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Browsing by Author Verhoeven, W.M.A.

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Showing results 1 to 50 of 82
Full TextIssue DateTitleAuthor(s)
2012X-linked Aarskog syndrome: report on a novel FGD1 gene mutation. Executive dysfunction as part of the behavioural phenotypeVerhoeven, W.M.A.; Egger, J.I.M.; Hoogeboom, A.J.M.
2012Executive dysfunctions as part of the behavioural phenotype of Aarskog-Scott syndromeEgger, J.I.M.; Verhoeven, W.M.A.; Janssen, G.T.L.; Aken, L. van; Hoogeboom, A.J.M.
2012A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsyVerhoeven, W.M.A.; Egger, J.I.M.; Feenstra, I.; Leeuw, N. de
2012The neurocognition of alexithymia: evidence from neuropsychological and neuroimaging studiesWingbermühle, P.A.M.; Theunissen, A.W.M.; Verhoeven, W.M.A.; Kessels, R.P.C.; Egger, J.I.M.
2012A de novo microdeletion in chromosome 8q12.3q13.2: association with mild intellectual disability and epilepsy?Verhoeven, W.M.A.; Egger, J.I.M.; Feenstra, I.; Leeuw, N. de
2012Neuropsychologische kenmerken van het Noonan syndroomWingbermühle, P.A.M.; Egger, J.I.M.; Verhoeven, W.M.A.; Burgt, I. van der
2012Polg mutation in a patient with recurrent major depression, cardiomyopathy and ataxiaVerhoeven, W.M.A.; Egger, J.I.M.; Kremer, H.P.H.; Pont, B.J.H.B. de; Marcelis, C.L.M.
2012Social cognition and the behavioural phenotype of 17q21.31 microdeletion syndromeEgger, J.I.M.; Wingbermühle, P.A.M.; Verhoeven, W.M.A.; Dijkman, M.W.; Kessels, R.P.C., et al
2012Autisme en genetische syndromenVerhoeven, W.M.A.; Egger, J.I.M.; Feenstra, I.
2012Cognitive functioning of adults with Noonan syndrome: a case-control studyWingbermühle, P.A.M.; Roelofs, R.L.; Burgt, C.J.A.M. van der; Souren, P.M.; Verhoeven, W.M.A., et al
2012Phelan-McDermid syndrome in two adult brothers: atypical bipolar disorder as its psychopathological phenotype?Verhoeven, W.M.A.; Egger, J.I.M.; Willemsen, M.H.; Leijer, G.J.M. de; Kleefstra, T.
2012Genetic syndromes and the autism spectrumVerhoeven, W.M.A.; Egger, J.I.M.; Feenstra, I.
2012Psychopathology in rare genetic disordersVerhoeven, W.M.A.; Egger, J.I.M.; Brunner, H.G.
2012Autism spectrum disorders and disinhibited behaviours: toward a translational approachVerhoeven, W.M.A.; Egger, J.I.M.
2012Cerebellar Cognitive Affective Syndrome and Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay: A Report of Two Male SibsVerhoeven, W.M.A.; Egger, J.I.M.; Ahmed, A.I.A.; Kremer, H.P.H.; Vermeer, S., et al
2012Affective functioning and social cognition in Noonan syndromeWingbermühle, P.A.M.; Egger, J.I.M.; Verhoeven, W.M.A.; Burgt, C.J.A.M. van der; Kessels, R.P.C.
2012Neuropsychological phenotyping of genetic syndromesEgger, J.I.M.; Koolen, D.A.; Wingbermühle, P.A.M.; Verhoeven, W.M.A.; Kleefstra, T., et al
2011Manganese and acute paranoid psychosis: a case reportVerhoeven, W.M.A.; Egger, J.I.M.; Kuijpers, H.J.H.
2011Schizotypy: Key feature of Klinefelter's syndrome?Verhoeven, W.M.A.; Egger, J.I.M.
2011Recurrent major depression, ataxia, and cardiomyopathy: association with a novel POLG mutation?Verhoeven, W.M.A.; Egger, J.I.; Kremer, H.P.H.; Pont, B.J.H.B. de; Marcelis, C.L.M.
2011Kleefstra Syndrome in Three Adult Patients: Further Delineation of the Behavioral and Neurological Phenotype Shows Aspects of a Neurodegenerative CourseVerhoeven, W.M.A.; Egger, J.I.M.; Vermeulen, K.; Warrenburg, B.P.C. van de; Kleefstra, T.
2011Behavioral neurobiology of aggression: From perception to actionTuinier, S.; Verhoeven, W.M.A.; Egger, J.I.M.
2011Kleefstra syndrome in three adult patients: further delineation of the behavioral and neurological phenotype shows aspects of a neurodegenerative courseVerhoeven, W.M.A.; Egger, J.I.; Vermeulen, K.; Warrenburg, B.P.C. van de; Kleefstra, T.
2011A Patient With a De Novo Distal 22q11.2 Microdeletion and Anxiety DisorderVerhoeven, W.M.A.; Egger, J.I.M.; Brunner, H.G.; Leeuw, N. de
2011Recurrent major depression, ataxia, and cardiomyopathy: association with a novel POLG mutation?Verhoeven, W.M.A.; Egger, J.I.M.; Kremer, H.P.H.; Pont, B.J.H.B. de; Marcelis, C.L.M.
2010Psychiatric profile in Rubinstein-Taybi syndrome : a review and case reportVerhoeven, W.M.A.; Tuinier, S.; Kuijpers, H.J.M.E.; Egger, J.I.; Brunner, H.G.
2010Recurrent schizophrenia-like psychosis as first manifestation of epilepsy: a diagnostic challenge in neuropsychiatry.Verhoeven, W.M.A.; Egger, J.I.; Gunning, W.B.; Bevers, M.; Pont, B.J. de
2010An adult female patient with ring chromosome 21: behavioural phenotype and results of high-resolution molecular characterisationVerhoeven, W.M.A.; Bon, B.W.M. van; Egger, J.I.M.; Hoischen, A.; Doelman, J.C.
2010Behavioral Phenotype in the 9q Subtelomeric Deletion SyndromeVerhoeven, W.M.A.; Kleefstra, T.; Egger, J.I.M.
2010Psychiatric Profile in Rubinstein-Taybi Syndrome. A Review and Case ReportVerhoeven, W.M.A.; Tuinier, S.; Kuijpers, H.J.H.; Egger, J.I.M.; Brunner, H.G.
2010Behavioral phenotype in the 9q subtelomeric deletion syndrome: a report about two adult patients.Verhoeven, W.M.A.; Kleefstra, T.; Egger, J.I.
2010Noonan syndromeWingbermühle, P.A.M.; Burgt, C.J.A.M. van der; Egger, J.I.M.; Verhoeven, W.M.A.
2010Sanfilippo B in an elderly female psychiatric patient: a rare but relevant diagnosis in presenile dementia.Verhoeven, W.M.A.; Csepan, R.; Marcelis, C.L.M.; Lefeber, D.J.; Egger, J.I., et al
2009Sanfilippo B in an elderly female psychiatric patient: a rare but relevant diagnosis in presenile dementiaCsepán, R.; Verhoeven, W.M.A.; Marcelis, C.L.M.; Lefeber, D.J.; Egger, J.I.M., et al
2009A novel duplication of chromosome (13)(q14.1q21.3) in a patient with mental retardation and microcephalyVerhoeven, W.M.A.; Ruiter, E.M.; Egger, J.I.M.; Tuinier, S.; Smeets, D.F.C.M.
2009Avolition in a patient with hypogonadismVerhoeven, W.M.A.; Tuinier, S.; Egger, J.I.M.; Erp, C.A. van; Tuerlings, J.H.A.M.
2009The fetal anticonvulsant syndrome in an adult male: a rare example of violent behaviour in the context of epilepsy related disordersVerhoeven, W.M.A.; Egger, J.I.M.; Tuinier, S.
2009Neuropsychological and behavioural aspects of Noonan syndromeWingbermühle, P.A.M.; Egger, J.I.M.; Burgt, C.J.A.M. van der; Verhoeven, W.M.A.
2009Een algoritme voor psychofarmaca bij verstandelijk gehandicapten: psychiatrische diagnostiek in drie stappenVerhoeven, W.M.A.; Tuinier, S.; Egger, J.I.M.
2008Improving the assessment of executive processes : Behavioural consequences of dysfunctioning in clinical and nonclinical populationsJanssen, G.T.L.; Egger, J.I.M.; Mey, H.R.A. De; Witteman, C.L.M.; Verhoeven, W.M.A.
2008Subsyndromal mood symptoms, cognition, and psychosocial functioning in euthymic bipolar patientsErp Taalman Kip, R.M. van; Egger, J.I.M.; Hartong, E.G.T.M.; Jeuken, J.M.G.; Verhoeven, W.M.A.
2008Chromosomal abnormalities in psychiatry : expanding the diagnostic processVerhoeven, W.M.A.; Tuinier, S.; Egger, J.I.M.
2008The use of alexithymia scales in patients with Noonan SyndromeVerhoeven, W.M.A.; Wingbermühle, P.A.M.; Egger, J.I.M.; Burgt, C.J.A.M. van der; Tuinier, S., et al
2008Oniomania or compulsive buying: An overviewBoermans, J.A.J.; Egger, J.I.M.; Verhoeven, W.M.A.
2008An algorithm for psychotropics for the mentally handicapped : psychiatric diagnosis in three stagesVerhoeven, W.M.A.; Tuinier, S.; Egger, J.I.M.
2008Subsyndromale stemmingsklachten bij euthyme patiënten met bipolaire stoornisErp Taalman Kip, R.M. van; Egger, J.I.M.; Hartong, E.G.T.M.; Jeuken, J.M.G.; Verhoeven, W.M.A.
2008Woede: Een emotie buiten het brein?Tuinier, S.; Verhoeven, W.M.A.; Egger, J.I.M.
2008Noonan syndrome : psychological and psychiatric aspectsVerhoeven, W.M.A.; Wingbermühle, P.A.M.; Egger, J.I.M.; Burgt, C.J.A. van der; Tuinier, S.
2008Response and remission in schizophrenia: The limited value of new remission criteriaTuinier, S.; Eschauzier, J.C.; Egger, J.I.M.; Verhoeven, W.M.A.
2008Noonansyndroom; samenhang met sociaal-cognitieve functies en psychiatrische symptomen?Verhoeven, W.M.A.; Wingbermühle, P.A.M.; Egger, J.I.M.; Burgt, C.J.A.M. van der; Tuinier, S.
Showing results 1 to 50 of 82

 

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