Pharmacological Interventions for the MATRICS Cognitive Domains in Schizophrenia: What’s the Evidence?

por Vingerhoets, Wilhelmina A. M., Bloemen, Oswald J. N., Bakker, Geor, van Amelsvoort, Therese A. M. J.
Publicado 2013

Triple X syndrome: Psychiatric disorders and impaired social functioning as a risk factor

por Otter, Maarten, Campforts, Bea C. M., Stumpel, Constance T. R. M., van Amelsvoort, Thérèse A. M. J., Drukker, Marjan
Publicado 2022

AMPT-induced monoamine depletion in humans: evaluation of two alternative [(123)I]IBZM SPECT procedures

por Boot, Erik, Booij, Jan, Hasler, Gregor, Zinkstok, Janneke R., de Haan, Lieuwe, Linszen, Don H., van Amelsvoort, Thérèse A.
Publicado 2008

Post-traumatic stress in adults with 22q11.2 deletion syndrome

por von Scheibler, Emma N. M. M., van Amelsvoort, Thérèse A. M. J., Vingerhoets, Claudia, van Eeghen, Agnies M., Boot, Erik
Publicado 2022

Glutamatergic markers, age, intellectual functioning and psychosis in 22q11 deletion syndrome

por Evers, Laurens J. M., van Amelsvoort, Therese A. M. J., Bakker, Jaap A., de Koning, Mariken, Drukker, Marjan, Curfs, Leopold M. G.
Publicado 2015

Social functioning and emotion recognition in adults with triple X syndrome

por Otter, Maarten, Crins, Peter M. L., Campforts, Bea C. M., Stumpel, Constance T. R. M., van Amelsvoort, Thérèse A. M. J., Vingerhoets, Claudia
Publicado 2021

Altered subcortical and cortical brain morphology in adult women with 47,XXX: a 7-Tesla magnetic resonance imaging study

por Serrarens, Chaira, Otter, Maarten, Campforts, Bea C. M., Stumpel, Constance T. R. M., Jansma, Henk, van Amelsvoort, Thérèse A. M. J., Vingerhoets, Claudia
Publicado 2022

The muscarinic M(1) receptor modulates associative learning and memory in psychotic disorders

por Bakker, Geor, Vingerhoets, Claudia, Bloemen, Oswald J.N., Sahakian, Barbara J., Booij, Jan, Caan, Matthan W.A., van Amelsvoort, Thérèse A.M.J.
Publicado 2020

The Relationships between Dopaminergic, Glutamatergic, and Cognitive Functioning in 22q11.2 Deletion Syndrome: A Cross-Sectional, Multimodal (1)H-MRS and (18)F-Fallypride PET Study

por van Hooijdonk, Carmen F. M., Tse, Desmond H. Y., Roosenschoon, Julia, Ceccarini, Jenny, Booij, Jan, van Amelsvoort, Therese A. M. J., Vingerhoets, Claudia
Publicado 2022

Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome

por van Beveren, Nico J. M., Krab, Lianne C., Swagemakers, Sigrid, Buitendijk, Gabriella, Boot, Erik, van der Spek, Peter, Elgersma, Ype, van Amelsvoort, Therese A. M. J.
Publicado 2012

Transitional psychiatry in the Netherlands: Experiences and views of mental health professionals

por Gerritsen, Suzanne E., Dieleman, Gwendolyn C., Beltman, Marieke A. C., Tangenbergh, Afke A. M., Maras, Athanasios, van Amelsvoort, Therese A. M. J., van Staa, AnneLoes
Publicado 2019

Correction: Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome

por van Beveren, Nico J. M., Krab, Lianne C., Swagemakers, Sigrid, Buitendijk, Gabriëe H.S., Boot, Erik, van der Spek, Peter, Elgersma, Ype, van Amelsvoort, Therese A. M. J.
Publicado 2012

Lower striatal dopamine D(2/3 )receptor availability in obese compared with non-obese subjects

por de Weijer, Barbara A, van de Giessen, Elsmarieke, van Amelsvoort, Thérèse A, Boot, Erik, Braak, Breg, Janssen, Ignace M, van de Laar, Arnold, Fliers, Eric, Serlie, Mireille J, Booij, Jan
Publicado 2011

Resting-state functional connectivity in adults with 47,XXX: a 7 Tesla MRI study

por Serrarens, Chaira, Kashyap, Sriranga, Riveiro-Lago, Laura, Otter, Maarten, Campforts, Bea C M, Stumpel, Constance T R M, Jansma, Henk, Linden, David E J, van Amelsvoort, Thérèse A M J, Vingerhoets, Claudia
Publicado 2022

Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review

por von Scheibler, Emma N.M.M., van Eeghen, Agnies M., de Koning, Tom J., Kuijf, Mark L., Zinkstok, Janneke R., Müller, Annelieke R., van Amelsvoort, Thérèse A.M.J., Boot, Erik
Publicado 2022

Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology

por Morrison, Sinead, Chawner, Samuel J. R. A., van Amelsvoort, Therese A. M. J., Swillen, Ann, Vingerhoets, Claudia, Vergaelen, Elfi, Linden, David E. J., Linden, Stefanie, Owen, Michael J., van den Bree, Marianne B. M.
Publicado 2020

Cortical Morphology Differences in Subjects at Increased Vulnerability for Developing a Psychotic Disorder: A Comparison between Subjects with Ultra-High Risk and 22q11.2 Deletion...

por Bakker, Geor, Caan, Matthan W. A., Vingerhoets, Wilhelmina A. M., da Silva- Alves, Fabiana, de Koning, Mariken, Boot, Erik, Nieman, Dorien H., de Haan, Lieuwe, Bloemen, Oswald J., Booij, Jan, van Amelsvoort, Thérèse A. M. J.
Publicado 2016

Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study

por von Scheibler, Emma N. M. M., van der Valk Bouman, Emy S., Nuijts, Myrthe A., Bauer, Noël J. C., Berendschot, Tos T. J. M., Vermeltfoort, Pit, Bok, Levinus A., van Eeghen, Agnies M., Houben, Michiel L., van Amelsvoort, Thérèse A. M. J., Boot, Erik, van Egmond‐Ebbeling, Michelle B.
Publicado 2021

To continue or not to continue? Antipsychotic medication maintenance versus dose-reduction/discontinuation in first episode psychosis: HAMLETT, a pragmatic multicenter single-blind...

por Begemann, Marieke J. H., Thompson, Ilse A., Veling, Wim, Gangadin, Shiral S., Geraets, Chris N. W., van ‘t Hag, Erna, Müller-Kuperus, Sanne J., Oomen, Priscilla P., Voppel, Alban E., van der Gaag, Mark, Kikkert, Martijn J., Van Os, Jim, Smit, H. Filip E., Knegtering, Rikus H., Wiersma, Sybren, Stouten, Luyken H., Gijsman, Harm J., Wunderink, Lex, Staring, Anton B. P., Veerman, Selene R. T., Mahabir, Amrita G. S., Kurkamp, Jörg, Pijnenborg, Gerdina H. M., Veen, Natalie D., Marcelis, Machteld, Grootens, Koen P., Faber, Gunnar, van Beveren, Nico J., Been, Agaath, van den Brink, Truus, Bak, Maarten, van Amelsvoort, Therese A. M. J., Ruissen, Andrea, Blanke, Christine, Groen, Karin, de Haan, Lieuwe, Sommer, Iris E. C.
Publicado 2020

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

por Guo, Tingwei, Repetto, Gabriela M., McDonald McGinn, Donna M., Chung, Jonathan H., Nomaru, Hiroko, Campbell, Christopher L., Blonska, Anna, Bassett, Anne S., Chow, Eva W.C., Mlynarski, Elisabeth E., Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E., Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E., Digilio, M. Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E., Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E., Tassone, Flora, Simon, Tony J., van Duin, Esther D.A., van Amelsvoort, Thérèse A., Kates, Wendy R., Zackai, Elaine, Johnston, H. Richard, Cutler, David J., Agopian, A.J., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Emanuel, Beverly S., Morrow, Bernice E.
Publicado 2017