Zobrazeno 1 - 10
of 376
pro vyhledávání: '"W.M.A. Verhoeven"'
Publikováno v:
Acta neuropsychiatrica. 13(1)
SUMMARYKlinefelter syndrome is a genetically determined disorder characterized by an additional X-chromosome. Apart from the phenotypical features, the literature about this disorder mentiones a psychopathological phenotype comprising mainly psychose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7285b9006f1bcf73585486866202fbbb
https://pubmed.ncbi.nlm.nih.gov/26983763
https://pubmed.ncbi.nlm.nih.gov/26983763
Autor:
W.M.A. Verhoeven, S. Tuinier
Publikováno v:
Acta neuropsychiatrica. 11(2)
SummaryNeuropsychiatry or Biological Psychiatry There is an urgent need to reconsider the position of psychiatry within the neurosciences because of the exploding knowledge about the relationship between brain and behaviour and the delay in implement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c0a6231b9dd97136c477a5247ea891b
https://pubmed.ncbi.nlm.nih.gov/26976261
https://pubmed.ncbi.nlm.nih.gov/26976261
Autor:
W.M.A. Verhoeven
Publikováno v:
Acta neuropsychiatrica. 12(4)
SUMMARYSince 1863 psychiatry is dominated by the nosological conceptual paradigm that was further stimulated by the introduction of the DSM-III. This has resulted in an ignorance of the European psychiatric diagnostic tradition and a loss of the nece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32a7a1e4740391694152dae5b71284c9
https://pubmed.ncbi.nlm.nih.gov/26975434
https://pubmed.ncbi.nlm.nih.gov/26975434
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e03e2569159df1a0c1a7bb305166a00
https://pubmed.ncbi.nlm.nih.gov/26971893
https://pubmed.ncbi.nlm.nih.gov/26971893
Autor:
W.M.A. Verhoeven, S. Tuinier
Publikováno v:
Acta neuropsychiatrica. 9(2)
Over the past decades extensive research has been performed on the presumed relationship between neurotransmitter functionality in the central nervous system and psychopathological states. Originally, in the mid-sixties it was hypothesized that depre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8af028a550357604c2fe7954e9aa70f
https://pubmed.ncbi.nlm.nih.gov/26972136
https://pubmed.ncbi.nlm.nih.gov/26972136
Publikováno v:
Neuropraxis. 16:46-52
Noonan syndrome is a genetic disorder, mainly characterized by short stature, facial dysmorphia en congenital heart disease. Intelligence scores are in a wide range, with a mildly lowered average. Development of motor and language functions is often
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e519ca305f88bc06d0a02c8a4c6f40c7
https://doi.org/10.1007/s12474-012-0008-2
https://doi.org/10.1007/s12474-012-0008-2
Publikováno v:
Psychological Medicine, 42, pp. 419-426
Psychological Medicine, 42(2), 419-426. Cambridge University Press
Psychological Medicine, 42, 419-426
Psychological Medicine, 42(2), 419-426. Cambridge University Press
Psychological Medicine, 42, 419-426
BackgroundNoonan syndrome (NS) is a common genetic disorder, characterized by short stature, facial dysmorphia, congenital heart defects and a mildly lowered IQ. Impairments in psychosocial functioning have often been suggested, without, however, sys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::338b9e86bf9b9d3799e13154a632602c
https://hdl.handle.net/2066/108802
https://hdl.handle.net/2066/108802
Autor:
J.I.M. Egger, W.M.A. Verhoeven
Publikováno v:
Neuropraxis, 2010, 64-71
Neuropraxis, 2010, 3, pp. 64-71
Neuropraxis, 2010, 3, pp. 64-71
Item does not contain fulltext Het begin van de neuropsychiatrie zou geplaatst kunnen worden bij de klassieke Griekse geneesheren die reeds de samenhang onderkenden tussen gestoorde hersenfuncties en psychiatrische ziekten. Uit die tijd stammen ook d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83ba41be251f10c3046e81601095dc74
https://doi.org/10.1007/s12474-010-0013-2
https://doi.org/10.1007/s12474-010-0013-2
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d2635d90236ca26eea0dad310b81450
https://doi.org/10.1159/000260045
https://doi.org/10.1159/000260045
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94acd17fcac78b965b5e7b13c85f516b
https://hdl.handle.net/2066/51856
https://hdl.handle.net/2066/51856