M J Descheemaeker

Summary

Affiliation: Katholieke Universiteit Leuven
Country: Belgium

Publications

  1. ncbi Behavioural, academic and neuropsychological profile of normally gifted Neurofibromatosis type 1 children
    M J Descheemaeker
    Centre for Human Genetics, University of Leuven, Leuven, Belgium
    J Intellect Disabil Res 49:33-46. 2005
  2. ncbi Psychotic disorders in Prader-Willi syndrome
    A Vogels
    Center for Human Genetics, University of Leuven, Leuven, Belgium
    Am J Med Genet A 127:238-43. 2004
  3. ncbi Personality profiles of children and adolescents with neurofibromatosis type 1
    P Prinzie
    Department of Educational Sciences, University of Leuven, Leuven, Belgium
    Am J Med Genet A 118:1-7. 2003

Collaborators

  • K Devriendt
  • A Vogels
  • P Prinzie
  • E Legius
  • J P Fryns
  • M De Hert
  • V Govers
  • J-P Fryns
  • L M G Curfs
  • G J T Haselager
  • T Cleymans
  • W Hellinckx
  • P Onghena
  • C F M van Lieshout

Detail Information

Publications3

  1. ncbi Behavioural, academic and neuropsychological profile of normally gifted Neurofibromatosis type 1 children
    M J Descheemaeker
    Centre for Human Genetics, University of Leuven, Leuven, Belgium
    J Intellect Disabil Res 49:33-46. 2005
    ..In the present study the neuropsychological, academic and social-emotional profiles were examined in Neurofibromatosis type 1 (NF1) children...
  2. ncbi Psychotic disorders in Prader-Willi syndrome
    A Vogels
    Center for Human Genetics, University of Leuven, Leuven, Belgium
    Am J Med Genet A 127:238-43. 2004
    ..The presence of precipitating stress factors and a prodromal phase with physiological symptoms was reported in all patients. Current diagnostic categories do not allow an unequivocal psychiatric diagnosis...
  3. ncbi Personality profiles of children and adolescents with neurofibromatosis type 1
    P Prinzie
    Department of Educational Sciences, University of Leuven, Leuven, Belgium
    Am J Med Genet A 118:1-7. 2003
    ..Personality characteristics were similar for children with maternally or paternally inherited NF1, or for children with a new mutation. There was no association with gender, the severity of medical and cosmetic problems, and IQ...