Search Results - "Rosso, Sonia"
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Survival in progressive supranuclear palsy and frontotemporal dementia
Published in Journal of neurology, neurosurgery and psychiatry (01-04-2010)“…ObjectiveTo compare survival and to identify prognostic predictors for progressive supranuclear palsy and frontotemporal dementia.BackgroundProgressive…”
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Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population‐based study
Published in Brain (London, England : 1878) (01-09-2003)“…Since 1994, a population‐based study of frontotemporal dementia (FTD) in The Netherlands has aimed to ascertain all patients with FTD, and first prevalence…”
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Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21–22
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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Epidemiology and genetics of frontotemporal dementia/Pick's disease
Published in Annals of neurology (2003)Get full text
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Frontotemporal dementia: change of familial caregiver burden and partner relation in a Dutch cohort of 63 patients
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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CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05-12-2006)“…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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Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R
Published in Annals of neurology (01-11-2003)“…Mutations in the tau gene cause familial frontotemporal dementia and parkinsonism linked to chromosome 17. Here, we describe two Dutch families with familial…”
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A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease
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
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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10
Complex compulsive behaviour in the temporal variant of frontotemporal dementia
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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Epidemiological aspects of frontotemporal dementia
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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Frontotemporal dementia (FTD) patients living at home and their spousal caregivers compared with institutionalized FTD patients and their spousal caregivers: Which characteristics are associated with in-home care?
Published in Dementia (London, England) (01-02-2009)“…Patients with frontotemporal dementia (FTD) need complete care in the final stages of the disease. Some informal caregivers continue the in-home care whereas…”
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Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17
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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Total tau and phosphorylated tau 181 levels in the cerebrospinal fluid of patients with frontotemporal dementia due to P301L and G272V tau mutations
Published in Archives of neurology (Chicago) (01-09-2003)“…Frontotemporal dementia (FTD) is a pathologically heterogeneous group of presenile neurodegenerative disorders, with or without the deposition of…”
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TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations
Published in Brain (London, England : 1878) (01-05-2007)“…Frontotemporal dementia is accompanied by motor neuron disease (FTD + MND) in ∼10% of cases. There is accumulating evidence for a clinicopathological overlap…”
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Progranulin mutations in Dutch familial frontotemporal lobar degeneration
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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Progranulin mutations in Dutch familial frontotemporal lobar degeneration
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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P3-348 Familial occurrence of frontotemporal dementia without mutations in the tau gene
Published in Neurobiology of aging (01-07-2004)Get full text
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The recognition of a small group with exclusive mediotemporal pathology (pick D) within the spectrum of frontotemporal dementia
Published in Neurobiology of aging (01-05-2000)Get full text
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Coexistent tau and amyloid pathology in hereditary frontotemporal dementia with tau mutations
Published in Neurobiology of aging (01-05-2000)Get full text
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