Search Results - "van Swieten, J. C."

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  1. 1

    Distinct genetic forms of frontotemporal dementia by SEELAAR, H, KAMPHORST, W, DOOIJES, D, ROZEMULLER, J. M, BRONNER, I. F, RIZZU, P, VAN SWIETEN, J. C, ROSSO, S. M, AZMANI, A, MASDJEDI, R, DE KONING, I, MAAT-KIEVIT, J. A, ANAR, B, DONKER KAAT, L, BREEDVELD, G. J

    Published in Neurology (14-10-2008)
    “…Frontotemporal dementia (FTD) is the second most common type of presenile dementia and can be distinguished into various clinical variants. The identification…”
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    Journal Article
  2. 2

    CSF biomarkers in frontotemporal lobar degeneration with known pathology by BIAN, H, VAN SWIETEN, J. C, TROJANOWSKI, J, LEE, V. M.-Y, GROSSMAN, M, LEIGHT, S, MASSIMO, L, WOOD, E, FORMAN, M, MOORE, P, DE KONING, I, CLARK, C. M, ROSSO, S

    Published in Neurology (06-05-2008)
    “…To evaluate the diagnostic value of CSF biomarkers in patients with known pathology due to frontotemporal lobar degeneration (FTLD). It is important to…”
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    Journal Article
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    Frontal presentation in progressive supranuclear palsy by DONKER KAAT, L, BOON, A. J. W, KAMPHORST, W, RAVID, R, DUIVENVOORDEN, H. J, VAN SWIETEN, J. C

    Published in Neurology (21-08-2007)
    “…Progressive supranuclear palsy (PSP) is a progressive hypokinetic rigid disorder with supranuclear gaze palsy and frequent falls. Although clinical consensus…”
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    Journal Article
  5. 5

    Familial aggregation of parkinsonism in progressive supranuclear palsy by KAAT, L. Donker, BOON, A. J. W, AZMANI, A, KAMPHORST, W, BRETELER, M. M. B, ANAR, B, HEUTINK, P, VAN SWIETEN, J. C

    Published in Neurology (14-07-2009)
    “…Progressive supranuclear palsy (PSP) is a progressive neurodegenerative disorder characterized by aggregates of the microtubule-associated protein tau (MAPT)…”
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    Diagnosis and management of early- and late-onset cerebellar ataxia by Brusse, E, Maat-Kievit, JA, Van Swieten, JC

    Published in Clinical genetics (01-01-2007)
    “…Cerebellar ataxias represent a heterogeneous group of neurodegenerative disorders. Two main categories are distinguished: hereditary and sporadic ataxias…”
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  8. 8

    Diet and risk of dementia: Does fat matter? The Rotterdam Study by ENGELHART, M. J, GEERLINGS, M. I, RUITENBERG, A, VAN SWIETEN, J. C, HOFMAN, A, WITTEMAN, J. C. M, BRETELER, M. M. B

    Published in Neurology (24-12-2002)
    “…To examine whether high intake of total fat, saturated fatty acids (saturated fat), trans fatty acids (trans fat), and cholesterol and low intake of…”
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    Journal Article
  9. 9

    Insulin-resistance and metabolic syndrome are related to executive function in women in a large family-based study by Schuur, M., Henneman, P., van Swieten, J. C., Zillikens, M. C., de Koning, I., Janssens, A. C. J. W., Witteman, J. C. M., Aulchenko, Y. S., Frants, R. R., Oostra, B. A., van Dijk, K. Willems, van Duijn, C. M.

    Published in European journal of epidemiology (01-08-2010)
    “…While type 2 diabetes is well-known to be associated with poorer cognitive performance, few studies have reported on the association of metabolic syndrome…”
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  10. 10

    Review: Fluid biomarkers for frontotemporal dementias by Zetterberg, H., van Swieten, J. C., Boxer, A. L., Rohrer, J. D.

    Published in Neuropathology and applied neurobiology (01-02-2019)
    “…Frontotemporal dementias (FTDs) are clinically, genetically and pathologically heterogeneous neurodegenerative disorders that affect the frontal and anterior…”
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    Journal Article
  11. 11

    Medical and environmental risk factors for sporadic frontotemporal dementia: a retrospective case–control study by Rosso, S M, Landweer, E-J, Houterman, M, Donker Kaat, L, van Duijn, C M, van Swieten, J C

    “…A retrospective case-control study was carried out on 80 patients with sporadic frontotemporal dementia and 124 age, sex, and surrogate informant matched…”
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  12. 12

    PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36 by van Duijn, C.M., Dekker, M.C.J., Bonifati, V., Galjaard, R.J., Houwing-Duistermaat, J.J., Snijders, P.J.L.M., Testers, L., Breedveld, G.J., Horstink, M., Sandkuijl, L.A., van Swieten, J.C., Oostra, B.A., Heutink, P.

    Published in American journal of human genetics (01-09-2001)
    “…Although the role of genetic factors in the origin of Parkinson disease has long been disputed, several genes involved in autosomal dominant and recessive…”
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  13. 13

    Caregiver burden, health-related quality of life and coping in dementia caregivers: a comparison of frontotemporal dementia and Alzheimer's disease by Riedijk, S R, De Vugt, M E, Duivenvoorden, H J, Niermeijer, M F, Van Swieten, J C, Verhey, F R J, Tibben, A

    Published in Dementia and geriatric cognitive disorders (01-01-2006)
    “…Frontotemporal dementia (FTD) is the second most prevalent dementia after Alzheimer's disease (AD). We compared 29 FTD and 90 AD caregivers with respect to…”
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  14. 14

    Amyloid β(1-42) and phosphorylated tau in CSF as markers for early-onset Alzheimer disease by SCHOONENBOOM, N. S. M, PIJNENBURG, Y. A. L, MULDER, C, ROSSO, S. M, VAN ELK, E.-J, VAN KAMP, G. J, VAN SWIETEN, J. C, SCHELTENS, Ph

    Published in Neurology (11-05-2004)
    “…To determine the diagnostic value of CSF amyloid beta(1-42) (Abeta42), CSF total tau, and CSF tau phosphorylated at threonine-181 (Ptau-181) in early-onset…”
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    Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology by Bronner, I. F., ter Meulen, B. C., Azmani, A., Severijnen, L. A., Willemsen, R., Kamphorst, W., Ravid, R., Heutink, P., van Swieten, J. C.

    Published in Brain (London, England : 1878) (01-11-2005)
    “…Frontotemporal dementia and parkinsonism linked to chromosome 17 have been associated with mutations in the microtubule associated protein tau (MAPT or tau)…”
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  16. 16

    Brain perfusion patterns in familial frontotemporal lobar degeneration by SEELAAR, H, PAPMA, J. M, GARRAUX, G, DE KONING, I, REIJS, A. E, VALKEMA, R, ROZEMULLER, A. J. M, SALMON, E, VAN SWIETEN, J. C

    Published in Neurology (26-07-2011)
    “…Frontotemporal lobar degeneration (FTLD) is a clinically, genetically, and pathologically heterogeneous disorder. The aim of this study was to compare clinical…”
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    Journal Article Web Resource
  17. 17

    Tau Pathology in Two Dutch Families with Mutations in the Microtubule-Binding Region of Tau by Spillantini, M.G., Crowther, R.A., Kamphorst, W., Heutink, P., van Swieten, J.C.

    Published in The American journal of pathology (01-11-1998)
    “…Different mutations in the microtubule-associated tau protein gene have recently been identified in several families with hereditary frontotemporal dementia…”
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    Journal Article Conference Proceeding
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    Cognitive profiles discriminate between genetic variants of behavioral frontotemporal dementia by Poos, J. M., Jiskoot, L. C., Leijdesdorff, S. M. J., Seelaar, H., Panman, J. L., van der Ende, E. L., Mol, M. O., Meeter, L. H. H., Pijnenburg, Y. A. L., Donker Kaat, L., de Jong, F. J., van Swieten, J. C., Papma, J. M., van den Berg, E.

    Published in Journal of neurology (01-06-2020)
    “…Introduction Trials to test disease-modifying treatments for frontotemporal dementia are eagerly awaited and sensitive instruments to assess potential…”
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    Recent advances in progressive supranuclear palsy: a review by Kaat, D L, Chiu, W Z, Boon, A J W, van Swieten, J C

    Published in Current Alzheimer research (01-05-2011)
    “…Progressive Supranuclear Palsy has been used over decades as a term denoting an uniform disorder with progressive parkinsonism with early falls, vertical…”
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  20. 20

    Phenotypic variation in hereditary frontotemporal dementia with tau mutations by Van Swieten, J. C., Stevens, M., Rosso, S. M., Rizzu, P., Joosse, M., De Koning, I., Kamphorst, W., Ravid, R., Spillantini, M. G., Niermeijer, M. F., Heutink, P.

    Published in Annals of neurology (01-10-1999)
    “…Several mutations in the tau gene have been found in families with hereditary frontotemporal dementia and parkinsonism linked to chromosome 17q21‐22 (FTDP‐17)…”
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    Journal Article