R Myhre

Summary

Affiliation: Norwegian University of Science and Technology
Country: Norway

Publications

  1. pmc Genetic association study of synphilin-1 in idiopathic Parkinson's disease
    Ronny Myhre
    Department of Laboratory Medicine, Children s and Women s Health, Norwegian University of Science and Technology, Trondheim, Norway
    BMC Med Genet 9:19. 2008
  2. doi request reprint Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population
    R Myhre
    Department of Laboratory Medicine, Children s and Women s Health, Norwegian University of Science and Technology, Trondheim, Norway
    Acta Neurol Scand 118:320-7. 2008
  3. pmc Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism
    Ronny Myhre
    Department of Laboratory Medicine, Children s and Women s Health, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway
    BMC Neurol 8:47. 2008
  4. pmc PINK1 mutation heterozygosity and the risk of Parkinson's disease
    M Toft
    Department of Neuroscience, Norwegian University of Science and Technology NTNU, N 7489 Trondheim, Norway
    J Neurol Neurosurg Psychiatry 78:82-4. 2007
  5. doi request reprint The HLA-G 14bp gene polymorphism and decidual HLA-G 14bp gene expression in pre-eclamptic and normal pregnancies
    Ann Charlotte Iversen
    Department of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Women and Children s Centre, Okav Kyrres gt 11, Trondheim, Norway
    J Reprod Immunol 78:158-65. 2008
  6. ncbi request reprint Alpha-synuclein missense and multiplication mutations in autosomal dominant Parkinson's disease
    Andrew D Hope
    Laboratory of Neurogenetics, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA
    Neurosci Lett 367:97-100. 2004

Detail Information

Publications6

  1. pmc Genetic association study of synphilin-1 in idiopathic Parkinson's disease
    Ronny Myhre
    Department of Laboratory Medicine, Children s and Women s Health, Norwegian University of Science and Technology, Trondheim, Norway
    BMC Med Genet 9:19. 2008
    ..In the present study, we have investigated whether common variability in synphilin-1, including coding substitutions are genetically associated with disease pathogenesis...
  2. doi request reprint Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population
    R Myhre
    Department of Laboratory Medicine, Children s and Women s Health, Norwegian University of Science and Technology, Trondheim, Norway
    Acta Neurol Scand 118:320-7. 2008
    ..Our aim was to study SNCA gene markers in a closely matched Norwegian PD population to examine the genetic relationship between different polymorphisms associated with the disease...
  3. pmc Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism
    Ronny Myhre
    Department of Laboratory Medicine, Children s and Women s Health, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway
    BMC Neurol 8:47. 2008
    ....
  4. pmc PINK1 mutation heterozygosity and the risk of Parkinson's disease
    M Toft
    Department of Neuroscience, Norwegian University of Science and Technology NTNU, N 7489 Trondheim, Norway
    J Neurol Neurosurg Psychiatry 78:82-4. 2007
    ..Mutations in the PTEN-induced kinase 1 (PINK1) gene have been identified in recessively inherited and sporadic early-onset parkinsonism (EOP)...
  5. doi request reprint The HLA-G 14bp gene polymorphism and decidual HLA-G 14bp gene expression in pre-eclamptic and normal pregnancies
    Ann Charlotte Iversen
    Department of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Women and Children s Centre, Okav Kyrres gt 11, Trondheim, Norway
    J Reprod Immunol 78:158-65. 2008
    ..In conclusion, the fetal HLA-G 14bp genotype is reflected in the decidual HLA-G mRNA splice form profile, but does not appear to be associated with increased risk for development of PE...
  6. ncbi request reprint Alpha-synuclein missense and multiplication mutations in autosomal dominant Parkinson's disease
    Andrew D Hope
    Laboratory of Neurogenetics, Mayo Clinic Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA
    Neurosci Lett 367:97-100. 2004
    ..All samples were diploid with two normal copies of the SNCA locus. Hence, alpha-synuclein missense mutations and SNCA genomic multiplications remain a rare cause of disease...