Agnes A Luty

Summary

Affiliation: Prince of Wales Medical Research Institute
Country: Australia

Publications

  1. pmc Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
    Agnes A Luty
    Prince of Wales Medical Research Institute, Sydney, NSW, Australia
    BMC Neurol 8:32. 2008
  2. pmc Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis
    Carol Dobson-Stone
    Neuroscience Research Australia, Barker St, Randwick, Sydney, NSW 2031, Australia
    Acta Neuropathol 125:523-33. 2013
  3. doi Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease
    Agnes A Luty
    Neuroscience Research Australia, Randwick, Sydney, New South Wales, Australia
    Ann Neurol 68:639-49. 2010

Collaborators

Detail Information

Publications3

  1. pmc Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
    Agnes A Luty
    Prince of Wales Medical Research Institute, Sydney, NSW, Australia
    BMC Neurol 8:32. 2008
    ..The objective in this study is to identify the genetic locus in a multi-generational Australian family with FTLD-MND...
  2. pmc Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis
    Carol Dobson-Stone
    Neuroscience Research Australia, Barker St, Randwick, Sydney, NSW 2031, Australia
    Acta Neuropathol 125:523-33. 2013
    ..This region overlaps with a separate locus on 16q12.1-q12.2 reported in an independent ALS family, indicating that this region may harbour a second major locus for FTD-ALS...
  3. doi Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease
    Agnes A Luty
    Neuroscience Research Australia, Randwick, Sydney, New South Wales, Australia
    Ann Neurol 68:639-49. 2010
    ..Our objective was to identify the causative gene in an FTLD-MND pedigree with no mutations in known dementia genes...