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Items: 1 to 20 of 169

1.

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions.

Cairns NJ, Neumann M, Bigio EH, Holm IE, Troost D, Hatanpaa KJ, Foong C, White CL 3rd, Schneider JA, Kretzschmar HA, Carter D, Taylor-Reinwald L, Paulsmeyer K, Strider J, Gitcho M, Goate AM, Morris JC, Mishra M, Kwong LK, Stieber A, Xu Y, Forman MS, Trojanowski JQ, Lee VM, Mackenzie IR.

Am J Pathol. 2007 Jul;171(1):227-40.

2.

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration.

Cairns NJ, Bigio EH, Mackenzie IR, Neumann M, Lee VM, Hatanpaa KJ, White CL 3rd, Schneider JA, Grinberg LT, Halliday G, Duyckaerts C, Lowe JS, Holm IE, Tolnay M, Okamoto K, Yokoo H, Murayama S, Woulfe J, Munoz DG, Dickson DW, Ince PG, Trojanowski JQ, Mann DM; Consortium for Frontotemporal Lobar Degeneration.

Acta Neuropathol. 2007 Jul;114(1):5-22. Epub 2007 Jun 20.

3.

Frontotemporal dementias: update on recent developments in molecular genetics and neuropathology.

Liscić RM.

Arh Hig Rada Toksikol. 2009 Mar;60(1):117-22. doi: 10.2478/10004-1254-60-2009-1921. Review.

PMID:
19329383
4.

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.

Seelaar H, Schelhaas HJ, Azmani A, Küsters B, Rosso S, Majoor-Krakauer D, de Rijk MC, Rizzu P, ten Brummelhuis M, van Doorn PA, Kamphorst W, Willemsen R, van Swieten JC.

Brain. 2007 May;130(Pt 5):1375-85. Epub 2007 Mar 14.

PMID:
17360763
5.

ALS and FTLD: two faces of TDP-43 proteinopathy.

Liscic RM, Grinberg LT, Zidar J, Gitcho MA, Cairns NJ.

Eur J Neurol. 2008 Aug;15(8):772-80. doi: 10.1111/j.1468-1331.2008.02195.x. Review.

6.

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

Luty AA, Kwok JB, Thompson EM, Blumbergs P, Brooks WS, Loy CT, Dobson-Stone C, Panegyres PK, Hecker J, Nicholson GA, Halliday GM, Schofield PR.

BMC Neurol. 2008 Aug 29;8:32. doi: 10.1186/1471-2377-8-32.

7.

Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72.

Murray ME, DeJesus-Hernandez M, Rutherford NJ, Baker M, Duara R, Graff-Radford NR, Wszolek ZK, Ferman TJ, Josephs KA, Boylan KB, Rademakers R, Dickson DW.

Acta Neuropathol. 2011 Dec;122(6):673-90. doi: 10.1007/s00401-011-0907-y. Epub 2011 Nov 15.

8.

[TDP-43 proteinopathies: ALS and frontotemporal dementias].

Prudlo J.

Fortschr Neurol Psychiatr. 2009 Aug;77 Suppl 1:S25-7. doi: 10.1055/s-0028-1109602. Epub 2009 Aug 14. German.

PMID:
19685386
9.

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions.

Mackenzie IR, Foti D, Woulfe J, Hurwitz TA.

Brain. 2008 May;131(Pt 5):1282-93. doi: 10.1093/brain/awn061. Epub 2008 Mar 24.

PMID:
18362096
10.

Fine structural analysis of the neuronal inclusions of frontotemporal lobar degeneration with TDP-43 proteinopathy.

Thorpe JR, Tang H, Atherton J, Cairns NJ.

J Neural Transm (Vienna). 2008 Dec;115(12):1661-71. doi: 10.1007/s00702-008-0137-1. Epub 2008 Oct 31.

11.

TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.

Neumann M, Mackenzie IR, Cairns NJ, Boyer PJ, Markesbery WR, Smith CD, Taylor JP, Kretzschmar HA, Kimonis VE, Forman MS.

J Neuropathol Exp Neurol. 2007 Feb;66(2):152-7.

PMID:
17279000
12.

White matter lesions in the brain with frontotemporal lobar degeneration with motor neuron disease: TDP-43-immunopositive inclusions co-localize with p62, but not ubiquitin.

Hiji M, Takahashi T, Fukuba H, Yamashita H, Kohriyama T, Matsumoto M.

Acta Neuropathol. 2008 Aug;116(2):183-91. doi: 10.1007/s00401-008-0402-2. Epub 2008 Jun 27.

PMID:
18584184
13.

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

Mackenzie IR, Feldman H.

Dement Geriatr Cogn Disord. 2004;17(4):333-6.

PMID:
15178948
14.

[Yuasa-Mitsuyama disease].

Mitsuyama Y.

Brain Nerve. 2011 Feb;63(2):109-18. Review. Japanese.

PMID:
21301035
15.

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies.

Neumann M, Kwong LK, Lee EB, Kremmer E, Flatley A, Xu Y, Forman MS, Troost D, Kretzschmar HA, Trojanowski JQ, Lee VM.

Acta Neuropathol. 2009 Feb;117(2):137-49. doi: 10.1007/s00401-008-0477-9. Epub 2009 Jan 6.

16.

[FTLD/ALS as TDP-43 proteinopathies].

Ishihara T, Ariizumi Y, Shiga A, Yokoseki A, Sato T, Toyoshima Y, Kakita A, Takahashi H, Nishizawa M, Onodera O.

Rinsho Shinkeigaku. 2010 Nov;50(11):1022-4. Review. Japanese.

PMID:
21921552
17.

Gene expression analysis of frontotemporal lobar degeneration of the motor neuron disease type with ubiquitinated inclusions.

Mishra M, Paunesku T, Woloschak GE, Siddique T, Zhu LJ, Lin S, Greco K, Bigio EH.

Acta Neuropathol. 2007 Jul;114(1):81-94. Epub 2007 Jun 14.

PMID:
17569064
18.

Clinical entity of frontotemporal dementia with motor neuron disease.

Mitsuyama Y, Inoue T.

Neuropathology. 2009 Dec;29(6):649-54. doi: 10.1111/j.1440-1789.2009.01059.x. Epub 2009 Sep 22. Review.

PMID:
19780984
19.

An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.

Troakes C, Maekawa S, Wijesekera L, Rogelj B, Siklós L, Bell C, Smith B, Newhouse S, Vance C, Johnson L, Hortobágyi T, Shatunov A, Al-Chalabi A, Leigh N, Shaw CE, King A, Al-Sarraj S.

Neuropathology. 2012 Oct;32(5):505-14. doi: 10.1111/j.1440-1789.2011.01286.x. Epub 2011 Dec 19.

PMID:
22181065
20.

[Frontotemporal dementia (FTD) and genetic mutations including progranulin gene].

Arai T, Hasegawa M, Nishihara M, Nonaka T, Kametani F, Yoshida M, Hashizume Y, Beach TG, Morita M, Nakano I, Oda T, Tsuchiya K, Akiyama H.

Rinsho Shinkeigaku. 2008 Nov;48(11):990-3. Review. Japanese.

PMID:
19198141

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