu Zakharova
"... diagnostic verification, including molecular genetic testing, are presented. Information is given on specific ..."
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 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
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 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
"... The practical introduction of the latest genetic techniques could provide the basis ..."
Vol 7, No 3 (2015) Hereditary cerebellar ataxias with polyneuropathy Abstract  similar documents
Svetlana Vasilyevna Kopishinskaya
"... by molecular genetic testing. In recent years, some genetic diseases manifesting themselves by a concurrence ..."
E. V. Malinina, S. A. Suprun, E. A. Markova
"... on the implication of genetic and organic disorders and epileptiform activity in the origin of these disorders ..."
Vol 10, No 1S (2018): СПЕЦВЫПУСК: ЭПИЛЕПСИЯ Unverricht-Lundborg disease in an adult female patient: a clinical case Abstract  similar documents
V. A. Karlov, I. A. Zhidkova, E. Yu. Mishina, P. N. Vlasov, N. V. Margosyuk, L. P. Tingaeva, E. M. Perepelova, V. A. Perepelov, B. P. Gladov, S. A. Trukhanov
"... been long followed up for diagnosed juvenile myoclonic epilepsy); the relative role of a genetic study ..."
Vol 5, No 3 (2013) Two cases of Wilson–Konovalov disease Abstract  similar documents
Alla Anatolyevna Strutsenko, V V Golubeva, N V Mazurchik, N I Garabova, N V Nozdryukhina
"... genetic disorder. For its pathogenesis, there is the underlying genetic disorder of copper metabolism ..."
Vol 11, No 3S (2019): Спецвыпуск: когнитивные нарушения, цереброваскулярные заболевания Alzheimer's disease Abstract  similar documents
N. N. Koberskaya
"... Despite progress made in laboratory methods, genetic studies, and modern neuroimaging ..."
Vol 11, No 3 (2019) Vascular cognitive impairment and Alzheimer's disease: Is there a relationship between them? Abstract  similar documents
G. R. Tabeeva, E. A. Kirjanova
"... manifestations, neuromorphological changes, as well as genetic and neuroimaging biomarkers. The complex ..."
Vol 9, No 4 (2017) Neuropsychological pattern of Parkinson's disease Abstract  similar documents
A. A. Tappakhov, T. E. Popova, T. Ya. Nikolaeva, N. A. Schnaider, M. M. Petrova, M. R. Sapronova
"... of and diagnostic criteria for impulsivecompulsive disorders in PD and the contribution of genetic ..."
Vol 9, No 3 (2017) Current views of the risk factors, diagnosis, and therapy of Alzheimer's disease (according to the proceedings of the Alzheimer's Association International Conference, London, 2017) Abstract  similar documents
N. N. Koberskaya
"... in the elderly. The data of epidemiological and genetic studies and risk factors for AD were considered. Great ..."
Vol 4, No 1 (2012) Generalized epilepsies: current conceptions and therapeutic approaches Abstract  similar documents
L R Zenkov
"... epilepsies have been revealed. The closeness of these forms is also supported by genetic studies when one ..."
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 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
"... system, the risk of which depends on genetic and environmental factors. The Altai Territory ..."
Vol 10, No 4 (2018) Research Institute of Internal and Preventive Medicine, Branch, Federal Research Center, Institute of Cytology and Genetics, Siberian Branch, Russian Academy of Sciences Abstract  similar documents
A. V. Titarenko, S. V. Shishkin, L. V. Shcherbakova, E. G. Verevkin, M. Holmes, M. Bobak, S. K. Malyutina
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
"... in the Laboratory of Molecular Genetic Studies, Therapy Research Institute, Siberian Branch, Russian Academy ..."
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
"... ) along with individual genetic characteristics, environmental factors, and lifestyle, each of which has ..."
Vol 4, No 4 (2012) Poststroke depression: prevalence, pathogenesis, diagnosis, and treatment Abstract  similar documents
Vladimir Anatolyevich Parfenov
"... of psychological factors, genetic predisposition, brain lesion location, monoamine deficiency in the pathogenesis ..."
Vol 8, No 2 (2016) Alzheimer's disease under the mask of stroke Abstract  similar documents
A. A. Naumenko, N. V. Vakhnina
"... , cerebrospinal fluid examination, and genetic testing are used to reveal AD at its preclinical stages. Preventive ..."
Vol 6, No 4 (2014) Cognitive impairments in cerebrovascular disease Abstract  similar documents
A. Yu. Emelin
"... cognitive impairments (VCI). The etiological factors of VCI may be divided into genetic, sociodemographic ..."
Vol 6, No 4 (2014) The specific features and pattern of febrile infection-related epilepsy syndrome (FIRES) in children Abstract  similar documents
L. V. Shalkevich, O. A. Lvova, A. I. Kudlach, V. V. Komir
"... of FIRES, such as metabolic, genetic, and immunological disorders, aseptic inflammatory processes, as well ..."
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 9, No 1 (2017) Clinical and epidemiological features of patients with multiple sclerosis in the Kursk Region Abstract  similar documents
V. B. Laskov, E. A. Logacheva, E. E. Tretyakova, M. A. Gridnev
"... ) and urban residence; the role of genetic characteristics and exposure to pesticides and industrial allergens ..."
Vol 9, No 3 (2017) A chronobiological approach to therapy for depression Abstract  similar documents
M. Yu. Gerasimchuk
"... of the existing genetic predisposition increases a risk for the occurrence and chronicity of depression. To solve ..."
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 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
"... genetic study of the carriage of the SNPs rs1143634 and rs16944 in the IL-1B gene and rs6265 in the 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
"... epilepsy. Patients and methods. We carried out a molecular genetic study of the carrier of SNPs rs1143634 ..."
Vol 8, No 2 (2016) Chronic valproic acid intoxication in epileptology: diagnosis and treatment Abstract  similar documents
N. A. Shnaider, D. V. Dmitrenko
"... пациентов с генетически обусловленным замедлением метаболизма. Представлены современные методы клинической и ..."
Vol 11, No 3 (2019) Current views on neurosarcoidosis: pathogenesis, clinical manifestations, diagnosis Abstract  similar documents
M. S. Pushkaryov, L. M. Tibekina, L. P. Churilov
"... саркоидоз рассматривается как генетически детерминированное, полиэтиологическое и мультисистемное ..."
Vol 10, No 4 (2018) Pharmacogenetics of schizophrenia in real clinical practice: a clinical case Abstract  similar documents
R. F. Nasyrova, N. A. Schnaider, K. O. Mironov, G. A. Shipulin, O. P. Dribnokhodova, E. A. Golosov, M. Yu. Tolmachev, B. V. Andreev, A. A. Kurylev, L. Sh. Akhmetova, О. V. Limankin, N. G. Neznanov
"... антипсихотиков вариабельны и зависят от особенностей генетически детерминированных механизмов (транспортировки ..."
Vol 3, No 4 (2011) Current therapy for cognitive impairments Abstract  similar documents
N. V. Vakhnina
"... генетической предрасположенностью. Фармакотерапия легких и умеренных КР обычно включает вазоактивные ..."
Vol 6, No 3 (2014) Cognitive impairments in clinical practice and analyzing the work of a memory room in Yaroslavl (an outpatient reception) Abstract  similar documents
N. V. Pizova, M. V. Danilova
"... Genetics with Course of Neurosurgery, Yaroslavl State Medical Academy. The main goals of this subdivision ..."
Vol 10, No 3 (2018) MicroRNA expression profile in patients in the early stages of ischemic stroke Abstract  similar documents
I. S. Zhanin, V. A. Gusar, A. T. Timofeeva, V. G. Pinelis, A. Yu. Asanov
"... multifactorial nature and develops through the interaction of environmental factors and genetic predisposition ..."
Vol 6, No 3 (2014) Poststroke neuroplasticity processes Abstract  similar documents
I. V. Damulin, E. V. Ekusheva
"... наличии субкортикальных и корковых очагов. Подчеркивается, что имеются генетически детерминированные ..."
Vol 9, No 4 (2017) Membrane characteristics and vascular cognitive impairment Abstract  PDF (Eng)  similar documents
Yu. V. Zhitkova, D. R. Khasanova, V. N. Oslopov
"... ионотранспорта, отражающего генетически  детерминированные свойства клеточных мембран и определяемого методом ..."
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
"... BDNF с развитием височной эпилепсии. Пациенты и методы: проведено молекулярно-генетическое ..."
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