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| Issue | Title | |
| Vol 16 (2024): (Suppl. 2) | Global transcriptome profiling of blood mononuclear cells from individuals with radiologically isolated syndrome reveals abnormalities characteristic of the rapid manifestation of multiple sclerosis symptoms | Abstract similar documents |
| M. S. Kozin, A. R. Kabaeva, M. A. Omarova, A. N. Boyko, O. O. Favorova, O. G. Kulakova | ||
| "... was performed using RNA sequencing on an MGISEQ-200 platform. Differential gene expression analysis ..." | ||
| Vol 14, No 1S (2022): Спецвыпуск: рассеянный склероз | Reduced expression of the tumor necrosis factor gene in blood mononuclear cells in radiologically isolated syndrome – validation of transcriptome analysis results | Abstract similar documents |
| M. S. Kozin, N. M. Baulina, I. S. Kiselev, A. R. Kabaeva, A. N. Boyko, O. O. Favorova, O. G. Kulakova | ||
| "... differences in the expression profiles of several genes in peripheral blood mononuclear cells (MNCs ..." | ||
| Vol 9, No 3 (2017) | Dandy–Walker malformation is a rare cause of syringomyelia in adults | Abstract similar documents |
| G. Yu. Evzikov, M. G. Bashlachev, K. A. Belozerskikh, V. A. Parfenov | ||
| "... раннем младенческом возрасте. Представлено наблюдение поздней клинической манифестации АДУ, которая стала ..." | ||
| Vol 12, No 1S (2020): Спецвыпуск: рассеянный склероз | Age at onset in multiple sclerosis as a possible predictor for cognitive impairment in children and adolescents | Abstract similar documents |
| M. D. Bogdanova, T. T. Batysheva, Yu. V. Mikadze, R. Ts. Bembeeva, E. Yu. Volkova | ||
| "... недостаточность различных сфер речевой деятельности. Возраст манифестации, продолжительность и частота рецидивов ..." | ||
| Vol 17, No 2 (2025) | Differences in cerebrospinal fluid microRNA profiles in patients with remitting multiple sclerosis and patients with other neurological diseases | Abstract similar documents |
| М. А. Omarova, М. S. Kozin, А. N. Boyko | ||
| "... of interactions with their target genes was created using the miRNet web service. Common targets were identified ..." | ||
| 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 | ||
| "... role in the modulation of nociception. The PRDM12 gene associated with congenital insensitivity to pain ..." | ||
| 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 | ||
| "... with episodic use of PAS depending on the rs10121864 genotype of the PRDM12 gene. Patients and methods ..." | ||
| 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 the polymorphic variants of glutamatergic system genes, such as GRIN2A encoding the N-methyl-D-aspartate (NMDA ..." | ||
| Vol 14, No 1S (2022): Спецвыпуск: рассеянный склероз | Free circulating miRNA as a potential diagnostic marker in multiple sclerosis (review) | Abstract similar documents |
| M. A. Omarova, M. S. Kozin, A. N. Boyko | ||
| "... of the expression of protein coding genes, are known to be present in CSF and can be considered as potential markers ..." | ||
| 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 | ||
| "... Objective: to study the association of the DRD4, DAT genes with vital exhaustion in an open 25—64 ..." | ||
| 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 | ||
| "... rs2278749 of the ARNTL gene among individuals aged 25–64 years living in Novosibirsk. Material ..." | ||
| 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 13, No 2 (2021) | Adult metachromatic leukodystrophy: case report | Abstract similar documents |
| T. I. Prusova, P. A. Reznichenko, K. D. Yakovleva, D. V. Dmitrenko | ||
| "... ARSA gene mutations. Clinical and genetic characteristics of the adult MLD and modern treatment ..." | ||
| Vol 14, No 6 (2022) | Leptomeningeal amyloidosis: features of the clinical picture (clinical observation) | Abstract similar documents |
| E. I. Safiulina, O. E. Zinovieva, N. S. Shcheglova, V. V. Rameev, Z. V. Surnina, E. N. Nikitina, O. A. Vorobieva | ||
| "... gene mutation. The leptomeningeal form is a rare phenotypic variant of amyloidosis with a predominant ..." | ||
| Vol 13, No 6 (2021) | Efficacy and safety of anti-CGRP(r) monoclonal antibodies in real clinical practice: preliminary analysis after three months of therapy | Abstract similar documents |
| N. V. Vashchenko, D. Z. Korobkova, K. V. Skorobogatykh, Yu. E. Azimova | ||
| "... Monoclonal antibodies inhibiting calcitonin gene related peptide (CGRP) or its receptor have been ..." | ||
| 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 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 14, No 5 (2022) | Application of a new biological pathogenetic therapy of migraine in clinical practice: expert consensus of the Russian Headache Research Society | Abstract similar documents |
| A. V. Sergeev, G. R. Tabeeva, E. G. Filatova, A. V. Amelin, L. R. Akhmadeeva, E. R. Lebedeva, V. V. Osipova, Yu. E. Azimova, N. V. Latysheva, O. B. Doronina, K. V. Skorobogatykh | ||
| "... ) to the calcitonin gene related peptide (CGRP) ligand or receptor. These recommendations are based on current ..." | ||
| 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 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 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 ..." | ||
| 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 ..." | ||
| 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 | ||
| "... 6265 in BDNF gene. Research groups have shown increased expression of BDNF in the hippocampus ..." | ||
| 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 | ||
| "... occurrence is associated with polymorphic allelic variants in BRD2 gene (locus EJM3) and GJD2 gene (locus EJM ..." | ||
| 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 | ||
| "... –Sträussler–Scheinker syndrome with a verified p.P102L mutation in the PRNP gene. The clinical picture ..." | ||
| 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 | ||
| "... nucleotide variants of genes (SNGs) encoding proteins of neuroinflammation and neurodegeneration ..." | ||
| 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 | ||
| "... gene and sleep disorders in the open population of the able-bodied population aged 25–44 years ..." | ||
| Vol 12, No 4 (2020) | Current concept of the pathophysiology of migraine and new targets for its therapy | Abstract PDF (Eng) similar documents |
| G. R. Tabeeva, Z. Katsapava | ||
| 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 | ||
| "... -methyl transferase (COMT) gene with vital exhaustion (VE) in a 45–64-year-old population. Patients ..." | ||
| 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 16, No 1 (2024) | Safety and efficacy of fremanezumab in real clinical practice in patients with chronic migraine | Abstract similar documents |
| G. N. Belskaya, A. V. Krasnikov, E. A. Kiryanova, M. E. Prokopovich, E. V. Sakharova, G. V. Makarov | ||
| Vol 16, No 4 (2024) | Gerstmann–Sträussler–Scheinker syndrome with phenotypic change in dynamics and misdiagnosis of a motor neurone disease (clinical case) | Abstract similar documents |
| D. V. Shevchuk, D. A. Grishina, E. P. Nuzhny, M. N. Zakharova | ||
| "... in the prion protein gene PRNP was identified. It is discussed whether GSS should be included ..." | ||
| 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 | ||
| "... likely to carry the minor allele C of the 1298A>C polymorphism of the MTHFR gene and the minor allele G ..." | ||
| 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 | ||
| "... , the polymorphic variants in the ABCB1 gene may affect the safety of this drug. Objective: to analyze ..." | ||
| 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 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 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 | ||
| "... of CLOCK gene activity with both affective disorders and alcohol use/dependence disorders; in particular ..." | ||
| Vol 15, No 2 (2023) | Rapidly progressive dementia with early onset associated with the I143T mutation in the PSEN1 gene: a clinical case in a family from Russia | Abstract similar documents |
| Yu. A. Shpilyukova, A. O. Protopopova, N. Yu. Abramycheva, E. Yu. Fedotova, S. N. Illarioshkin | ||
| "... with a verified Ile143Thr mutation in the PSEN1 gene in a Russian family with a phenotype similar ..." | ||
| 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 | ||
| Vol 16, No 6 (2024) | Evaluation of the content of microbial metabolites in cerebrospinal fluid of individuals with radiologically isolated syndrome | Abstract similar documents |
| M. A. Omarova, O. G. Zhilenkova, A. N. Boyko | ||
| "... состояние – радиологически изолированный синдром (РИС), изучению микробиома при котором уделено меньше ..." | ||
| 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 | ||
| "... and depression. The authors of relevant publications indicate associations between polymorphic melatonin genes ..." | ||
| 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 | ||
| "... -methyl transferase (COMT) gene with depression in an open population aged 25–44 years. Patients ..." | ||
| 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 13, No 1S (2021): Спецвыпуск: рассеянный склероз | Microbiota markers level in the cerebrospinal fluid of patients with multiple sclerosis and radiologically isolated syndrome | Abstract similar documents |
| A. N. Boyko, M. V. Melnikov, O. V. Boyko, A. R. Kabaeva, M. A. Omarova, O. G. Zhilenkova, A. M. Zatevalov, V. S. Rogovskii | ||
| "... микробных маркеров в ЦСЖ пациентов с РС и радиологически изолированным синдромом (РИС). Пациенты и методы ..." | ||
| Vol 13, No 1S (2021): Спецвыпуск: рассеянный склероз | Clinical and epidemiological characteristics of multiple sclerosis in students in the Republic of Bashkortostan | Abstract similar documents |
| A. V. Tukhvatullin, U. Sh. Kuzmina, N. F. Utyagulova, R. F. Talisov, V. A. Vakhitov, K. Z. Bakhtiyarova | ||
| "... В последние годы фиксируется расширение возрастного диапазона манифестации рассеянного склероза ..." | ||
| Vol 13, No 1 (2021) | Pediatric migraine equivalents | Abstract similar documents |
| P. V. Zhmylyova, G. R. Tabeeva, A. V. Sergeev | ||
| "... тесно связаны с мигренью и чаще наблюдаются у детей задолго до манифестации мигренозной головной боли. В ..." | ||
| 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 | ||
| "... оказывать взаимное влияние на клиническую манифестацию, тяжесть и темпы прогрессирования КН. Болезнь ..." | ||
| Vol 5, No 3 (2013) | Comorbidity of chronic pain and depression in neurological patients | Abstract similar documents |
| Gyuzel Rafkatovna Tabeeva | ||
| "... . Хроническая боль и депрессия оказывают взаимное влияние на клиническую манифестацию, течение и эффективность ..." | ||
| Vol 12, No 5 (2020) | Chemotranscriptome analysis of the ethylmethylhydroxypyridine succinate molecule in the context of postgenomic pharmacology | Abstract similar documents |
| O. A. Gromova, I. Yu. Torshin, A. I. Sorokin, V. A. Semenov, L. V. Stakhovskaya | ||
| "... effects of EMHPS on the transcription of 12,700 annotated human genes in the neural progenitor cells (NPC ..." | ||
| 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 | ||
| "... locus) genes has been established. Objective: to establish risk factors for JME in terms of a genetic ..." | ||
| 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 12, No 4 (2020) | Chemotranscriptome analysis indicates the neurotrophic and neuromodulator effects of a citicoline molecule | Abstract similar documents |
| I. Yu. Torshin, O. A. Gromova, L. V. Stakhovskaya, V. A. Semenov, I. A. Shchukin | ||
| "... Objective: to investigate the effect of citicoline (CTC) on gene transcription. Material ..." | ||
| Vol 12, No 6 (2020) | COVID-19 and mental health: challenges and first conclusions | Abstract similar documents |
| V. E. Medvedev, O. A. Dogotar | ||
| "... . Манифестация или обострение психических заболеваний в свою очередь способствуют распространению вирусной ..." | ||
| 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 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 14, No 2 (2022) | Changes in expression of miRNAs from the DLK1-DIO3 locus are characteristic of relapsing-remitting multiple sclerosis regardless of the disease activity | Abstract similar documents |
| N. M. Baulina, A. R. Kabaeva, A. N. Boyko, O. O. Favorova | ||
| "... in the expression of 26 microRNA genes localized in the DLK1-DIO3 locus in men with relapsing-remitting MS (RRMS ..." | ||
| 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 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 7, No 1 (2015) | Stress-related cognitive and non-cognitive impairments in elderly patients | Abstract similar documents |
| G. R. Tabeeva | ||
| "... Старение – это физиологический процесс, который может длительно развиваться без манифестации ..." | ||
| Online-first | ИНСОМНИЯ У ПАЦИЕНТОВ С МИГРЕНЬЮ | Abstract similar documents |
| , | ||
| "... проявляется перекрытием клинической манифестации, но также в значительной степени предопределяет их ..." | ||
| Vol 12, No 2 (2020) | Neurocutaneous melanosis concurrent with a posterior cranial fossa cyst (Dandy–Walker complex) and an intradural arachnoid cyst of the spinal canal | Abstract similar documents |
| G. Yu. Evzikov, M. G. Bashlachev, E. V. Shashkova, K. A. Belozerskikh, F. V. Grebenev | ||
| "... интерес то, что манифестация неврологических симптомов и верификация диагноза произошли уже во взрослом ..." | ||
| Vol 11, No 2 (2019) | Insomnia in patients with migraine | Abstract similar documents |
| E. M. Evdokimova, G. R. Tabeeva | ||
| "... проявляется «перекрытием» клинической манифестации, но и в значительной степени предопределяет их естественное ..." | ||
| Vol 8, No 2 (2016) | Alzheimer's disease under the mask of stroke | Abstract similar documents |
| A. A. Naumenko, N. V. Vakhnina | ||
| "... нейродегенеративный процесс, чаще всего – болезнь Альцгеймера (БА). Инсульт может способствовать манифестации ..." | ||
| Vol 10, No 2 (2018) | The relationship and interaction of menstrual and generative function and depressive disorders in women | Abstract PDF (Eng) similar documents |
| N. A. Tyuvina, E. O. Voronina, V. V. Balabanova, E. M. Goncharova | ||
| "... адаптация страдают у женщин с манифестацией депрессии в постменопаузе. Заключение. Начало депрессивных ..." | ||
| Vol 6, No 3 (2014) | Psychogenic urticaria: The issues of diagnosis and optimization of therapy | Abstract similar documents |
| A. A. Pribytkov, E. A. Orlova | ||
| "... : наличие психотравмирующей ситуации, манифестация кожных проявлений после психогении, высокий уровень ..." | ||
| 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 16, No 2 (2024) | Refractory migraine | Abstract similar documents |
| G. R. Tabeeva, O. V. Kosivtsova, N. A. Kovalchuk, T. A. Orlyuk | ||
| "... . Currently, the use of monoclonal antibodies against calcitonin gene-related peptide is the best-studied ..." | ||
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| "... II, molecular genetic research of SNVs rs1800497 of DRD2 gene (DRD2/ANKK1 Taq1A), rs4680 of COMT gene ..." | ||
| Vol 14, No 2 (2022) | Clinical features of atypical depression in bipolar and recurrent affective disorders, psychogenic depression | Abstract PDF (Eng) similar documents |
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