Sonia M Rosso

Summary

Affiliation: Erasmus MC
Country: The Netherlands

Publications

  1. ncbi request reprint Total tau and phosphorylated tau 181 levels in the cerebrospinal fluid of patients with frontotemporal dementia due to P301L and G272V tau mutations
    Sonia M Rosso
    Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
    Arch Neurol 60:1209-13. 2003
  2. pmc Medical and environmental risk factors for sporadic frontotemporal dementia: a retrospective case-control study
    S M Rosso
    Departments of Neurology, Erasmus Medical Centre Rotterdam, Rotterdam, Netherlands
    J Neurol Neurosurg Psychiatry 74:1574-6. 2003
  3. ncbi request reprint Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R
    Esther van Herpen
    Department of Clinical Genetics, Erasmus Medical Center, Dr Molewaterplein 40, 3015 GD Rotterdam, The Netherlands
    Ann Neurol 54:573-81. 2003
  4. ncbi request reprint Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17
    John C van Swieten
    Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
    Dement Geriatr Cogn Disord 17:261-4. 2004
  5. ncbi request reprint Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study
    Sonia M Rosso
    Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
    Brain 126:2016-22. 2003
  6. ncbi request reprint A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease
    Sonia M Rosso
    Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
    Ann Neurol 51:373-6. 2002
  7. doi request reprint Survival in progressive supranuclear palsy and frontotemporal dementia
    Wang Zheng Chiu
    Department of Neurology, Erasmus University Medical Centre Rotterdam, Room Hs 611, s Gravendijkwal 230, 3015 CE Rotterdam, The Netherlands
    J Neurol Neurosurg Psychiatry 81:441-5. 2010
  8. ncbi request reprint New developments in frontotemporal dementia and parkinsonism linked to chromosome 17
    Sonia M Rosso
    Department of Neurology, Erasmus Medical Centre, University Hospital Dijkzigt, Dr Molewaterplein 40, 3015 GD Rotterdam, The Netherlands
    Curr Opin Neurol 15:423-8. 2002
  9. ncbi request reprint CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia
    Patrizia Rizzu
    Department of Human Genetics, Section Medical Genomics, VU University, Amsterdam, The Netherlands
    Am J Med Genet B Neuropsychiatr Genet 141:944-6. 2006

Collaborators

Detail Information

Publications9

  1. ncbi request reprint Total tau and phosphorylated tau 181 levels in the cerebrospinal fluid of patients with frontotemporal dementia due to P301L and G272V tau mutations
    Sonia M Rosso
    Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
    Arch Neurol 60:1209-13. 2003
    ..Mutations in the tau gene have been found in the familial form of FTD, linked to chromosome 17q21-22, showing a spectrum of tauopathy...
  2. pmc Medical and environmental risk factors for sporadic frontotemporal dementia: a retrospective case-control study
    S M Rosso
    Departments of Neurology, Erasmus Medical Centre Rotterdam, Rotterdam, Netherlands
    J Neurol Neurosurg Psychiatry 74:1574-6. 2003
    ..9 to 7.9), which was not statistically significant (p = 0.09) owing to limited power. As altered thyroid hormone status has been observed before in frontotemporal dementia, future studies will be important to confirm this observation...
  3. ncbi request reprint Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R
    Esther van Herpen
    Department of Clinical Genetics, Erasmus Medical Center, Dr Molewaterplein 40, 3015 GD Rotterdam, The Netherlands
    Ann Neurol 54:573-81. 2003
    ..All six tau isoforms were present in soluble brain tau. Recombinant tau proteins with the L315R mutation showed a reduced ability to promote microtubule assembly...
  4. ncbi request reprint Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17
    John C van Swieten
    Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
    Dement Geriatr Cogn Disord 17:261-4. 2004
    ..Future research should focus on the role of other genetic and environmental factors in this form of FTDP-17, whereas the responsible gene defect(s) has still to be identified for hereditary FTD without tau mutations...
  5. ncbi request reprint Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study
    Sonia M Rosso
    Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
    Brain 126:2016-22. 2003
    ..The finding of tau mutations in 32% of patients with a positive family history for dementia justifies mutation screening in FTD patients with a positive family history, while tau mutations in non-familiar cases are rare...
  6. ncbi request reprint A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease
    Sonia M Rosso
    Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands
    Ann Neurol 51:373-6. 2002
    ..Recombinant tau protein with the S320F mutation showed a greatly reduced ability to promote microtubule assembly...
  7. doi request reprint Survival in progressive supranuclear palsy and frontotemporal dementia
    Wang Zheng Chiu
    Department of Neurology, Erasmus University Medical Centre Rotterdam, Room Hs 611, s Gravendijkwal 230, 3015 CE Rotterdam, The Netherlands
    J Neurol Neurosurg Psychiatry 81:441-5. 2010
    ..To compare survival and to identify prognostic predictors for progressive supranuclear palsy and frontotemporal dementia...
  8. ncbi request reprint New developments in frontotemporal dementia and parkinsonism linked to chromosome 17
    Sonia M Rosso
    Department of Neurology, Erasmus Medical Centre, University Hospital Dijkzigt, Dr Molewaterplein 40, 3015 GD Rotterdam, The Netherlands
    Curr Opin Neurol 15:423-8. 2002
    ..Over the past year several new mutations have been identified, and experimental studies have provided further insight into the mechanism of neurodegeneration due to tau mutations and possible interactions with amyloid pathology...
  9. ncbi request reprint CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia
    Patrizia Rizzu
    Department of Human Genetics, Section Medical Genomics, VU University, Amsterdam, The Netherlands
    Am J Med Genet B Neuropsychiatr Genet 141:944-6. 2006
    ..Our results suggest that mutations in CHMP2B are a rare cause of FTD as compared to MAPT mutations...