Zobrazeno 1 - 10
of 166
pro vyhledávání: '"R, Ebstein"'
Autor:
J Granich, C Dalman, M Rayar, A Weitlauf, L H Pedersen, N Yirmiya, V Gluncic, L M Elder, K M Abel, M Dubray, L Hoglund Carlsson, D Spiegelman, S L Buka, T Hashimoto, S Saltvedt, B M Anderlid, C J Williams, C Wang, H Geng, R Ebstein, M R Torloni, K Hobbs, H Ito, S J Webb, C Rodgers, B M Kuehn, L K Curran, M Hickey, A Fukumoto, M F Blaxill, E S Ang, Y K Stoch, W Liu, A Duque, J S Abramowicz, H Gardener, A J Whitehouse, C J Newschaffer, F J Stanley, A C Svensson, M L McPheeters, C B Miltoft, M Gamliel, A Kennedy, A M McClintic, S G Hellmuth, A Vehorn, N Vedmedovska, M Merialdi, N Bashir, B H King, M Penner, K Toth, G Dawson
Publikováno v:
Ultraschall in der Medizin - European Journal of Ultrasound. 38:452-453
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edf75125c66a9bd15cd0108c01a43862
https://doi.org/10.1055/s-0043-116425
https://doi.org/10.1055/s-0043-116425
Autor:
K, Brookes, X, Xu, W, Chen, K, Zhou, B, Neale, N, Lowe, R, Anney, R, Aneey, B, Franke, M, Gill, R, Ebstein, J, Buitelaar, P, Sham, D, Campbell, J, Knight, P, Andreou, M, Altink, R, Arnold, F, Boer, C, Buschgens, L, Butler, H, Christiansen, L, Feldman, K, Fleischman, E, Fliers, R, Howe-Forbes, A, Goldfarb, A, Heise, I, Gabriëls, I, Korn-Lubetzki, L, Johansson, R, Marco, S, Medad, R, Minderaa, F, Mulas, U, Müller, A, Mulligan, K, Rabin, N, Rommelse, V, Sethna, J, Sorohan, H, Uebel, L, Psychogiou, A, Weeks, R, Barrett, I, Craig, T, Banaschewski, E, Sonuga-Barke, J, Eisenberg, J, Kuntsi, I, Manor, P, McGuffin, A, Miranda, R D, Oades, R, Plomin, H, Roeyers, A, Rothenberger, J, Sergeant, H-C, Steinhausen, E, Taylor, M, Thompson, S V, Faraone, P, Asherson
Publikováno v:
Molecular Psychiatry, 11(6), 934-953. Nature Publishing Group
Molecular Psychiatry, 11, 934-953. Nature Publishing Group
Molecular Psychiatry, 11, 10, pp. 934-53
Molecular Psychiatry, 11, 934-53
Molecular psychiatry, 11(10), 934-953. Nature Publishing Group
Brookes, K, Xu, X, Chen, W, Zhou, K, Neale, B, Lowe, N, Aneey, R, Franke, B, Gill, M, Ebstein, R, Buitelaar, J, Sham, P, Campbell, D, Knight, J, Andreou, P, Altink, M, Arnold, R, de Boer, F, Buschgens, C, Butler, L, Christiansen, H, Feldman, L, Fleischman, K, Fliers, E, Howe-Forbes, R, Goldfarb, A, Heise, A, Gabriels, I, Korn-Lubetzki, I, Marco, R, Medad, S, Minderaa, R, Mulas, F, Muller, U, Mulligan, A, Rabin, K, Rommelse, N N J, Sethna, V, Sorohan, J, Uebel, H, Psychogiou, L, Weeks, A, Barrett, R, Craig, I, Banaschewski, T, Sonuga-Barke, E, Eisenberg, J, Kuntsi, J, Manor, I, McGuffin, P, Miranda, A, Oades, R D, Plomin, R, Roeyers, H, Rothenberger, A, Sergeant, J A, Steinhausen, H C, Taylor, E, Thompson, M, Faraone, S V, Asherson, P & Johansson, L 2006, ' The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes ', Molecular Psychiatry, vol. 11, no. 6, pp. 934-953 . https://doi.org/10.1038/sj.mp.4001869
Molecular Psychiatry, 11, 934-953. Nature Publishing Group
Molecular Psychiatry, 11, 10, pp. 934-53
Molecular Psychiatry, 11, 934-53
Molecular psychiatry, 11(10), 934-953. Nature Publishing Group
Brookes, K, Xu, X, Chen, W, Zhou, K, Neale, B, Lowe, N, Aneey, R, Franke, B, Gill, M, Ebstein, R, Buitelaar, J, Sham, P, Campbell, D, Knight, J, Andreou, P, Altink, M, Arnold, R, de Boer, F, Buschgens, C, Butler, L, Christiansen, H, Feldman, L, Fleischman, K, Fliers, E, Howe-Forbes, R, Goldfarb, A, Heise, A, Gabriels, I, Korn-Lubetzki, I, Marco, R, Medad, S, Minderaa, R, Mulas, F, Muller, U, Mulligan, A, Rabin, K, Rommelse, N N J, Sethna, V, Sorohan, J, Uebel, H, Psychogiou, L, Weeks, A, Barrett, R, Craig, I, Banaschewski, T, Sonuga-Barke, E, Eisenberg, J, Kuntsi, J, Manor, I, McGuffin, P, Miranda, A, Oades, R D, Plomin, R, Roeyers, H, Rothenberger, A, Sergeant, J A, Steinhausen, H C, Taylor, E, Thompson, M, Faraone, S V, Asherson, P & Johansson, L 2006, ' The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes ', Molecular Psychiatry, vol. 11, no. 6, pp. 934-953 . https://doi.org/10.1038/sj.mp.4001869
Contains fulltext : 35205.pdf (Publisher’s version ) (Closed access) Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, starting in early childhood and persisting into adulthood in the majority of cases. Family
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c1aaf3948cbed1dfbee5b0acf57d54f
https://hdl.handle.net/2066/35205
https://hdl.handle.net/2066/35205
Akademický článek
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Publikováno v:
Bulletin of experimental biology and medicine. 145(1)
We studied the relationship between DRD5 gene polymorphism presented by microsatellites with cognitive signs in 152 schizophrenic patients, 81 mentally healthy relatives, and 125 mentally healthy control individuals. An association was found between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b5fdef30ca3703934a1ea5a24785a40
https://pubmed.ncbi.nlm.nih.gov/19024005
https://pubmed.ncbi.nlm.nih.gov/19024005
Autor:
X, Xu, E A, Duman, E, Aysimi, R, Anney, K, Brookes, B, Franke, K, Zhou, C, Buschgens, W, Chen, H, Christiansen, J, Eisenberg, I, Gabriëls, I, Manor, R, Marco, U C, Müller, A, Mulligan, N, Rommelse, M, Thompson, H, Uebel, T, Banaschewski, J, Buitelaar, R, Ebstein, M, Gill, A, Miranda, F, Mulas, R D, Oades, H, Roeyers, A, Rothenberger, J, Sergeant, E, Sonuga-Barke, H-C, Steinhausen, E, Taylor, S V, Faraone, P, Asherson
Publikováno v:
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 7, pp. 1306-9
Xu, X, Aysimi, E, Anney, R J, Brookes, K, Franke, B, Zhou, K, Buschgens, C J M, Chen, W, Christiansen, H, Eisenberg, J, Gabriëls, I, Manor, I, Marco, R, Müller, U, Mulligan, A, Rommelse, N N J, Thompson, M, Uebel, H, Banaschewski, T, Buitelaar, J K, Ebstein, R, Gill, M, Miranda, A, Mulas, F, Oades, R D, Roeyers, H, Rothenberger, A, Sergeant, J A, Sonuga-Barke, E, Steinhausen, H C, Taylor, E, Faraone, S V & Asherson, P 2008, ' No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 7, pp. 1306-1309 . https://doi.org/10.1002/ajmg.b.30737
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(7), 1306-1309. Wiley-Liss Inc.
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1306-9
Xu, X, Aysimi, E, Anney, R J, Brookes, K, Franke, B, Zhou, K, Buschgens, C J M, Chen, W, Christiansen, H, Eisenberg, J, Gabriëls, I, Manor, I, Marco, R, Müller, U, Mulligan, A, Rommelse, N N J, Thompson, M, Uebel, H, Banaschewski, T, Buitelaar, J K, Ebstein, R, Gill, M, Miranda, A, Mulas, F, Oades, R D, Roeyers, H, Rothenberger, A, Sergeant, J A, Sonuga-Barke, E, Steinhausen, H C, Taylor, E, Faraone, S V & Asherson, P 2008, ' No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 147B, no. 7, pp. 1306-1309 . https://doi.org/10.1002/ajmg.b.30737
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B(7), 1306-1309. Wiley-Liss Inc.
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 147B, 1306-9
Contains fulltext : 71091.pdf (Publisher’s version ) (Closed access) Several independent studies have reported association between serotonin transporter gene (SLC6A4) polymorphisms and attention deficit hyperactivity disorder (ADHD). Five studies f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddf99ffc23244fcc384d44f4aae6d721
https://hdl.handle.net/2066/71091
https://hdl.handle.net/2066/71091
Autor:
M V, Alfimova, V E, Golimbet, I K, Gritsenko, T V, Lezheĭko, L I, Abramova, M A, Strel'tsova, I V, Khlopina, R, Ebstein
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 106(7)
To elucidate main effects of dopamine receptor D4 (DRD4) and cathecol-O-methyltransferase (COMT) genes as well as their interaction effect on neurocognitive traits, DRD4 gene polymorphisms (-809G/A, -521C/T) and the COMT gene Val158Met polymorphism,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd1b915a458a3cd93d4e155a6d59a56c
https://pubmed.ncbi.nlm.nih.gov/16921721
https://pubmed.ncbi.nlm.nih.gov/16921721
Autor:
I, Manor, R, Ebstein
Publikováno v:
Harefuah. 139(9-10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::30014009abe8b0d5c85c8812c18332d3
https://pubmed.ncbi.nlm.nih.gov/11341221
https://pubmed.ncbi.nlm.nih.gov/11341221
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
M. Alfimova, V. Golimbet, I. Gritsenko, T. Lezheiko, L. Abramova, M. Strel’tsova, I. Khlopina, R. Ebstein
Publikováno v:
Neuroscience & Behavioral Physiology; Sep2007, Vol. 37 Issue 7, p643-650, 8p
Publikováno v:
Neuroscience & Behavioral Physiology; Jul2007, Vol. 37 Issue 6, p601-606, 6p