K Heuser

Summary

Affiliation: Rikshospitalet University Hospital
Country: Norway

Publications

  1. ncbi request reprint Neuro-ophthalmological findings in sarcoidosis
    Kjell Heuser
    Department of Neurology, Rikshospitalet, University of Oslo, Oslo, Norway
    Acta Ophthalmol Scand 82:723-9. 2004
  2. ncbi request reprint Microvascular decompression for hemifacial spasm: postoperative neurologic follow-up and evaluation of life quality
    K Heuser
    Division for Clinical Neuroscience, Department of Neurology, Rikshospitalet Radiumhospitalet, University of Oslo, Oslo, Norway
    Eur J Neurol 14:335-40. 2007
  3. doi request reprint Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy
    Kjell Heuser
    Department of Neurology, Rikshospitalet University Hospital, Oslo, Norway
    Epilepsy Res 88:55-64. 2010

Detail Information

Publications3

  1. ncbi request reprint Neuro-ophthalmological findings in sarcoidosis
    Kjell Heuser
    Department of Neurology, Rikshospitalet, University of Oslo, Oslo, Norway
    Acta Ophthalmol Scand 82:723-9. 2004
    ..The presence of ophthalmological and neuro-ophthalmological findings may lead to diagnosis of the disease and the initiation of adequate treatment...
  2. ncbi request reprint Microvascular decompression for hemifacial spasm: postoperative neurologic follow-up and evaluation of life quality
    K Heuser
    Division for Clinical Neuroscience, Department of Neurology, Rikshospitalet Radiumhospitalet, University of Oslo, Oslo, Norway
    Eur J Neurol 14:335-40. 2007
    ..Median age of the patients with late effect (62.6 years) was significantly higher than in those with early effect (52.7 years)...
  3. doi request reprint Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy
    Kjell Heuser
    Department of Neurology, Rikshospitalet University Hospital, Oslo, Norway
    Epilepsy Res 88:55-64. 2010
    ..The current study was designed to identify variants of the AQP4 and KCNJ10 genes associated with TLE and subgroups of this condition...