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There are 11053 results for: content related to: Characteristics of frontotemporal dementia patients with a Progranulin mutation

  1. Molecular Genetics of Frontotemporal Dementia

    Standard Article


    Raffaele Ferrari, Avinash Thumma and Parastoo Momeni

    Published Online : 15 MAY 2013, DOI: 10.1002/9780470015902.a0024457

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    Progranulin: normal function and role in neurodegeneration

    Journal of Neurochemistry

    Volume 104, Issue 2, January 2008, Pages: 287–297, Jason L. Eriksen and Ian R. A. Mackenzie

    Article first published online : 15 SEP 2007, DOI: 10.1111/j.1471-4159.2007.04968.x

  3. Mouse models of frontotemporal dementia

    Annals of Neurology

    Volume 72, Issue 6, December 2012, Pages: 837–849, Erik D. Roberson

    Article first published online : 31 DEC 2012, DOI: 10.1002/ana.23722

  4. Frontotemporal dementia and related disorders: Deciphering the enigma

    Annals of Neurology

    Volume 64, Issue 1, July 2008, Pages: 4–14, Keith A. Josephs

    Article first published online : 30 JUL 2008, DOI: 10.1002/ana.21426

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    Frontotemporal Lobar Degeneration: Current Concepts in the Light of Recent Advances

    Brain Pathology

    Volume 17, Issue 1, January 2007, Pages: 104–114, Samir Kumar-Singh and Christine Van Broeckhoven

    Article first published online : 26 FEB 2007, DOI: 10.1111/j.1750-3639.2007.00055.x

  6. Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases

    Movement Disorders

    Volume 23, Issue 9, 15 July 2008, Pages: 1269–1273, Rita Joao Guerreiro, Isabel Santana, Jose Miguel Bras, Tamas Revesz, Olinda Rebelo, Maria Helena Ribeiro, Beatriz Santiago, Catarina Resende Oliveira, Andrew Singleton and John Hardy

    Article first published online : 7 MAY 2008, DOI: 10.1002/mds.22078

  7. Frontotemporal dementia: a bridge between dementia and neuromuscular disease

    Annals of the New York Academy of Sciences

    Volume 1338, Issue 1, March 2015, Pages: 71–93, Adeline S.L. Ng, Rosa Rademakers and Bruce L. Miller

    Article first published online : 30 DEC 2014, DOI: 10.1111/nyas.12638

  8. Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration

    European Journal of Neurology

    Volume 16, Issue 1, January 2009, Pages: 27–30, J. Krüger, A.-L. Kaivorinne, B. Udd, K. Majamaa and A. M. Remes

    Article first published online : 25 NOV 2008, DOI: 10.1111/j.1468-1331.2008.02272.x

  9. Regional Cerebral Blood Flow Single Photon Emission Computed Tomography for detection of Frontotemporal dementia in people with suspected dementia

    Diagnostic Test Accuracy Review

    The Cochrane Library

    Hilary A Archer, Nadja Smailagic, Christeena John, Robin B Holmes, Yemisi Takwoingi, Elizabeth J Coulthard and Sarah Cullum

    Published Online : 23 JUN 2015, DOI: 10.1002/14651858.CD010896.pub2

  10. Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images

    European Journal of Neurology

    Volume 22, Issue 5, May 2015, Pages: 745–752, J. L. Whitwell, B. F. Boeve, S. D. Weigand, M. L. Senjem, J. L. Gunter, M. C. Baker, M. DeJesus-Hernandez, D. S. Knopman, Z. K. Wszolek, R. C. Petersen, R. Rademakers, C. R. Jack Jr and K. A. Josephs

    Article first published online : 12 FEB 2015, DOI: 10.1111/ene.12675

  11. Frontal Lobe Disorders: Frontotemporal Dementia (Pick Disease)

    Standard Article


    Maria Carmela Tartaglia and Bruce Miller

    Published Online : 15 SEP 2009, DOI: 10.1002/9780470015902.a0021409

  12. Frontotemporal dementia linked to chromosome 3 (FTD-3) – current concepts and the detection of a previously unknown branch of the Danish FTD-3 family

    European Journal of Neurology

    Volume 15, Issue 7, July 2008, Pages: 667–670, S. G. Lindquist, H. Brændgaard, K. Svenstrup, A. M. Isaacs, J. E. Nielsen and on behalf of the FReJA Consortium

    Article first published online : 15 MAY 2008, DOI: 10.1111/j.1468-1331.2008.02144.x

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    Charting Frontotemporal Dementia: From Genes to Networks

    Journal of Neuroimaging

    Volume 26, Issue 1, January/February 2016, Pages: 16–27, Massimo Filippi, Federica Agosta and Pilar M. Ferraro

    Article first published online : 29 NOV 2015, DOI: 10.1111/jon.12316

  14. Bad neighbors cause dementia; a second 17q21-linked gene responsible for frontotemporal dementia

    Clinical Genetics

    Volume 70, Issue 5, November 2006, Pages: 385–387, SJ Neal and BR Leavitt

    Article first published online : 21 SEP 2006, DOI: 10.1111/j.1399-0004.2006.00699_3.x

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    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Article first published online : 19 JUN 2012, DOI: 10.1002/mds.25051

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    Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations

    Neuropathology and Applied Neurobiology

    Volume 41, Issue 7, December 2015, Pages: 858–881, Tammaryn Lashley, Jonathan D. Rohrer, Simon Mead and Tamas Revesz

    Article first published online : 6 JUL 2015, DOI: 10.1111/nan.12250

  17. Genetics of dementia: Update and guidelines for the clinician

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 6, September 2012, Pages: 628–643, Petra E. Cohn-Hokke, Mariet W. Elting, Yolande A.L. Pijnenburg and John C. van Swieten

    Article first published online : 19 JUL 2012, DOI: 10.1002/ajmg.b.32080

  18. Genetic testing in familial AD and FTD: Mutation and phenotype spectrum in a Danish cohort

    Clinical Genetics

    Volume 76, Issue 2, August 2009, Pages: 205–209, SG Lindquist, M Schwartz, M Batbayli, G Waldemar and JE Nielsen

    Article first published online : 29 JUL 2009, DOI: 10.1111/j.1399-0004.2009.01191.x

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    The granulin gene family: from cancer to dementia


    Volume 31, Issue 11, November 2009, Pages: 1245–1254, Andrew Bateman and Hugh P. J. Bennett

    Article first published online : 30 SEP 2009, DOI: 10.1002/bies.200900086

  20. HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

    Annals of Neurology

    Volume 60, Issue 3, September 2006, Pages: 314–322, Odity Mukherjee, Pau Pastor, Nigel J. Cairns, Sumi Chakraverty, John S. K. Kauwe, Shantia Shears, Maria I. Behrens, John Budde, Anthony L. Hinrichs, Joanne Norton, Denise Levitch, Lisa Taylor-Reinwald, Michael Gitcho, P.-H. Tu, Lea Tenenholz Grinberg, Rajka M. Liscic, Javier Armendariz, John C. Morris and Alison M. Goate

    Article first published online : 18 SEP 2006, DOI: 10.1002/ana.20963