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Items: 1 to 20 of 389

1.

Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease.

Mackenzie IR, Butland SL, Devon RS, Dwosh E, Feldman H, Lindholm C, Neal SJ, Ouellette BF, Leavitt BR.

BMC Neurol. 2006 Aug 31;6:32.

2.

Ubiquitin immunohistochemistry of frontotemporal lobar degeneration differentiates cases with and without motor neuron disease.

Katsuse O, Dickson DW.

Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19 Suppl 1:S37-43.

PMID:
16317257
3.

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

Mackenzie IR, Baker M, Pickering-Brown S, Hsiung GY, Lindholm C, Dwosh E, Gass J, Cannon A, Rademakers R, Hutton M, Feldman HH.

Brain. 2006 Nov;129(Pt 11):3081-90.

4.

Frontotemporal dementia with ubiquitinated cytoplasmic and intranuclear inclusions.

Woulfe J, Kertesz A, Munoz DG.

Acta Neuropathol. 2001 Jul;102(1):94-102.

PMID:
11547957
5.

CAG-encoded polyglutamine length polymorphism in the human genome.

Butland SL, Devon RS, Huang Y, Mead CL, Meynert AM, Neal SJ, Lee SS, Wilkinson A, Yang GS, Yuen MM, Hayden MR, Holt RA, Leavitt BR, Ouellette BF.

BMC Genomics. 2007 May 22;8:126.

6.

Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration.

Lladó A, Sánchez-Valle R, Rey MJ, Ezquerra M, Tolosa E, Ferrer I, Molinuevo JL; Catalan collaborative Study Group for FTLD.

J Neurol. 2008 Apr;255(4):488-94. doi: 10.1007/s00415-008-0565-8. Epub 2008 Mar 25.

PMID:
18357425
7.

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17.

Mackenzie IR, Baker M, West G, Woulfe J, Qadi N, Gass J, Cannon A, Adamson J, Feldman H, Lindholm C, Melquist S, Pettman R, Sadovnick AD, Dwosh E, Whiteheart SW, Hutton M, Pickering-Brown SM.

Brain. 2006 Apr;129(Pt 4):853-67. Epub 2006 Jan 9.

9.

Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis.

Bigio EH, Johnson NA, Rademaker AW, Fung BB, Mesulam MM, Siddique N, Dellefave L, Caliendo J, Freeman S, Siddique T.

J Neuropathol Exp Neurol. 2004 Aug;63(8):801-11.

10.

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation.

Shi J, Shaw CL, Du Plessis D, Richardson AM, Bailey KL, Julien C, Stopford C, Thompson J, Varma A, Craufurd D, Tian J, Pickering-Brown S, Neary D, Snowden JS, Mann DM.

Acta Neuropathol. 2005 Nov;110(5):501-12. Epub 2005 Oct 13.

PMID:
16222525
11.

Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases.

Mackenzie IR, Feldman H.

Acta Neuropathol. 2003 Jun;105(6):543-8. Epub 2003 Feb 15.

PMID:
12734660
12.

[Polyglutamine diseases: a pathologic view].

Yamada M.

Rinsho Shinkeigaku. 2003 Nov;43(11):903-5. Review. Japanese.

PMID:
15152499
13.

The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein.

Taniguchi S, McDonagh AM, Pickering-Brown SM, Umeda Y, Iwatsubo T, Hasegawa M, Mann DM.

Neuropathol Appl Neurobiol. 2004 Feb;30(1):1-18.

PMID:
14720172
14.

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

Fujigasaki H, Martin JJ, De Deyn PP, Camuzat A, Deffond D, Stevanin G, Dermaut B, Van Broeckhoven C, Dürr A, Brice A.

Brain. 2001 Oct;124(Pt 10):1939-47.

15.

Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions.

Kertesz A, Kawarai T, Rogaeva E, St George-Hyslop P, Poorkaj P, Bird TD, Munoz DG.

Neurology. 2000 Feb 22;54(4):818-27.

PMID:
10690970
16.

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

Rosso SM, Kamphorst W, de Graaf B, Willemsen R, Ravid R, Niermeijer MF, Spillantini MG, Heutink P, van Swieten JC.

Brain. 2001 Oct;124(Pt 10):1948-57.

17.

Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.

Ikeda Y, Daughters RS, Ranum LP.

Cerebellum. 2008;7(2):150-8. doi: 10.1007/s12311-008-0010-7.

PMID:
18418692
18.

The genetic and pathological classification of familial frontotemporal dementia.

Morris HR, Khan MN, Janssen JC, Brown JM, Perez-Tur J, Baker M, Ozansoy M, Hardy J, Hutton M, Wood NW, Lees AJ, Revesz T, Lantos P, Rossor MN.

Arch Neurol. 2001 Nov;58(11):1813-6.

PMID:
11708988
19.

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.

Arch Neurol. 2004 Feb;61(2):209-12.

PMID:
14967767
20.

FUS pathology in basophilic inclusion body disease.

Munoz DG, Neumann M, Kusaka H, Yokota O, Ishihara K, Terada S, Kuroda S, Mackenzie IR.

Acta Neuropathol. 2009 Nov;118(5):617-27. doi: 10.1007/s00401-009-0598-9. Epub 2009 Oct 15.

PMID:
19830439
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