M C F Gerrits

Summary

Publications

  1. ncbi Pediatric writer's cramp in myoclonus-dystonia: maternal imprinting hides positive family history
    M C F Gerrits
    Department of Neurology, Academic Medical Centre, University of Amsterdam, The Netherlands
    Eur J Paediatr Neurol 13:178-80. 2009
  2. ncbi Distal myoclonus and late onset in a large Dutch family with myoclonus-dystonia
    E M J Foncke
    Department of Neurology, Academic Medical Centre, University of Amsterdam, The Netherlands
    Neurology 67:1677-80. 2006
  3. ncbi Myoclonus-dystonia: clinical and genetic evaluation of a large cohort
    K Ritz
    Department of Neurology, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands
    J Neurol Neurosurg Psychiatry 80:653-8. 2009
  4. ncbi Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia
    M C F Gerrits
    Department of Neurology, Academic Medical Centre, University of Amsterdam, The Netherlands
    Neurology 66:759-61. 2006

Collaborators

  • C Klein
  • L J Ozelius
  • E M J Foncke
  • K Ritz
  • F Baas
  • M A J Tijssen
  • F Van Ruissen
  • C van der Linden
  • W Vandenberghe
  • J D Speelman
  • M D I Vergouwen
  • B R Bloem
  • R Crols
  • C C Tijssen
  • K Hedrich

Detail Information

Publications4

  1. ncbi Pediatric writer's cramp in myoclonus-dystonia: maternal imprinting hides positive family history
    M C F Gerrits
    Department of Neurology, Academic Medical Centre, University of Amsterdam, The Netherlands
    Eur J Paediatr Neurol 13:178-80. 2009
    ..Due to maternal imprinting the family history appeared initially negative for M-D. In children with writer's cramp screening of the SGCE gene should be considered, even with a negative family history...
  2. ncbi Distal myoclonus and late onset in a large Dutch family with myoclonus-dystonia
    E M J Foncke
    Department of Neurology, Academic Medical Centre, University of Amsterdam, The Netherlands
    Neurology 67:1677-80. 2006
    ..Five of 14 asymptomatic mutation carriers who inherited the mutation from their mother showed minimal axial dystonia, arguing against a maternal imprinting mechanism...
  3. ncbi Myoclonus-dystonia: clinical and genetic evaluation of a large cohort
    K Ritz
    Department of Neurology, Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands
    J Neurol Neurosurg Psychiatry 80:653-8. 2009
    ..The lack of stringent clinical inclusion criteria and limitations of mutation screens by direct sequencing might explain this observation...
  4. ncbi Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia
    M C F Gerrits
    Department of Neurology, Academic Medical Centre, University of Amsterdam, The Netherlands
    Neurology 66:759-61. 2006
    ..Positive family history and truncal myoclonus were independent prognostic factors. Early disease onset, onset with both myoclonus and dystonia, and axial dystonia were detected significantly more often in the mutation carriers...