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of 30
pro vyhledávání: '"Siegfried Tuinier"'
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
Publikováno v:
World Journal of Biological Psychiatry, 5, 49-53. Taylor & Francis Ltd
This paper describes two cases with khat- and two with psilocybin-induced psychoses and draws attention to the medical and social consequences of the use of these drugs.Two male patients are presented who developed relapsing and short-lasting psychot
Publikováno v:
Acta Neuropsychiatrica, 15, 32-37. Cambridge University Press
Prader–Willi syndrome (PWS) is a genetically determined disorder associated with the loss of the paternal contribution to the proximal part of the long arm of chromosome 15. Its pathophysiology is dominated by hypothalamic dysfunctions. The psychop
Publikováno v:
Journal of Applied Research in Intellectual Disabilities, 14, 147-154. Wiley-Blackwell Publishing Ltd
Cyclic changes in behaviour and mood which do not meet the criteria for bipolar affective disorder have been reported in people with intellectual disability (ID) since the beginning of the twentieth century. The present study postulates a functional