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Neurology, Neuropsychiatry, Psychosomatics

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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 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
"... of monogenic epilepsies in children are described; clinical and research justification of molecular-genetic ..."
 
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
 
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 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 10, No 2 (2018) Molecular mechanisms of action of glucosamine sulfate in the treatment of degenerative-dystrophic diseases of the joints and spine: results of proteomic analysis Abstract  similar documents
O. A. Gromova, I. Yu. Torshin, A. M. Lila, A. N. Gromov
"... Objective: to carry out a systems analysis of the molecular mechanisms of action ..."
 
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 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
"... to the development of four major phenotypes of OSAHS. It characterizes two basic approaches to a molecular genetic ..."
 
Vol 10, No 2 (2018) Diagnostic criteria for transient ischemic attack Abstract  similar documents
E. R. Lebedeva, N. M. Gurary, J. Olesen
"... to improve the diagnosis of TIA. It is recommended that the testing of these criteria in patients with TIA ..."
 
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
"... . The review considers the results of the most recent molecular pharmacological investigations ..."
 
Vol 9, No 3 (2017) Molecular effects of chondroguard in osteoarthritis and herniated discs Abstract  similar documents
A. M. Lila, O. A. Gromova, I. Yu. Torshin, A. G. Nazarenko, A. Yu. Gogolev
"... the molecular-physiological mechanisms of action of CS in intervertebral disc extrusions and protrusions. ..."
 
Vol 5, No 3 (2013) Prevention of venous thromboembolic events in ischemic stroke Abstract  similar documents
Vladimir Anatolyevich Parfenov
"... , and therapeutic gymnastics. The use of unfractionated heparin (UFH) and low-molecular-weight heparins (LMWH ..."
 
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 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 3, No 2 (2011) Autonomic neuropathy in diabetes mellitus: Clinical manifestations, diagnosis and treatment Abstract  similar documents
A. N. Barinov, M. V. Novosadova
"... it possible to prolong life and to improve its quality. The quantitative autonomic testing procedure permits ..."
 
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 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
 
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