Internationale Konsenserklärung zu Screening, Diagnostik und Behandlung von Jugendlichen und Heranwachsenden mit Aufmerksamkeitsdefizit-/Hyperaktivitätsstörung und gleichzeitigen Störungen durch Substanzgebrauch

Autor: Franz Moggi, Sharon Rabinovitz, Søren Dalsgaard, Wim van den Brink, Ortal Slobodin, Rainer Thomasius, Stephen V. Faraone, Marianne Post, Michiel W van Kernebeek, Florence Vorspan, Falk Kiefer, John Kasinathan, Mathias Luderer, J Antoni Ramos-Quiroga, Wouter G. Staal, Máté Kapitány-Fövény, María C. Vélez-Pastrana, Annabeth P. Groenman, Csaba Barta, Miguel Casas, Renske Spijkerman, Rafael A. González, Gergely Mészáros, Brian Johnson, Heval Ozgen, Michael Kaess, Abu Shafi, Geert Dom, Tobias Banaschewski, Johan Franck, Ilse Truter, Constanza Daigre Blanco, Sabine Vollstädt-Klein, Martin Holtmann, Sharlene Kaye, Giovanni Martinotti, Vincent M. Hendriks, Jesse T Young, Frieda Matthys, Ashmita P Munasur-Naidoo, Arnt S A Schellekens, Alex Begeman, Lara Grau-López, Cleo L. Crunelle, Maija Konstenius, Zsolt Demetrovics, Valsamma Eapen, Moritz Noack, Romain Icick, Amy Yule, Geurt van de Glind, Regina Sala, Malin Hemphälä, Jacomine den Boer, Frances R. Levin

Publikováno v: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie. 50:54-67

Zusammenfassung. Hintergrund: Eine Aufmerksamkeitsdefizit-/Hyperaktivitätsstörung (ADHS) im Kindesalter stellt einen Risikofaktor für Substanzmissbrauch und Störungen durch Substanzgebrauch (Substance Use Disorder, SUD) in der Pubertät und dem (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::82ae38130aab85ebd4befb0bb4deb6d6
https://doi.org/10.1024/1422-4917/a000828

The continuing search for an addiction vaccine

Autor: Stuart Blume, M. Heval Ozgen

Publikováno v: Vaccine. 37:5485-5490

Inspired by advances in immunology, in the 1970s scientists began to study the possibilities of mobilizing the human immune system against intruders other than pathogenic viruses and bacteria. In 1972 the suggestion was first made that it might be po

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9711e5f992662159802d211d7faead6
https://doi.org/10.1016/j.vaccine.2019.06.074

International consensus statement for the screening, diagnosis, and treatment of adolescents with concurrent attention-deficit/hyperactivity disorder and substance use disorder

Autor: Arnt S A Schellekens, Geurt van de Glind, Franz Moggi, Cleo L. Crunelle, Csaba Barta, Zsolt Demetrovics, John Kasinathan, Mathias Luderer, Sharon Rabinovitz, Annabeth P. Groenman, Rainer Thomasius, Abu Shafi, María C. Vélez-Pastrana, Geert Dom, Regina Sala, Vincent M. Hendriks, Heval Ozgen, Ilse Truter, Wim van den Brink, Giovanni Martinotti, Alex Begeman, Frieda Matthys, Renske Spijkerman, Tobias Banaschewski, Brian Johnson, Lara Grau-López, J Antoni Ramos-Quiroga, Maija Konstenius, Frances R. Levin, Wouter G. Staal, Johan Franck, Ortal Slobodin, Jesse T Young, Sabine Vollstädt-Klein, Sharlene Kaye, Martin Holtmann, Ashmita P Munasur-Naidoo, Miguel Casas, Søren Dalsgaard, Constanza Daigre Blanco, Valsamma Eapen, Moritz Noack, Romain Icick, Amy Yule, Michael Kaess, Máté Kapitány-Fövény, Florence Vorspan, Falk Kiefer, Stephen V. Faraone, Marianne Post, Gergely Mészáros, Michiel W van Kernebeek, Rafael A. González, Malin Hemphälä, Jacomine den Boer

Publikováno v: European addiction research
Özgen, H, Spijkerman, R, Noack, M, Holtmann, M, Schellekens, A S A, van de Glind, G, Banaschewski, T, Barta, C, Begeman, A, Casas, M, Crunelle, C L, Daigre Blanco, C, Dalsgaard, S, Demetrovics, Z, den Boer, J, Dom, G, Eapen, V, Faraone, S V, Franck, J, González, R A, Grau-López, L, Groenman, A P, Hemphälä, M, Icick, R, Johnson, B, Kaess, M, Kapitány-Fövény, M, Kasinathan, J G, Kaye, S S, Kiefer, F, Konstenius, M, Levin, F R, Luderer, M, Martinotti, G, Matthys, F I A, Meszaros, G, Moggi, F, Munasur-Naidoo, A P, Post, M, Rabinovitz, S, Ramos-Quiroga, J A, Sala, R, Shafi, A, Slobodin, O, Staal, W G, Thomasius, R, Truter, I, van Kernebeek, M W, Velez-Pastrana, M C, Vollstädt-Klein, S, Vorspan, F, Young, J T, Yule, A, van den Brink, W & Hendriks, V 2020, ' International Consensus Statement for the Screening, Diagnosis, and Treatment of Adolescents with Concurrent Attention-Deficit/Hyperactivity Disorder and Substance Use Disorder ', European Addiction Research, vol. 26, no. 4-5, pp. 223-232 . https://doi.org/10.1159/000508385
European Addiction Research, 26(4-5), 223-232. Karger
European Addiction Research, 26, 4-5, pp. 223-232
Zeitschrift für Kinder und Jugendpsychiatrie und Psychotherapie, 50(1), 54-67
European Addiction Research, 26(4-5), 223-232. KARGER
European Addiction Research, 26, 223-232
European addiction research, 26(4-5), 223-232. S. Karger AG

Background: Childhood attention-deficit/hyperactivity disorder (ADHD) is a risk factor for substance misuse and substance use disorder (SUD) in adolescence and (early) adulthood. ADHD and SUD also frequently co-occur in treatment-seeking adolescents,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93232ef7f5f73c7412809ed0b70fbd97
https://hdl.handle.net/10067/1700850151162165141

A Novel 6.14 Mb Duplication of Chromosome 8p21 in a Patient with Autism and Self Mutilation

Autor: Heval Ozgen, Marc J. Eleveld, Wouter G. Staal, Maretha de Jonge, Martin Poot, Frits A. Beemer, John C. K. Barber, Ron Hochstenbach

Publikováno v: Journal of Autism and Developmental Disorders. 39:322-329

Autism spectrum disorders (ASDs) are a group of neurodevelopmental disorders with a strong genetic etiology. Cytogenetic abnormalities have been detected in 5-10% of the patients with autism. In this study, we present the clinical, cytogenetic and ar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::402d1e007757d42c9131d1a54a328493
https://doi.org/10.1007/s10803-008-0627-x

A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts

Autor: E. Kurt, I. Akkol, Sultan Cingoz, M. Apaydin, Mihriban Heval Ozgen, R. B. van der Luijt

Publikováno v: Familial cancer. 12(1)

von Hippel-Lindau (VHL) disease is a hereditary tumor syndrome caused by mutations in the VHL tumor suppressor gene. In a family with VHL, we identified a novel missense mutation (N78D), which affects a fully conserved residue in the VHL protein. Int

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb5e7b0c2e7f79f53d1e01ac1592f2a8
https://pubmed.ncbi.nlm.nih.gov/23224817