Karlien Dhondt

Summary

Affiliation: Ghent University
Country: Belgium

Publications

  1. doi request reprint Abnormal sleep architecture and refractory nocturnal enuresis
    Karlien Dhondt
    Pediatric Sleep Centre, Ghent University Hospital, Ghent, Belgium
    J Urol 182:1961-5. 2009
  2. doi request reprint Hypocretin-1 deficiency in a girl with ROHHAD syndrome
    Karlien Dhondt
    Pediatric Sleep Centre, Centre for Neurophysiological Monitoring Unit, Department of Pediatrics, Ghent University Hospital, Ghent, Belgium
    Pediatrics 132:e788-92. 2013
  3. doi request reprint Childhood narcolepsy with partial facial cataplexy: a diagnostic dilemma
    Karlien Dhondt
    Department of Child Neurology, Pediatric Sleep Centre, Ghent University Hospital, De Pintelaan 185, B 9000 Ghent, Belgium
    Sleep Med 10:797-8. 2009
  4. pmc Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster
    Helene Verhelst
    Department of Paediatric Neurology, Ghent University Hospital, De Pintelaan 185, B 9000 Gent, Belgium
    Eur J Paediatr Neurol 15:163-6. 2011

Collaborators

Detail Information

Publications4

  1. doi request reprint Abnormal sleep architecture and refractory nocturnal enuresis
    Karlien Dhondt
    Pediatric Sleep Centre, Ghent University Hospital, Ghent, Belgium
    J Urol 182:1961-5. 2009
    ..Children with enuresis are generally believed to have sleep that is too deep with decreased arousability. We investigated sleep characteristics in children with refractory nocturnal enuresis...
  2. doi request reprint Hypocretin-1 deficiency in a girl with ROHHAD syndrome
    Karlien Dhondt
    Pediatric Sleep Centre, Centre for Neurophysiological Monitoring Unit, Department of Pediatrics, Ghent University Hospital, Ghent, Belgium
    Pediatrics 132:e788-92. 2013
    ..The diagnosis was confirmed by showing an absence of hypocretin-1 in the cerebrospinal fluid. We discuss potential pathophysiological implications as well as symptomatic treatment options. ..
  3. doi request reprint Childhood narcolepsy with partial facial cataplexy: a diagnostic dilemma
    Karlien Dhondt
    Department of Child Neurology, Pediatric Sleep Centre, Ghent University Hospital, De Pintelaan 185, B 9000 Ghent, Belgium
    Sleep Med 10:797-8. 2009
    ..The first symptoms were excessive daytime sleepiness, partial facial cataplexy and a serious behavioral disorder. Hypocretin-1 level (Hrt-1) in CSF was undetectable...
  4. pmc Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster
    Helene Verhelst
    Department of Paediatric Neurology, Ghent University Hospital, De Pintelaan 185, B 9000 Gent, Belgium
    Eur J Paediatr Neurol 15:163-6. 2011
    ..Moreover, array-comparative genomic hybridization in this patient revealed an inherited microdeletion in chromosomeband 6p21.32, including the HLA-DPB1 and HLA-DPB2 genes. The clinical relevance of this microdeletion is discussed...