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Journal Abstract Search

226 related items for PubMed ID: 10683298

  • 1. Search for a mutation in the tau gene in a Swiss family with frontotemporal dementia.
    Savioz A, Kövari E, Anastasiu R, Rossier C, Saini K, Bouras C, Leuba G.
    Exp Neurol; 2000 Jan; 161(1):330-5. PubMed ID: 10683298
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  • 3. Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17.
    Kobayashi T, Mori H, Okuma Y, Dickson DW, Cookson N, Tsuboi Y, Motoi Y, Tanaka R, Miyashita N, Anno M, Narabayashi H, Mizuno Y.
    J Neurol; 2002 Jun; 249(6):669-75. PubMed ID: 12111297
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  • 9. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.
    Zarranz JJ, Ferrer I, Lezcano E, Forcadas MI, Eizaguirre B, Atarés B, Puig B, Gómez-Esteban JC, Fernández-Maiztegui C, Rouco I, Pérez-Concha T, Fernández M, Rodríguez O, Rodríguez-Martínez AB, de Pancorbo MM, Pastor P, Pérez-Tur J.
    Neurology; 2005 May 10; 64(9):1578-85. PubMed ID: 15883319
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  • 10. Frontotemporal dementia--a brief review.
    Sjögren M, Andersen C.
    Mech Ageing Dev; 2006 Feb 10; 127(2):180-7. PubMed ID: 16330083
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  • 13. Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.
    Ingelsson M, Ramasamy K, Russ C, Freeman SH, Orne J, Raju S, Matsui T, Growdon JH, Frosch MP, Ghetti B, Brown RH, Irizarry MC, Hyman BT.
    Acta Neuropathol; 2007 Nov 10; 114(5):471-9. PubMed ID: 17721707
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  • 14. Phenotypic heterogeneity within a new family with the MAPT p301s mutation.
    Yasuda M, Nakamura Y, Kawamata T, Kaneyuki H, Maeda K, Komure O.
    Ann Neurol; 2005 Dec 10; 58(6):920-8. PubMed ID: 16240366
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  • 20. [Genetics of frontotemporal dementia and alterations of the tau gene].
    Oliva R.
    Neurologia; 2000 Jan 10; 15 Suppl 1():33-7. PubMed ID: 10723173
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