Willem M.A. Verhoeven, M.D., Ph.D.

Affiliations: 
1999-2014 Psychiatry Erasmus Medical Center Rotterdam, Rotterdam, Netherlands 
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Parents

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David de Wied grad student 1983
Herman M. van Praag grad student 1983 UMC Utrecht

Collaborators

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Siegfried Tuinier collaborator 2008
Jos I.M. Egger collaborator 2004-2014 Erasmus MC
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Publications

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Verhoeven WMA, Egger JIM, Janssen PKC, et al. (2020) Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene. Bmj Case Reports. 13
Verhoeven WMA, Egger JIM, Jongbloed RE, et al. (2020) A de novo Novel Splice Variant in an Adult Female with Severe Intellectual Disability. International Medical Case Reports Journal. 13: 487-492
Verhoeven WMA, Egger JIM, de Leeuw N. (2020) A longitudinal perspective on the pharmacotherapy of 24 adult patients with Phelan McDermid syndrome. European Journal of Medical Genetics. 63: 103751
Verhoeven W, Egger J, Kipp J, et al. (2019) A novel MBD5 mutation in an intellectually disabled adult female patient with epilepsy: Suggestive of early onset dementia? Molecular Genetics & Genomic Medicine. 7
Verhoeven W, Egger J, Räkers E, et al. (2018) Phenotypic characterization of an older adult male with late-onset epilepsy and a novel mutation in ASXL3 shows overlap with the associated Bainbridge-Ropers syndrome Neuropsychiatric Disease and Treatment. 14: 867-870
Egger JIM, Verhoeven WMA, Groenendijk-Reijenga R, et al. (2017) Phelan-McDermid syndrome due to mutation in an intellectually disabled adult male: successful treatment with lithium. Bmj Case Reports. 2017
Ouwens IMD, Lens CE, Fiolet ATL, et al. (2017) Malaria Fever Therapy for General Paralysis of the Insane: A Historical Cohort Study. European Neurology. 78: 56-62
Verhoeven WMA, Egger JIM, Leeuw Nd. (2017) Differentiated psychopharmacological treatment in three genetic subtypes of 22q11.2 deletion syndrome European Psychiatry. 41
Verhoeven WMA, Egger JIM, Leeuw Nd, et al. (2017) Kleefstra syndrome: Considerations about treatment strategy in 2 patients with a causative Ehmt1 mutation and apathy European Psychiatry. 41
van de Kerkhof NW, Fekkes D, van der Heijden FM, et al. (2016) Cycloid psychoses in the psychosis spectrum: evidence for biochemical differences with schizophrenia. Neuropsychiatric Disease and Treatment. 12: 1927-33
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