Search Results - "Rosso, Sonia"

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    Survival in progressive supranuclear palsy and frontotemporal dementia by Chiu, Wang Zheng, Kaat, L D, Seelaar, Harro, Rosso, Sonia M, Boon, Agnita JW, Kamphorst, Wouter, van Swieten, John C

    “…ObjectiveTo compare survival and to identify prognostic predictors for progressive supranuclear palsy and frontotemporal dementia.BackgroundProgressive…”
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    Journal Article
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    Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21–22 by Rosso, Sonia M., Kamphorst, Wouter, de Graaf, Bianca, Willemsen, Rob, Ravid, Rivka, Niermeijer, Martinus F., Spillantini, Maria Grazia, Heutink, Peter, van Swieten, John C.

    Published in Brain (London, England : 1878) (01-10-2001)
    “…Hereditary frontotemporal dementia (FTD) is an autosomal dominant neurodegenerative disorder that is associated with mutations in the tau gene and with the…”
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    Frontotemporal dementia: change of familial caregiver burden and partner relation in a Dutch cohort of 63 patients by Riedijk, Samantha, Duivenvoorden, Hugo, Rosso, Sonia, Van Swieten, John, Niermeijer, Martinus, Tibben, Aad

    Published in Dementia and geriatric cognitive disorders (01-01-2008)
    “…The current study examined the change of caregiver burden and the development of the quality of the partner relation in frontotemporal dementia (FTD). During a…”
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    Journal Article
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    CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia by Rizzu, Patrizia, van Mil, Saskia E., Anar, Burcu, Rosso, Sonia M., Kaat, Laura Donker, Heutink, Peter, van Swieten, John C.

    “…Mutations in the CHMP2B gene have been recently identified in a large Danish pedigree with autosomal dominant frontotemporal dementia (FTD) linked to…”
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    A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease by Rosso, Sonia M., Van Herpen, Esther, Deelen, Wout, Kamphorst, Wouter, Severijnen, Lies-Anne, Willemsen, Rob, Ravid, Rivka, Niermeijer, Martinus F., Dooijes, Dennis, Smith, Michael J., Goedert, Michel, Heutink, Peter, Van Swieten, John C.

    Published in Annals of neurology (01-03-2002)
    “…Mutations in the tau gene cause familial frontotemporal dementia and parkinsonism linked to chromosome 17. In this article, we describe a novel missense…”
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    New developments in frontotemporal dementia and parkinsonism linked to chromosome 17 by Rosso, Sonia M, van Swieten, John C

    Published in Current opinion in neurology (01-08-2002)
    “…The identification of tau mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) has revealed invaluable information regarding…”
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    Journal Article
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    Complex compulsive behaviour in the temporal variant of frontotemporal dementia by ROSSO, Sonia M, ROKS, Gerwin, STEVENS, Martijn, DE KONING, Inge, TANGHE, Herve L. J, KAMPHORST, Wouter, RAVID, Rivka, NIERMEIJER, Martinus F, VAN SWIETEN, John C

    Published in Journal of neurology (01-11-2001)
    “…As metabolic and structural changes in frontotemporal-subcortical pathways have been reported in patients with obsessive-compulsive disorders, we investigated…”
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    Journal Article
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    Epidemiological aspects of frontotemporal dementia by van Swieten, John C., Rosso, Sonia M.

    Published in Handbook of Clinical Neurology (2008)
    “…This chapter explains that frontotemporal dementia (FTD) is a neurodegenerative disorder, characterized by progressive behavioral change and a disturbance of…”
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    Book Chapter Journal Article
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    Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17 by van Swieten, John C, Rosso, Sonia M, van Herpen, Esther, Kamphorst, Wouter, Ravid, Rivka, Heutink, Peter

    Published in Dementia and geriatric cognitive disorders (01-01-2004)
    “…Hereditary frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) caused by mutations in the tau gene shows a wide range in age at onset,…”
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    Journal Article
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    Progranulin mutations in Dutch familial frontotemporal lobar degeneration by BRONNER, Iraad F, RIZZU, Patrizia, SEELAAR, Harro, VAN MIL, Saskia E, ANARL, Burcu, AZMANI, Asma, DONKER KAAT, Laura, ROSSO, Sonia, HEUTINK, Peter, VAN SWIETEN, John C

    Published in European journal of human genetics : EJHG (01-03-2007)
    “…Mutations in the progranulin (PGRN) gene have recently been identified in frontotemporal lobar degeneration with ubiquitin inclusions linked to chromosome…”
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    Journal Article
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    Progranulin mutations in Dutch familial frontotemporal lobar degeneration by Bronner, Iraad F, Rizzu, Patrizia, Seelaar, Harro, Van Mil, Saskia E, Anar, Burcu, Azmani, Asma, Kaat, Laura Donker, Rosso, Sonia, Heutink, Peter, Van Swieten, John C

    Published in European journal of human genetics : EJHG (01-03-2007)
    “…Mutations in the progranulin (PGRN) gene have recently been identified in frontotemporal lobar degeneration with ubiquitin inclusions linked to chromosome…”
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    Journal Article
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