Willem M A Verhoeven

Summary

Country: The Netherlands

Publications

  1. doi request reprint Beta-propeller protein-associated neurodegeneration (BPAN), a rare form of NBIA: Novel mutations and neuropsychiatric phenotype in three adult patients
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands Erasmus University Medical Centre, Department of Psychiatry, Rotterdam, The Netherlands Electronic address
    Parkinsonism Relat Disord 20:332-6. 2014
  2. doi request reprint Kleefstra syndrome in three adult patients: further delineation of the behavioral and neurological phenotype shows aspects of a neurodegenerative course
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Am J Med Genet A 155:2409-15. 2011
  3. doi request reprint Phelan-McDermid syndrome: clinical report of a 70-year-old woman
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Am J Med Genet A 161:158-61. 2013
  4. doi request reprint Hypersociability in the behavioral phenotype of 17q21.31 microdeletion syndrome
    Jos I M Egger
    Centre of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands
    Am J Med Genet A 161:21-6. 2013
  5. doi request reprint Behavioural phenotype of a patient with a de novo 1.2 Mb chromosome 4q25 microdeletion
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Eur J Med Genet 56:331-5. 2013
  6. doi request reprint Behavioral phenotype in the 9q subtelomeric deletion syndrome: a report about two adult patients
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Am J Med Genet B Neuropsychiatr Genet 153:536-41. 2010
  7. doi request reprint A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsy
    Willem M A Verhoeven
    Centre of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands
    Eur J Med Genet 55:358-61. 2012
  8. doi request reprint Cerebellar cognitive affective syndrome and autosomal recessive spastic ataxia of charlevoix-saguenay: a report of two male sibs
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Psychopathology 45:193-9. 2012

Collaborators

Detail Information

Publications8

  1. doi request reprint Beta-propeller protein-associated neurodegeneration (BPAN), a rare form of NBIA: Novel mutations and neuropsychiatric phenotype in three adult patients
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands Erasmus University Medical Centre, Department of Psychiatry, Rotterdam, The Netherlands Electronic address
    Parkinsonism Relat Disord 20:332-6. 2014
    ..The clinical picture and imaging hallmarks are often highly suggestive and should lead to suspect this specific disorder. However, the identification of a WDR45 mutation is needed for a definite diagnosis of BPAN. ..
  2. doi request reprint Kleefstra syndrome in three adult patients: further delineation of the behavioral and neurological phenotype shows aspects of a neurodegenerative course
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Am J Med Genet A 155:2409-15. 2011
    ..In addition, the utility of uncritical use of a classificatory diagnostic approach is discussed in the context of the motor and motivational disturbances that are prominent in this syndrome...
  3. doi request reprint Phelan-McDermid syndrome: clinical report of a 70-year-old woman
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Am J Med Genet A 161:158-61. 2013
    ....
  4. doi request reprint Hypersociability in the behavioral phenotype of 17q21.31 microdeletion syndrome
    Jos I M Egger
    Centre of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands
    Am J Med Genet A 161:21-6. 2013
    ..31 microdeletion syndrome, preliminary evidence for hypersocial behavior with a high level of frustration tolerance was found that may be implicated in its behavioral phenotype...
  5. doi request reprint Behavioural phenotype of a patient with a de novo 1.2 Mb chromosome 4q25 microdeletion
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Eur J Med Genet 56:331-5. 2013
    ..To the authors knowledge, this is the first report of a de novo 4q25 microdeletion that presents with a specific behavioural phenotype...
  6. doi request reprint Behavioral phenotype in the 9q subtelomeric deletion syndrome: a report about two adult patients
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Am J Med Genet B Neuropsychiatr Genet 153:536-41. 2010
    ..It is concluded that the proposed behavioral phenotype of 9qSTDS comprises at least an erratic sleep pattern and an enduring severe apathy...
  7. doi request reprint A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsy
    Willem M A Verhoeven
    Centre of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands
    Eur J Med Genet 55:358-61. 2012
    ..MRI-scanning of the brain showed no abnormalities. To the authors knowledge, this is the first report of a de novo 8q12.3q13.2 microdeletion syndrome that presents with ESES/CSWS...
  8. doi request reprint Cerebellar cognitive affective syndrome and autosomal recessive spastic ataxia of charlevoix-saguenay: a report of two male sibs
    Willem M A Verhoeven
    Vincent van Gogh Institute for Psychiatry, Centre of Excellence for Neuropsychiatry, Venray, The Netherlands
    Psychopathology 45:193-9. 2012
    ..Cerebellar disorders in general may be accompanied by the cerebellar cognitive affective syndrome (CCAS) which presents with disturbances of executive functioning, spatial cognition, linguistic capacities, and affect...