Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Siegfried Tuinier"'
Autor:
Oei, T.I.
Publikováno v:
Mededelingenblad van de Nederlandse Vereniging voor Psychoanalyse, 24(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::1cb4a55e177659ee7ccad040ca243344
https://research.tilburguniversity.edu/en/publications/03b07912-b00c-4594-8e8b-4017ed9bf187
https://research.tilburguniversity.edu/en/publications/03b07912-b00c-4594-8e8b-4017ed9bf187
Publikováno v:
Biologics: Targets & Therapy, Vol 2008, Iss Issue 3, Pp 409-417 (2008)
Willem MA Verhoeven1,2, Siegfried Tuinier1, Ineke van der Burgt31Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands; 2Department of Psychiatry, Erasmus University Medical Centre, Rotterdam, The Netherlands; 3Department of Human Geneti
Externí odkaz:
https://doaj.org/article/827bdc653fd24564a392802bebfb16cd
Publikováno v:
Acta neuropsychiatrica. 10(4)
SUMMARYDescription of psychopathological symptoms in mentally retarded subjects is of great heuristic value because of the association with a known genetic disorder as well as the heterogenous and atypical phenomenology. The concept of behavioural ph
Publikováno v:
Psychopathology. 43:63-68
Background:The diagnosis of Rubinstein-Taybi syndrome (RTS) is primarily clinical and based on the characteristic phenotype that is often combined with a variety of somatic anomalies and psychiatric disorders. Sampling and Methods:In this paper, a re
Publikováno v:
Advances in Therapy. 26:170-184
Stimulant medications are the most effective drugs in the treatment of attention-deficit hyperactivity disorder (ADHD) in children and in adults. However, some patients do not respond to this treatment and other patients suffer from adverse effects.
Autor:
Willem M.A. Verhoeven, Siegfried Tuinier, Ellen Wingbermühle, Jos I. M. Egger, Ineke van der Burgt
Publikováno v:
American Journal of Medical Genetics. Part A, 146A, 191-6
American Journal of Medical Genetics. Part A, 146A, 191-196
American Journal of Medical Genetics Part A, 146A(2), 191-196. Wiley-Liss Inc.
American Journal of Medical Genetics. Part A, 146A, 2, pp. 191-196
American Journal of Medical Genetics. Part A, 146A, 2, pp. 191-6
American Journal of Medical Genetics. Part A, 146A, 191-196
American Journal of Medical Genetics Part A, 146A(2), 191-196. Wiley-Liss Inc.
American Journal of Medical Genetics. Part A, 146A, 2, pp. 191-196
American Journal of Medical Genetics. Part A, 146A, 2, pp. 191-6
Contains fulltext : 55786.pdf (Publisher’s version ) (Closed access) Although Noonan syndrome (NS) is a disorder with a relatively high prevalence, virtually no information in adult patients is available about the psychological and psychopathologic
Publikováno v:
Acta Neuropsychiatrica, 19, 244-250
Acta Neuropsychiatrica, 19, 4, pp. 244-250
Acta Neuropsychiatrica, 19, 244-250. Cambridge University Press
Acta Neuropsychiatrica, 19, 4, pp. 244-250
Acta Neuropsychiatrica, 19, 244-250. Cambridge University Press
Background:In both Prader-Willi syndrome (PWS) and 22q11 deletion syndrome [velo-cardio-facial syndrome (VCFS)], an increased risk for psychotic disorders is reported, which are as a rule not included in the behavioural phenotype of these two syndrom
Autor:
Siegfried Tuinier, W.M.A. Verhoeven, Cees Noordam, S.J.H. Duffels, Jos I. M. Egger, B. B. A. de Vries
Publikováno v:
Psychopathology, 40(5), 356-360. Karger
Psychopathology, 40, 356-360
Psychopathology, 40, 5, pp. 356-360
Psychopathology, 40, 356-60
Psychopathology, 40, 5, pp. 356-60
Psychopathology, 40, 356-360
Psychopathology, 40, 5, pp. 356-360
Psychopathology, 40, 356-60
Psychopathology, 40, 5, pp. 356-60
Item does not contain fulltext In this paper a review is presented of the rare combination of Klinefelter's syndrome and Prader-Willi syndrome (PWS) and a second case of this combination with a uniparental disomy (UPD) etiology of PWS is described. P