Preview

Neurology, Neuropsychiatry, Psychosomatics

Advanced search

Search


Order results by:     
 
Issue Title
 
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
"... phenotypes of OSAHS, in the development of which there may be a genetic component. It is stated that a study ..."
 
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 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 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
"... The paper describes a clinical case of idiopathic generalized epilepsy with a variable phenotype ..."
 
Vol 11, No 2S (2019): Спецвыпуск: боль в спине и конечностях A patient with osteoarthritis out of a doctor's field of vision: how should joint pain be controlled within the concept of responsible self-treatment? Abstract  similar documents
A. E. Karateev
"... of long-term prognosis. This is determined by the heterogeneity of OA, different phenotypes ..."
 
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 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 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 ..."
 
Vol 8, No 4 (2016) GENETIC AND FUNCTIONAL FACTORS IN THE DEVELOPMENT OF COGNITIVE IMPAIRMENT IN HYPERTENSION: A PROSPECTIVE STUDY Abstract  similar documents
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 ..."
 
Online-first Features of pathogenesis and clinical manifestation of Parkinson's disease developed from essential tremor Abstract  similar documents
A. V. Kudrevatykh, I. V. Miliukhina
 
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
"... слова: генетические эпилептические энцефалопатии у детей; эпилепсия; видео-электроэнцефалографический ..."
 
Vol 4, No 4 (2012) Sleep disorders in neurological practice Abstract  similar documents
Mikhail Guryevich Poluektov
"... обструктивного апноэ сна. Характерными неврологическими заболеваниями являются синдром беспокойных ног и ..."
 
Vol 4, No 1 (2012) Generalized epilepsies: current conceptions and therapeutic approaches Abstract  similar documents
L R Zenkov
"... genetic abnormality shows diverse focal and generalized phenotypes in different members of one family ..."
 
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
 
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 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
"... , Россия; 3ФГБНУ «Медико-генетический научный центр», лаборатория наследственных болезней обмена веществ ..."
 
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 ..."
 
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 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 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 1, No 1 (2009) CONCOMITANCE OF INFANTILE AUTISM AND EPILEPSY: ETIOPATHOGENIC ASPECTS Abstract  similar documents
E V Malinina, S A Suprun, E A Markova, 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 7, No 1 (2015) Obstructive sleep apnea syndrome as an accident risk factor in professional drivers in Yekaterinburg. Dangerous Sleep (DS-1) study Abstract  similar documents
A. A. Belkin, E. V. Alekseeva, O. V. Zhigulskaya, E. K. Romanova
"... апноэ сна (СОАС). Цель исследования – изучение соматического и психологического состояния, нарушений ..."
 
Vol 3, No 4 (2011) Mechanisms in the pathogenesis of poststroke spasticity Abstract  similar documents
Elina Anatolyevna Katushkina, O E Zinovyeva, B S Shenkman, N N Yakhno
"... exhibited myosin phenotype transformation with a preponderance of fast type II fibers ..."
 
Vol 9, No 4 (2017) Current approaches to diagnosing and treating major neurocognitive disorder Abstract  similar documents
A. A. Kulesh, V. V. Shestakov
"... reflects the  main clinical phenotype of AD. Magnetic resonance morphometry,  amyloid positron emission ..."
 
Vol 9, No 3 (2017) The severity of respiratory disorders in different forms of amyotrophic lateral sclerosis Abstract  similar documents
Yu. N. Rushkevich, N. M. Chechik, S. A. Likhachev, O. V. Merkul, T. V. Korbut
"... которых имелись достоверно более высокие показатели индекса апноэ/гипопноэ (ИАГ) и индекса десатурации (ИД ..."
 
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 10, No 4 (2018) Immunophenotypic characteristics of brain metastases Abstract  similar documents
G. A. Demyashkin, E. A. Shalamova, P. V. Nikitin, S. N. Bogomolov
"... to obtain the following tumor phenotypes in the patients: CK5/6+, p63+, CK7+, UPIII+ (urothelial cancer) (n ..."
 
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 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 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 9, No 1 (2017) The impact of sleep-disordered breathing on early functional recovery in ischemic stroke Abstract  similar documents
G. M. Lutokhin, L. A. Geraskina, A. V. Fonyakin, M. Yu. Maksimova
"... «ишемической полутени». Нарушения дыхания во сне (НДС) проявляются интермиттирующими эпизодами апноэ и гипопноэ ..."
 
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 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 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
"... некоторых за- болеваниях человека. В последние годы генетические ис- следования таких заболеваний и изучение ..."
 
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 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 ..."
 
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 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 ..."
 
Vol 4, No 2 (2012) Strokes in mitochondrial diseases Abstract  similar documents
N V Pizova
"... . Этот синдром является генетически детерминирован- ным и относится к группе митохондриальных болезней ..."
 
Vol 9, No 1S (2017): SPECIAL ISSUE: EPILEPSY Epidemiology of juvenile myoclonic epilepsy Abstract  similar documents
O. S. Shilkina, N. A. Schnaider
"... фенотипом, подразумевая, что ЮМЭ не существует в качестве единственного феноти- О Р И Г И Н А Л Ь Н Ы Е И ..."
 
Vol 3, No 3 (2011) Epilepsy and nicotine: Clinical observations and a review of literature  similar documents
L R Zenkov, A A Shatenshtein
"... эксайтонейротоксичности, пока- зана в экспериментах [31]. В основе ряда форм эпилепсии лежит генетически ..."
 
Vol 9, No 1 (2017) Some risk factors of stroke in dwellers of the Republic of Tyva Abstract  similar documents
B. M. Doronin, Kh. D. Mongush
"... , синдром апноэ во сне, мигрень с аурой [10, 11]. АГ – наиболее распространенный, общепризнанный и ..."
 
1 - 50 of 220 Items 1 2 3 4 5 > >> 

Search tips:

  • Search terms are case-insensitive
  • Common words are ignored
  • By default articles containing any term in the query are returned (i.e., OR is implied)
  • Make sure that a word exists in an article by prefixing it with +; e.g., +journal +access scholarly academic
  • Combine multiple words with AND to find articles containing all terms; e.g., education AND research
  • Exclude a word by prefixing it with - or NOT; e.g., online -politics or online NOT politics
  • Search for an exact phrase by putting it in quotes; e.g., "open access publishing". Hint: Quoting Chinese or Japanese words will help you to find exact word matches in mixed-language fields, e.g. "中国".
  • Use parentheses to create more complex queries; e.g., archive ((journal AND conference) NOT theses)