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Items: 1 to 20 of 44

1.

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
2.

Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy.

Guinto JB, Ritson GP, Taylor JP, Forman MS.

Acta Neuropathol. 2007 Jul;114(1):55-61. Epub 2007 Apr 25. Review.

PMID:
17457594
3.

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.

Weihl CC, Pestronk A, Kimonis VE.

Neuromuscul Disord. 2009 May;19(5):308-15. doi: 10.1016/j.nmd.2009.01.009. Epub 2009 Apr 19. Review.

4.

Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update.

van der Zee J, Gijselinck I, Pirici D, Kumar-Singh S, Cruts M, Van Broeckhoven C.

Neurodegener Dis. 2007;4(2-3):227-35. Review.

PMID:
17596717
5.

The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.

Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, Nguyen C, Mukherjee J, Caiozzo V, Martin B, Watts GD, Vesa J, Smith C, Kimonis VE.

J Mol Neurosci. 2011 Nov;45(3):522-31. doi: 10.1007/s12031-011-9627-y. Epub 2011 Sep 3. Review.

PMID:
21892620
7.

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder.

Kimonis VE, Fulchiero E, Vesa J, Watts G.

Biochim Biophys Acta. 2008 Dec;1782(12):744-8. doi: 10.1016/j.bbadis.2008.09.003. Epub 2008 Sep 18. Review.

8.

[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
9.

Pathology and genetics of frontotemporal lobar degeneration: an update.

Tolnay M, Frank S.

Clin Neuropathol. 2007 Jul-Aug;26(4):143-56. Review.

PMID:
17702495
10.

A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.

Fanganiello RD, Kimonis VE, Côrte CC, Nitrini R, Passos-Bueno MR.

Braz J Med Biol Res. 2011 Apr;44(4):374-80. Epub 2011 Mar 11. Review.

11.

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.

12.

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.

13.

Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy.

Ju JS, Weihl CC.

Hum Mol Genet. 2010 Apr 15;19(R1):R38-45. doi: 10.1093/hmg/ddq157. Epub 2010 Apr 21. Review.

14.

The genetics of frontotemporal lobar degeneration.

Rademakers R, Hutton M.

Curr Neurol Neurosci Rep. 2007 Sep;7(5):434-42. Review.

PMID:
17764635
15.

TDP-43 and frontotemporal dementia.

Hu WT, Grossman M.

Curr Neurol Neurosci Rep. 2009 Sep;9(5):353-8. Review.

PMID:
19664364
16.

The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments.

Mackenzie IR, Rademakers R.

Neurogenetics. 2007 Nov;8(4):237-48. Epub 2007 Sep 6. Review.

PMID:
17805587
17.

[Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia].

Hayashi Y.

Rinsho Shinkeigaku. 2013;53(11):947-50. Review. Japanese.

PMID:
24291843
18.

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
19.

[Component of ubiquitin-positive inclusions in ALS].

Hasegawa M, Arai T.

Brain Nerve. 2007 Oct;59(10):1171-7. Review. Japanese.

PMID:
17969358
20.

[Pick's disease: clinicopathological features for antemortem diagnosis].

Yokota O, Tsuchiya K.

Rinsho Shinkeigaku. 2009 May;49(5):235-48. Review. Japanese.

PMID:
19594100

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