Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mathilde van Oudenaren"'
Autor:
Esther D.A. van Duin, Johannes G. Ramaekers, Jacobus F.A. Jansen, Mathilde van Oudenaren, Janneke Zinkstok, Claudia Vingerhoets, Therese van Amelsvoort, Desmond H. Y. Tse, Grainne M. McAlonan, Dennis Hernaus
Publikováno v:
Journal of Psychopharmacology, 34(8):0269881120922977, 856-863. SAGE Publications Ltd
Journal of Psychopharmacology (Oxford, England)
Journal of Psychopharmacology (Oxford, England)
Aims: 22q11.2 deletion syndrome (22q11.2DS) is associated with impaired cognitive functioning. Glutamatergic pathways have been linked with cognition and are hypothesized to be disrupted in 22q11.2DS patients, possibly ‘shifting’ the excitatory (
Autor:
Therese van Amelsvoort, Lisa D. Palmer, Jacob Vorstman, Annick Vogels, Jan Booij, Ania M Fiksinski, Liewe de Haan, Esther D.A. van Duin, L. J. M. Evers, Claudia Vingerhoets, Elfi Vergaelen, Genetic Risk, Ann Swillen, Anne S. Bassett, Carin J. Meijer, Oswald J.N. Bloemen, Elemi J. Breetvelt, Mathilde van Oudenaren, Erik Boot
Publikováno v:
British Journal of Psychiatry, 215(5), 661-667. Cambridge University Press
British journal of psychiatry, 215(5), 661-667. Royal College of Psychiatrists
British journal of psychiatry, 215(5), 661-667. Royal College of Psychiatrists
Background22q11.2 deletion syndrome (22q11DS), one of the most common recurrent copy number variant disorders, is associated with dopaminergic abnormalities and increased risk for psychotic disorders.AimsGiven the elevated prevalence of substance use
Autor:
J.G. Ramaekers, Desmond H. Y. Tse, Claudia Vingerhoets, Mathilde van Oudenaren, Oswald J.N. Bloemen, Jaap Janssen, Therese van Amelsvoort, Dennis Hernaus, Esther D. A. van Duin, Grainne M. McAlonan
Publikováno v:
Biological Psychiatry. 83:S198-S199
Autor:
Therese van Amelsvoort, Mathilde van Oudenaren, Dennis Hernaus, Jaap Janssen, Grainne M. McAlonan, Claudia Vingerhoets, Esther D.A. van Duin, J.G. Ramaekers, Desmond H. Y. Tse, Oswald J.N. Bloemen
Publikováno v:
Schizophrenia Bulletin
Background 22q11.2 deletion syndrome (22q11DS) is characterized by a microdeletion on the long arm of chromosome 22. The clinical phenotype of this syndrome is highly variable but symptoms include cognitive impairment, heart malformations, auto-immun