tallózása szerző szerint "Barta, Csaba"

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  • A komorbid figyelemhiányos/hiperaktivitás- és szerhasználati zavart mutató betegek szűrésére, diagnosztikájára és kezelésére vonatkozó ajánlások. [Recommendations for the screening, diagnosis and treatment of patients with comorbid attention deficit hyperactivity- and substance use disorder]. 
    Kapitány-Fövény, Máté; Barta, Csaba; Crunelle, Cleo L; van den Brink, Wim; Moggi, Franz; Konstenius, Maija; Franck, Johan; Levin, Frances R; van de Glind, Geurt; Coetzee, Corné; Luderer, Mathias; Schellekens, Arnt; Matthys, Frieda; Demetrovics, Zsolt; Akerele, Evaristo; Brynte, Christoffer; Dalsgaard, Soren; Dom, Geert; Faraone, Stephen; Kaye, Sharlene; Lim, Carol; Paraskevopoulou, Maria; Velez Pastrana, Maria; Richman, Mara; Seesink, Henk-Jan; Skutle, Arvid; van Emmerik-van Oortmerssen, Katelijne; van Kernebeek, Michiel; Verspeet, Sofie (2020)
    Among patients with substance use disorders (SUD), adult attention deficit hyperactivity disorder (ADHD) is one of the most frequently co-occuring disorder. Those SUD patients with comorbid ADHD show earlier onset of ...
  • Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort 
    Bertelsen B; Stefánsson H; Riff Jensen L; Melchior L; Mol Debes N; Groth C; Skov L; Werge T; Karagiannidis I; Tárnok, Zsanett; Barta, Csaba; Nagy, Péter; Farkas L; Brøndum-Nielsen K; Rizzo R; Gulisano M; Rujescu D; Kiemeney LA; Tosato S; Nawaz MS; Ingason A; Unnsteinsdottir U; Steinberg S; Ludvigsson P; Stefansson K; Kuss AW; Paschou P; Cath D; Hoekstra PJ; Müller-Vahl K; Stuhrmann M; Silahtaroglu A; Pfundt R; Tümer Z (2016)
    Background: Gilles de la Tourette syndrome (GTS) is a complex neuropsychiatric disorder with a strong genetic influence where copy number variations are suggested to play a role in disease pathogenesis. In a previous ...
  • Association of GDNF and CNTNAP2 gene variants with gambling 
    Das, Arundhuti; Pagliaroli, Luca; Vereczkei, Andrea; Kótyuk, Eszter; Langstieh, Banrida; Demetrovics, Zsolt; Barta, Csaba (2019)
    Some form of gambling can be observed in nearly every society, as the gratification felt upon winning in uncertain conditions is universal. A culturally distinct form of gambling, associated with a traditional sporting ...
  • Childhood trauma exposure in substance use disorder patients with and without ADHD 
    Konstenius M; Leifman A; van Emmerik-van Oortmerssen K; van de Glind G; Franck J; Moggi F; Ramos-Quiroga JA; Levin FR; Carpentier PJ; Skutle A; Bu E-T; Kaye S; Demetrovics, Zsolt; Barta, Csaba; Auriecomb M; Fatséas M; Johnson B; Faraone SV; Allsop S; Carruthers S; Schoevers RA; Verspreet S; Dom G; Koeter MWJ; van den Brink W (2017)
    Background Childhood trauma exposure (CTE) is frequently reported by those with substance use disorders (SUDs). SUDs also frequently co-occur with attention deficit hyperactivity disorder (ADHD). Objective To investigate ...
  • Co-occurrences of substance use and other potentially addictive behaviors 
    Kóyuk, Eszter; Magi, Anna Katalin; Eisinger, Andrea; Király, Orsolya; Vereczkei, Andrea; Barta, Csaba; Griffiths, Mark D; Székely, Anna; Kökönyei, Gyöngyi; Farkas, Judit; Kun, Bernadette; Badgaiyan, Rajendra D; Urbán, Róbert; Blum, Kenneth; Demetrovics, Zsolt (2020)
    Changes in the nomenclature of addictions suggest a significant shift in the conceptualization of addictions, where non-substance related behaviors can also be classified as addictions. A large amount of data provides ...
  • Early developmental, temperamental and educational problems in 'substance use disorder' patients with and without ADHD: Does ADHD make a difference? 
    Skutle, A; Bu, ETH; Jellestad, FK; van Emmerik-van Oortmerssen, K; Dom, G; Verspreet, S; Carpentier, PJ; Ramos-Quiroga, JA; Franck, J; Konstenius, M; Kaye, S; Demetrovics, Zsolt; Barta, Csaba; Fatséas, M; Auriacombe, M; Johnson, B; Faraone, SV; Levin, FR; Allsop, S; Carruthers, S; Schoevers, RA; Koeter, MWJ; van den Brink, W; Moggi, F; Møller, M; van de Glind, G (2015)
  • Epigenome-Wide Association Study of Tic Disorders 
    Zilhão NR; Padmanabhuni SS; Pagliaroli, Luca; Barta, Csaba; BIOS Consortium; Smit DJA; Cath D; Nivard MG; Baselmans BML; Van Dongen J; Paschou P; Boomsma DI (2015)
    Tic disorders are moderately heritable common psychiatric disorders that can be highly troubling, both in childhood and in adulthood. In this study, we report results obtained in the first epigenome-wide association study ...
  • From genetics to epigenetics: new perpectives in Tourette Syndrome research 
    Pagliaroli, Luca; Vető, Borbála; Arányi, Tamás; Barta, Csaba (2016)
  • Genetic association signal near NTN4 in Tourette Syndrome 
    Paschou, Peristera; Yu, Dongmei; Gerber, Gloria; Evans, Patrick; Tsetsos, Fotis; Davis, LK; Karagiannidis, I; Chaponis, J; Gamazon, E; Mueller-Vahl, K; Stuhrmann, M; Schloegelhofer, M; Stamenkovic, M; Hebebrand, J; Noethen, M; Nagy, Péter; Barta, Csaba; Tarnok, Zsanett; Rizzo, R; Depienne, C; Worbe, Y; Hartmann, A; Cath, DC; Budman, CL; Sandor, P; Barr, C; Wolanczyk, T; Singer, H; Chou, IC; Grados, M; Posthuma, D; Rouleau, GA; Aschauer, H; Freimer, NB; Pauls, DL; Cox, NJ; Mathews, CA; Scharf, JM (2014)
  • Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies 
    Yu, Dongmei; Sul, Jae Hoon; Tsetsos, Fotis; Nawaz, Muhammad S; Huang, Alden Y; Zelaya, Ivette; Illmann, Cornelia; Osiecki, Lisa; Darrow, Sabrina M; Hirschtritt, Matthew E; Greenberg, Erica; Muller-Vahl, Kirsten R; Stuhrmann, Manfred; Dion, Yves; Rouleau, Guy; Aschauer, Harald; Stamenkovic, Mara; Schlögelhofer, Monika; Sandor, Paul; Barr, Cathy L.; Grados, Marco; Singer, Harvey S; Nöthen, Markus M; Hebebrand, Johannes; Hinney, Anke; King, Robert A.; Fernandez, Thomas V; Barta, Csaba; Tarnok, Zsanett; Nagy, Péter; Depienne, Christel; Worbe, Yulia; Hartmann, Andreas; Budman, Cathy L; Rizzo, Renata; Lyon, Gholson J; McMahon, William M; Batterson, James R; Cath, Danielle C; Malaty, Irene A; Okun, Michael S; Berlin, Cheston; Woods, Douglas W; Lee, Paul C; Jankovic, Joseph; Robertson, Mary M; Gilbert, Donald L; Brown, Lawrence W; Coffey, Barbara J; Dietrich, Andrea; Hoekstra, Pieter J; Kuperman, Samuel; Zinner, Samuel H; Luðvigsson, Pétur; Sæmundsen, Evald; Thorarensen, Ólafur; Atzmon, Gil; Barzilai, Nir; Wagner, Michael; Moessner, Rainald; Ophoff, Roel; Pato, Carlos N; Pato, Michele T; Knowles, James A; Roffman, Joshua L; Smoller, Jordan W; Buckner, Randy L; Willsey, A. Jeremy; Tischfield, Jay A; Heiman, Gary A; Stefansson, Hreinn; Stefansson, Kári; Posthuma, Danielle; Cox, Nancy J; Pauls, David L; Freimer, Nelson B; Neale, Benjamin M; Davis, Lea K; Paschou, Peristera; Coppola, Giovanni; Mathews, Carol A; Scharf, Jeremiah M (2019)
  • Multivariate Analysis of Dopaminergic Gene Variants as Risk Factors of Heroin Dependence 
    Vereczkei, Andrea; Demetrovics, Zsolt; Székely, Anna; Sárközy, Péter; Antal, Péter; Szilágyi, Ágnes; Sasvári-Székely, Mária; Barta, Csaba (2013)
  • New insights and perspectives on the genetics of obsessive-compulsive disorder 
    Zai, G; Barta, Csaba; Cath, D; Eapen, V; Geller, D; Grünblatt, E (2019)
    Psychiatric genetic research has exploded in search of polygenic risk factors over the past decade, but because of the complexity and heterogeneity of mental illnesses, using the current understanding of the genome has not ...
  • Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification 
    Theodoropoulou M; Barta, Csaba; Szoke M; Guttman, András; Staub M; Niederland T; Sólyom, János; Fekete, György; Sasvári-Székely, Mária (2001)
  • Psychiatric comorbidity in treatment-seeking substance use disorder patients with and without attention deficit hyperactivity disorder: results of the IASP study. 
    van Emmerik-van Oortmerssen, K; van de Glind ,G; Koeter,MW; Allsop, S; Auriacombe, M; Barta, Csaba; Bu, ETH; Burren,Y; Carpentier, PJ; Carruthers, S; Casas1, M; Demetrovics, Zsolt; Dom, G; Faraone, SV; Fatseas, M; Franck, J; Johnson, B; Kapitány-Fövény, Máté; Kaye, S; Konstenius, M; Levin, FR; Moggi, F; Møller, M; Ramos-Quiroga, A; Schillinger, A; Skutle, A; Verspreet, S; IASP research group; van den Brink, W; Schoevers, RA (2014)
    AIMS: To determine comorbidity patterns in treatment-seeking substance use disorder (SUD) patients with and without adult attention deficit hyperactivity disorder (ADHD), with an emphasis on subgroups defined by ADHD ...
  • Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome 
    Huang AY; Yu D; Davis LK; Sul JH; Tsetsos F; Ramensky V; Zelaya I; Ramos EM; Osiecki L; Chen JA; McGrath LM; Illmann C; Sandor P; Barr CL; Grados M; Singer HS; Nothen MM; Hebebrand J; King RA; Dion Y; Rouleau G; Budman CL; Depienne C; Worbe Y; Hartmann A; Muller-Vahl KR; Stuhrmann M; Aschauer H; Stamenkovic M; Schloegelhofer M; Konstantinidis A; Lyon GJ; McMahon WM; Barta, Csaba; Tárnok, Zsanett; Nagy, Péter; Batterson JR; Rizzo R; Cath DC; Wolanczyk T; Berlin C; Malaty IA; Okun MS; Woods DW; Rees E; Pato CN; Pato MT; Knowles JA; Posthuma D; Pauls DL; Cox NJ; Neale BM; Freimer NB; Paschou P; Mathews CA; Scharf JM; Coppola G; Tourette Syndrome Association International Consortium for Genetics (TSAICG); Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI) (2017)
    Tourette syndrome (TS) is a model neuropsychiatric disorder thought to arise from abnormal development and/or maintenance of cortico-striato-thalamo-cortical circuits. TS is highly heritable, but its underlying genetic ...
  • Riluzole Attenuates L-DOPA-Induced Abnormal Involuntary Movements Through Decreasing CREB1 Activity 
    Pagliaroli, Luca; Widomska, Joanna; Nespoli, Ester; Hildebrandt, Tobias; Barta, Csaba; Glennon, Jeffrey; Hengerer, Bastian; Poelmans, Geert (2019)
    Chronic administration of L-DOPA, the first-line treatment of dystonic symptoms in childhood or in Parkinson's disease, often leads to the development of abnormal involuntary movements (AIMs), which represent an important ...
  • Screening for Mutations of 21-Hydroxylase Gene in Hungarian Patients with Congenital Adrenal Hyperplasia 
    Ferenczi, A; Garami, Miklós; Kiss, Eszter; Pék, M; Sasvári-Székely, Mária; Barta, Csaba; Sólyom, János; Fekete, György (1999)
    Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders, causing impaired secretion of cortisol and aldosterone from the adrenal cortex, with subsequent overproduction of adrenal androgens. ...
  • Support of the histaminergic hypothesis in tourette syndrome: Association of the histamine decarboxylase gene in a large sample of families 
    Karagiannidis, I; Dehning, S; Sandor, P; Tarnok, Z; Rizzo, R; Wolanczyk, T; Madruga-Garrido, M; Hebebrand, J; Nöthen, MM; Lehmkuhl, G; Farkas, L; Nagy, P; Szymanska, U; Anastasiou, Z; Stathias, V; Androutsos, C; Tsironi, V; Koumoula, A; Barta, Csaba; Zill, P; Mir, P; Müller, N; Barr, C; Paschou, P (2013)
    Background: Gilles de la Tourette Syndrome is a neurodevelopmental disorder that is caused by the interaction of environment with a complex genetic background. The genetic etiology of the disorder remains, so far, elusive, ...
  • Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology 
    Alexander J; Potamianou H; Xing JC; Deng L; Karagiannidis I; Tsetsos F; Drineas P; Tarnok Z; Rizzo R; Wolanczyk T; Farkas L; Nagy P; Szymanska U; Androutsos C; Tsironi V; Koumoulas A; Barta, Csaba; Sandor P; Barr CL; Tischfield J; Paschou P; Heiman GA; Georgitsi M (2016)
    Although the genetic basis of Tourette Syndrome (TS) remains unclear, several candidate genes have been implicated. Using a set of 382 TS individuals of European ancestry we investigated four candidate genes for TS (HDC, ...
  • The Genetics of Problem and Pathological Gambling 
    Gyollai, Ágoston Zsolt; Griffiths, MD; Barta, Csaba; Vereczkei, Andrea; Urbán, Róbert; Kun, Bernadette; Kökönyei, Gyöngyi; Székely, Anna; Sasvári-Székely, Mária; Blum, K; Demetrovics, Zsolt (2014)
    Background and aims: The primary aim of the present review was to summarize the findings of genetic studies conducted on problem and pathological gambling. Method: Literature searches were conducted using PubMed, Medline ...