المؤلفون: Levchuk, L., Losenkov, I., Pozhidaev, I., Osmanova, D., Simutkin, G., Bokhan, N., Loonen, A., Ivanova, S.A.

المصدر: Levchuk , L , Losenkov , I , Pozhidaev , I , Osmanova , D , Simutkin , G , Bokhan , N , Loonen , A & Ivanova , S A 2019 , ' Genes of neurotrophic factors and responsiveness to antidepressive psychopharmacotherapy in patients with depressive disorders ' , European Neuropsychopharmacology , vol. 29 , no. Supplement 1 , pp. S341-S342 . https://doi.org/10.1016/j.euroneuro.2018.11.532Test

مصطلحات موضوعية: antidepressant agent, brain derived neurotrophic factor, endogenous compound, phosphotransferase, prolactin, adult, basic research, chi square test, clinical feature, Clinical Global Impression scale, conference abstract, controlled study, data analysis software, drug therapy, female, gene frequency, gene mutation, genetic association, genetic susceptibility, genotype, Hamilton Depression Rating Scale, human, ICD-10, major clinical study, major depression, male, psychopharmacotherapy, remission, serotoninergic system, treatment response

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/0fa9e425-801d-46de-a418-60c5004ba49eTest

الإتاحة: https://doi.org/10.1016/j.euroneuro.2018.11.532Test
https://hdl.handle.net/11370/0fa9e425-801d-46de-a418-60c5004ba49eTest
https://research.rug.nl/en/publications/0fa9e425-801d-46de-a418-60c5004ba49eTest
https://pure.rug.nl/ws/files/76676662/1_s2.0_S0924977X18313798_main.pdfTest

المؤلفون: Boiko, A.S., Pozhidaev, I., Semke, A., Wilffert, B., Ivanova, S.A., Loonen, A.J.M.

المصدر: Boiko , A S , Pozhidaev , I , Semke , A , Wilffert , B , Ivanova , S A & Loonen , A J M 2019 , ' Tardive dyskinesia in schizophrenia : Gene polymorphisms of muscarinic and adrenergic receptors ' , European Neuropsychopharmacology , vol. 29 , no. Suppl. 1 , pp. S117-S118 . https://doi.org/10.1016/j.euroneuro.2018.11.223Test

مصطلحات موضوعية: alpha 1A adrenergic receptor, atypical antipsychotic agent, endogenous compound, muscarinic M1 receptor, muscarinic M2 receptor, muscarinic M4 receptor, Abnormal Involuntary Movement Scale, adult, Brazil, conference abstract, controlled study, female, gene frequency, gene mutation, genetic association, genetic susceptibility, genotype, human, incidence, informed consent, major clinical study, male, polymerase chain reaction, protein function, psychosis, side effect, tardive dyskinesia

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/827d89d3-59db-465d-a469-243266357fd7Test

الإتاحة: https://doi.org/10.1016/j.euroneuro.2018.11.223Test
https://hdl.handle.net/11370/827d89d3-59db-465d-a469-243266357fd7Test
https://research.rug.nl/en/publications/827d89d3-59db-465d-a469-243266357fd7Test
https://pure.rug.nl/ws/files/76677710/1_s2.0_S0924977X18310708_main.pdfTest

المؤلفون: Pozhidaev, I., Osmanova, D., Fedorenko, O., Vyalova, N., Semke, A., Wilffert, B., Loonen, A., Ivanova (Svetlana Ivanova), S.A.

المصدر: Pozhidaev , I , Osmanova , D , Fedorenko , O , Vyalova , N , Semke , A , Wilffert , B , Loonen , A & Ivanova (Svetlana Ivanova) , S A 2019 , ' The study of dopamine receptor genes in patients with schizophrenia ' , European Neuropsychopharmacology , vol. 29 , no. Suppl. 1 , pp. S410-S411 . https://doi.org/10.1016/j.euroneuro.2018.11.624Test

مصطلحات موضوعية: dopamine 1 receptor, dopamine 2 receptor, dopamine 3 receptor, dopamine 4 receptor, drug metabolizing enzyme, endogenous compound, adult, aged, Brazil, clinical article, conference abstract, controlled study, data analysis software, ethics, female, gender, gene frequency, gene mutation, genetic analyzer, genetic association, genetic marker, genetic susceptibility, genotype, human, ICD-10, male, mental hospital, multicenter study, pharmacogenetics, pharmacokinetics

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/4d85c316-243c-40de-b0cd-1ef6c5315a6dTest

الإتاحة: https://doi.org/10.1016/j.euroneuro.2018.11.624Test
https://hdl.handle.net/11370/4d85c316-243c-40de-b0cd-1ef6c5315a6dTest
https://research.rug.nl/en/publications/4d85c316-243c-40de-b0cd-1ef6c5315a6dTest
https://pure.rug.nl/ws/files/76677510/1_s2.0_S0924977X18314718_main.pdfTest

المؤلفون: Toshchakova, V.A. (Valentina A.), Bakhtiari, Y. (Yalda), Kulikov, A.V. (Alexander V.), Gusev, S.I. (Sergey I.), Trofimova, M.V. (Marina V.), Fedorenko, O. (Olga), Mikhalitskaya, E.V. (Ekaterina V.), Popova, N.K. (Nina K.), Bokhan, N.A. (Nikolay A.), Hovens, J.E.J.M. (Hans), Loonen, A.J.M. (Anton), Wilffert, B. (Bob), Ivanova, S.A.

المصدر: Neuropsychobiology, pp. 200-210

مصطلحات موضوعية: 5-HT2C receptor, Aggression, Genotype, Prisoners, Serotonin transporter

وصف الملف: application/pdf

العلاقة: http://repub.eur.nl/pub/105678Test; urn:hdl:1765/105678

الإتاحة: https://doi.org/10.1159/000487484Test
http://repub.eur.nl/pub/105678Test

المؤلفون: Geers, L.M., Pozhidaev, I.V., Ivanova, S.A., Freidin, M.B., Cohen, D., Boiko, A.S., Osmanova, D.Z., Fedorenko, O.Y., Touw, D.J., Semke, A.V., Wilffert, B., Bokhan, N.A., Loonen, A.J.M.

المصدر: Geers , L M , Pozhidaev , I V , Ivanova , S A , Freidin , M B , Cohen , D , Boiko , A S , Osmanova , D Z , Fedorenko , O Y , Touw , D J , Semke , A V , Wilffert , B , Bokhan , N A & Loonen , A J M 2017 , ' Association between P-glycoprotein polymorphisms and antipsychotic drug-induced hyperprolactinemia ' , European Neuropsychopharmacology , vol. 27 , no. Supplement 4 , pp. S956 . https://doi.org/10.1016/S0924-977XTest(17)31689-9

مصطلحات موضوعية: amisulpride, dopamine 2 receptor, endogenous compound, multidrug resistance protein 1, paliperidone, prolactin, risperidone, sulpiride, adult, brain, concentration ratio, DNA polymorphism, drug toxicity, enzyme linked immunosorbent assay, female, gene frequency, gene mutation, genetic model, genotype, human, human cell, hyperprolactinemia, major clinical study, male, membrane, parkinsonism, prevalence, prolactin blood level, prolactin secreting cell, psychosis

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/3bb53218-46ee-470d-84b8-3e5b09ff5825Test

الإتاحة: https://doi.org/10.1016/S0924-977XTest(17)31689-9
https://hdl.handle.net/11370/3bb53218-46ee-470d-84b8-3e5b09ff5825Test
https://research.rug.nl/en/publications/3bb53218-46ee-470d-84b8-3e5b09ff5825Test
https://pure.rug.nl/ws/files/50464636/1_s2.0_S0924977X17316899_main.pdfTest

المؤلفون: Pozhidaev, I., Alifirova, V.M., Freidin, M.B., Zhukova, I.A., Fedorenko, O.Y., Osmanova, D.Z., Mironova, Y.S., Wilffert, B., Ivanova, S.A., Loonen, A.J.M.

المصدر: Pozhidaev , I , Alifirova , V M , Freidin , M B , Zhukova , I A , Fedorenko , O Y , Osmanova , D Z , Mironova , Y S , Wilffert , B , Ivanova , S A & Loonen , A J M 2017 , ' Dopamine receptors genes polymorphisms in Parkinson patients with levodopa-induced dyskinesia ' , European Neuropsychopharmacology , vol. 27 , no. Supplement 4 , pp. S590 . https://doi.org/10.1016/S0924-977XTest(17)31129-X

مصطلحات موضوعية: biological marker, dopamine 2 receptor, dopamine 3 receptor, dopamine 4 receptor, endogenous compound, levodopa, phosphodiesterase I, Abnormal Involuntary Movement Scale, adult, adverse event, analyzer, cohort analysis, data analysis software, DNA extraction, drug metabolism, drug therapy, female, gender, gene frequency, gene mutation, genetic marker, genetic susceptibility, genotype, human, levodopa-induced dyskinesia, major clinical study, male, onset age, oxidative stress, Parkinson disease

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/49c63eae-168b-434c-a8e6-8245566e6df3Test

الإتاحة: https://doi.org/10.1016/S0924-977XTest(17)31129-X
https://hdl.handle.net/11370/49c63eae-168b-434c-a8e6-8245566e6df3Test
https://research.rug.nl/en/publications/49c63eae-168b-434c-a8e6-8245566e6df3Test
https://pure.rug.nl/ws/files/50464436/1_s2.0_S0924977X1731129X_main.pdfTest

المؤلفون: Fedorenko, O.Y., Ivanova, S.A., Loonen, A.J.M.

المساهمون: PharmacoTherapy, -Epidemiology and -Economics, Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET)

المصدر: European Neuropsychopharmacology, 26, S495-S496. ELSEVIER SCIENCE BV

مصطلحات موضوعية: n methyl dextro aspartic acid receptor 2B, n methyl dextro aspartic acid receptor 2A, side effect, endogenous compound, genotype, adverse drug reaction, interneuron, gene frequency, brain cortex, Russian (citizen), serotonin 2A receptor, mesencephalon, single nucleotide polymorphism, physical disability, thinking, dopamine 4 receptor, gene mutation, human, psychosis, dopaminergic activity, DNA extraction, Abnormal Involuntary Movement Scale, calculation, serotonin 2C receptor, dopamine 2 receptor, dopamine 3 receptor, tardive dyskinesia, atypical antipsychotic agent, dopamine release, dopamine, neurotransmitter, basal ganglion, genetic susceptibility, meta analysis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=narcis______::ab69f9915987423427cc7e45c33fe839Test
https://research.rug.nl/en/publications/0d73f041-f6d7-4ccf-88f0-c331012f8b47Test

المؤلفون: Boiko, A.S., Osmanova, D., Pozhidaev, I., Fedorenko, O., Ivanova, S.A., Semke, A., Bokhan, N., Loonen, A.J.M.

المصدر: Boiko , A S , Osmanova , D , Pozhidaev , I , Fedorenko , O , Ivanova , S A , Semke , A , Bokhan , N & Loonen , A J M 2016 , ' Gene polymorphism of neurotransmitter transporters in schizophrenic patients with drug-induced hyperprolactinemia ' , European Neuropsychopharmacology , vol. 26 , no. Supplement 2 , pp. S510-S511 . https://doi.org/10.1016/S0924-977XTest(16)31534-6

مصطلحات موضوعية: dopamine, dopamine transporter, endogenous compound, neuroleptic agent, neurotransmitter transporter, noradrenalin, noradrenalin transporter, prolactin, serotonin, vesicular monoamine transporter, adult, adverse drug reaction, analyzer, chi square test, controlled study, data analysis software, diagnosis, drug therapy, enzyme linked immunosorbent assay, female, gender, gene expression, gene frequency, gene mutation, genetic marker, genetic susceptibility, genotype, human, hyperprolactinemia, major clinical study

العلاقة: https://research.rug.nl/en/publications/4b515061-4e48-4733-a877-1ffe58b7d38bTest

الإتاحة: https://doi.org/10.1016/S0924-977XTest(16)31534-6
https://hdl.handle.net/11370/4b515061-4e48-4733-a877-1ffe58b7d38bTest
https://research.rug.nl/en/publications/4b515061-4e48-4733-a877-1ffe58b7d38bTest

المؤلفون: Ivanova, S.A., Alifirova, V.M., Pozhidaev, I.V., Fedorenko, O.Y., Osmanova, D.Z., Tiguntsev, V.V., Bokhan, N.A., Zhukova, I.A., Wilffert, B., Loonen, A.J.M.

المصدر: Ivanova , S A , Alifirova , V M , Pozhidaev , I V , Fedorenko , O Y , Osmanova , D Z , Tiguntsev , V V , Bokhan , N A , Zhukova , I A , Wilffert , B & Loonen , A J M 2016 , ' CYP2D6 and catechol-O-methyltransferase gene polymorphisms in Parkinson patients with levodopa-induced dyskinesias ' , European Neuropsychopharmacology , vol. 26 , pp. S656-S657 .

مصطلحات موضوعية: antioxidant, catechol methyltransferase, cytochrome P450 2D6, dopamine, endogenous compound, levodopa, methionine, neurotransmitter, neurotransmitter receptor, phosphodiesterase I, Abnormal Involuntary Movement Scale, adverse drug reaction, clinical trial, codon, data analysis software, disease carrier, disease duration, DNA extraction, dopamine uptake, drug therapy, gene frequency, genetic susceptibility, genotype, human, levodopa-induced dyskinesia, major clinical study, missense mutation, monoamine metabolism, odds ratio, onset age

العلاقة: https://research.rug.nl/en/publications/014e8ece-6d80-4997-9468-60cc28f28dd2Test

الإتاحة: https://hdl.handle.net/11370/014e8ece-6d80-4997-9468-60cc28f28dd2Test
https://research.rug.nl/en/publications/014e8ece-6d80-4997-9468-60cc28f28dd2Test

المؤلفون: Ivanova, S.A., Alifirova, V.M., Fedorenko, O.Y., Freidin, M.B., Bokhan, N.A., Zhukova, I., Al Hadithy, A.F.Y., Brouwers, J.R.B.J., Wilffert, B., Loonen, A.J.M.

المصدر: Ivanova , S A , Alifirova , V M , Fedorenko , O Y , Freidin , M B , Bokhan , N A , Zhukova , I , Al Hadithy , A F Y , Brouwers , J R B J , Wilffert , B & Loonen , A J M 2015 , ' Polymorphisms of DRD2, DRD3, DRD4 and HTR2C genes in levodopa-induced dyskinesias in Parkinson's disease ' , European Neuropsychopharmacology , vol. 25 , no. Supplement 2 , Abstract poster , pp. S589 . https://doi.org/10.1016/S0924-977XTest(15)30828-2

مصطلحات موضوعية: levodopa, serotonin receptor, neurotransmitter receptor, DOPA, dopamine, enzyme, dopamine receptor, n methyl dextro aspartic acid receptor, antioxidant, protein, phosphodiesterase I, DNA, n methyl dextro aspartic acid, levodopa-induced dyskinesia, gene, college, psychopharmacology, European, Parkinson disease, human, dyskinesia, limb, patient, phenotype, genotype, risk, drug metabolism, single nucleotide polymorphism, Abnormal Involuntary Movement Scale, receptor gene

العلاقة: https://research.rug.nl/en/publications/923bb3a0-8365-4859-9f95-d460994d28cbTest

الإتاحة: https://doi.org/10.1016/S0924-977XTest(15)30828-2
https://hdl.handle.net/11370/923bb3a0-8365-4859-9f95-d460994d28cbTest
https://research.rug.nl/en/publications/923bb3a0-8365-4859-9f95-d460994d28cbTest