Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Maarten Otter"'
Autor:
Chaira Serrarens, Maarten Otter, Bea C. M. Campforts, Constance T. R. M. Stumpel, Henk Jansma, Thérèse A. M. J. van Amelsvoort, Claudia Vingerhoets
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-10 (2022)
Abstract Background Triple X syndrome (47,XXX) is a relatively common sex chromosomal aneuploidy characterized by the presence of a supernumerary X chromosome in females and has been associated with a variable cognitive, behavioural and psychiatric p
Externí odkaz:
https://doaj.org/article/a0b8a773277249e5aff917214f76c18d
Autor:
Maarten Otter, Bea C. M. Campforts, Constance T. R. M. Stumpel, Thérèse A. M. J. van Amelsvoort, Marjan Drukker
Publikováno v:
European Psychiatry, Vol 66 (2023)
Abstract Background Women with triple X syndrome (TXS) have an extra X chromosome. TXS appeared to be associated with psychiatric disorders in biased or underpowered studies. Aim This study aims to describe the prevalence of psychiatric disorders
Externí odkaz:
https://doaj.org/article/090f47b39f7b40179fb62151f3a08dee
Autor:
Maarten Otter, Peter M. L. Crins, Bea C. M. Campforts, Constance T. R. M. Stumpel, Thérèse A. M. J. van Amelsvoort, Claudia Vingerhoets
Publikováno v:
BJPsych Open, Vol 7 (2021)
Background Triple X syndrome (TXS) is caused by aneuploidy of the X chromosome and is associated with impaired social functioning in children; however, its effect on social functioning and emotion recognition in adults is poorly understood. Aims The
Externí odkaz:
https://doaj.org/article/bda68570f5e54474a8b64577a8d296c6
Autor:
Chaira Serrarens, Sriranga Kashyap, Laura Riveiro-Lago, Maarten Otter, Bea C M Campforts, Constance T R M Stumpel, Henk Jansma, David E J Linden, Thérèse A M J van Amelsvoort, Claudia Vingerhoets
Publikováno v:
Cerebral Cortex, 33(9), 5210-5217. Oxford University Press
Triple X syndrome is a sex chromosomal aneuploidy characterized by the presence of a supernumerary X chromosome, resulting in a karyotype of 47,XXX in affected females. It has been associated with a variable cognitive, behavioral, and psychiatric phe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bbf3b9333064824afab176bc2770f28
https://doi.org/10.1093/cercor/bhac410
https://doi.org/10.1093/cercor/bhac410
Autor:
Maarten Otter, Bea Campforts, Connie TRM Stumpel, Thérèse Van Amelsvoort, Claudia Vingerhoets, Marjan Drukker
Triple X syndrome (TXS, also known as trisomy X or 47,XXX) has been associated with impaired overall neurocognitive functioning in children and relatively young adults. However, neurocognitive functioning in adults with TXS is poorly understood. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9468b7c6f2158d4038a4750158f1490
Autor:
Constance T. R. M. Stumpel, Therese van Amelsvoort, Maarten Otter, Peter M. L. Crins, Claudia Vingerhoets, Bea Campforts
Publikováno v:
Bjpsych open, 7(2):51. Cambridge University Press
BJPsych Open
BJPsych Open
BackgroundTriple X syndrome (TXS) is caused by aneuploidy of the X chromosome and is associated with impaired social functioning in children; however, its effect on social functioning and emotion recognition in adults is poorly understood.AimsThe aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82757bc457fa58c262236f31518071c4
https://cris.maastrichtuniversity.nl/en/publications/c3a026ba-56be-41a0-9b4c-0da58b2e93ad
https://cris.maastrichtuniversity.nl/en/publications/c3a026ba-56be-41a0-9b4c-0da58b2e93ad
Autor:
Chaira Serrarens, Maarten Otter, Bea C.M. Campforts, Constance T.R.M. Stumpel, Henk Jansma, Therese A.M.J. van Amelsvoort, Claudia Vingerhoets
Publikováno v:
Biological Psychiatry. 91:S152
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85ac4906c50190c68eb736b3616becac
https://doi.org/10.1016/j.biopsych.2022.02.396
https://doi.org/10.1016/j.biopsych.2022.02.396
Publikováno v:
Advances in Mental Health and Intellectual Disabilities, 12(1), 1-10. Emerald Group Publishing Ltd.
Purpose The purpose of this paper is to establish the value of clinical genetic diagnostics in the lives of people with an intellectual disability (ID), their families, and their primary and professional caregivers. It has been shown that psychologis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e130a887f43e4e8d99984e6659ed28d4
https://cris.maastrichtuniversity.nl/en/publications/a5309164-41c2-4d94-b571-9d72be0b9aa6
https://cris.maastrichtuniversity.nl/en/publications/a5309164-41c2-4d94-b571-9d72be0b9aa6
Autor:
Rolph Pfundt, Constance T. R. M. Stumpel, Marline Pisters, Yvonne J. Vos, Rutger A.J. Nievelstein, Marijke R. Wevers, Maarten Otter
Publikováno v:
Clinical Case Reports, 5, 8, pp. 1213-1217
Clinical Case Reports, 5(8), 1213-1217. Wiley
Clinical Case Reports, 5, 1213-1217
Clinical Case Reports
Clinical case reports, 5(8), 1213-1217. Wiley
Clinical Case Reports, 5(8), 1213-1217. Wiley
Clinical Case Reports, 5, 1213-1217
Clinical Case Reports
Clinical case reports, 5(8), 1213-1217. Wiley
Contains fulltext : 177363.pdf (Publisher’s version ) (Open Access) Clinical geneticists, neurologists, psychiatrists, and other healthcare providers can learn from this case report that patients with a behavioral phenotype that includes a mild lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da3d0aebae8f174d991ddbd27953901d
https://hdl.handle.net/2066/177363
https://hdl.handle.net/2066/177363
Publikováno v:
American Journal of Psychiatry, 169(1), 96-97
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7db243655dd26fa2a097b657748b7383
https://doi.org/10.1176/appi.ajp.2011.11091382
https://doi.org/10.1176/appi.ajp.2011.11091382