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Results: 1 to 20 of 129

Similar articles for PubMed (Select 24353332)

1.

In vivo signatures of nonfluent/agrammatic primary progressive aphasia caused by FTLD pathology.

Caso F, Mandelli ML, Henry M, Gesierich B, Bettcher BM, Ogar J, Filippi M, Comi G, Magnani G, Sidhu M, Trojanowski JQ, Huang EJ, Grinberg LT, Miller BL, Dronkers N, Seeley WW, Gorno-Tempini ML.

Neurology. 2014 Jan 21;82(3):239-47. doi: 10.1212/WNL.0000000000000031. Epub 2013 Dec 18.

2.

TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia.

Rohrer JD, Geser F, Zhou J, Gennatas ED, Sidhu M, Trojanowski JQ, Dearmond SJ, Miller BL, Seeley WW.

Neurology. 2010 Dec 14;75(24):2204-11. doi: 10.1212/WNL.0b013e318202038c.

3.

Asymmetry and heterogeneity of Alzheimer's and frontotemporal pathology in primary progressive aphasia.

Mesulam MM, Weintraub S, Rogalski EJ, Wieneke C, Geula C, Bigio EH.

Brain. 2014 Apr;137(Pt 4):1176-92. doi: 10.1093/brain/awu024. Epub 2014 Feb 25.

4.

Prediction of pathology in primary progressive language and speech disorders.

Deramecourt V, Lebert F, Debachy B, Mackowiak-Cordoliani MA, Bombois S, Kerdraon O, Buée L, Maurage CA, Pasquier F.

Neurology. 2010 Jan 5;74(1):42-9. doi: 10.1212/WNL.0b013e3181c7198e. Epub 2009 Nov 25.

PMID:
19940270
5.

Progressive nonfluent aphasia: a rare clinical subtype of FTLD-TDP in Japan.

Aoki N, Tsuchiya K, Kobayashi Z, Arai T, Togo T, Miyazaki H, Kondo H, Ishizu H, Uchikado H, Katsuse O, Hirayasu Y, Akiyama H.

Neuropathology. 2012 Jun;32(3):272-9. doi: 10.1111/j.1440-1789.2011.01253.x. Epub 2011 Oct 6.

PMID:
21978320
6.

Disruption of large-scale neural networks in non-fluent/agrammatic variant primary progressive aphasia associated with frontotemporal degeneration pathology.

Grossman M, Powers J, Ash S, McMillan C, Burkholder L, Irwin D, Trojanowski JQ.

Brain Lang. 2013 Nov;127(2):106-20. doi: 10.1016/j.bandl.2012.10.005. Epub 2012 Dec 4.

7.

Frontotemporal lobar degeneration: a clinical approach.

Karageorgiou E, Miller BL.

Semin Neurol. 2014 Apr;34(2):189-201. doi: 10.1055/s-0034-1381735. Epub 2014 Jun 25. Review.

PMID:
24963678
8.

Clinical and MRI correlates of disease progression in a case of nonfluent/agrammatic variant of primary progressive aphasia due to progranulin (GRN) Cys157LysfsX97 mutation.

Caso F, Agosta F, Magnani G, Galantucci S, Spinelli EG, Galimberti D, Falini A, Comi G, Filippi M.

J Neurol Sci. 2014 Jul 15;342(1-2):167-72. doi: 10.1016/j.jns.2014.03.058. Epub 2014 Apr 12.

PMID:
24814951
9.

White matter imaging helps dissociate tau from TDP-43 in frontotemporal lobar degeneration.

McMillan CT, Irwin DJ, Avants BB, Powers J, Cook PA, Toledo JB, McCarty Wood E, Van Deerlin VM, Lee VM, Trojanowski JQ, Grossman M.

J Neurol Neurosurg Psychiatry. 2013 Sep;84(9):949-55. doi: 10.1136/jnnp-2012-304418. Epub 2013 Mar 9.

10.
11.

Progressive nonfluent aphasia and its characteristic motor speech deficits.

Ogar JM, Dronkers NF, Brambati SM, Miller BL, Gorno-Tempini ML.

Alzheimer Dis Assoc Disord. 2007 Oct-Dec;21(4):S23-30. Review.

PMID:
18090419
12.

Frontal white matter tracts sustaining speech production in primary progressive aphasia.

Mandelli ML, Caverzasi E, Binney RJ, Henry ML, Lobach I, Block N, Amirbekian B, Dronkers N, Miller BL, Henry RG, Gorno-Tempini ML.

J Neurosci. 2014 Jul 16;34(29):9754-67. doi: 10.1523/JNEUROSCI.3464-13.2014.

13.

[Progressive nonfluent aphasia].

Murayama S, Saito Y.

Brain Nerve. 2011 Oct;63(10):1037-46. Review. Japanese.

PMID:
21987561
14.

Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?

Whitwell JL, Jack CR Jr, Parisi JE, Senjem ML, Knopman DS, Boeve BF, Rademakers R, Baker M, Petersen RC, Dickson DW, Josephs KA.

Neurology. 2010 Dec 14;75(24):2212-20. doi: 10.1212/WNL.0b013e31820203c2.

15.

Nonfluent/agrammatic PPA with in-vivo cortical amyloidosis and Pick's disease pathology.

Caso F, Gesierich B, Henry M, Sidhu M, LaMarre A, Babiak M, Miller BL, Rabinovici GD, Huang EJ, Magnani G, Filippi M, Comi G, Seeley WW, Gorno-Tempini ML.

Behav Neurol. 2013;26(1-2):95-106. doi: 10.3233/BEN-2012-120255.

16.

Caudate atrophy on MRI is a characteristic feature of FTLD-FUS.

Josephs KA, Whitwell JL, Parisi JE, Petersen RC, Boeve BF, Jack CR Jr, Dickson DW.

Eur J Neurol. 2010 Jul;17(7):969-75. doi: 10.1111/j.1468-1331.2010.02975.x. Epub 2010 Mar 3.

17.

MRI signatures of the frontotemporal lobar degeneration continuum.

Agosta F, Galantucci S, Magnani G, Marcone A, Martinelli D, Antonietta Volontè M, Riva N, Iannaccone S, Ferraro PM, Caso F, Chiò A, Comi G, Falini A, Filippi M.

Hum Brain Mapp. 2015 Jul;36(7):2602-14. doi: 10.1002/hbm.22794. Epub 2015 Mar 28.

PMID:
25821176
18.

MRI signatures of brain macrostructural atrophy and microstructural degradation in frontotemporal lobar degeneration subtypes.

Zhang Y, Tartaglia MC, Schuff N, Chiang GC, Ching C, Rosen HJ, Gorno-Tempini ML, Miller BL, Weiner MW.

J Alzheimers Dis. 2013;33(2):431-44. doi: 10.3233/JAD-2012-121156.

19.

Gray and white matter water diffusion in the syndromic variants of frontotemporal dementia.

Whitwell JL, Avula R, Senjem ML, Kantarci K, Weigand SD, Samikoglu A, Edmonson HA, Vemuri P, Knopman DS, Boeve BF, Petersen RC, Josephs KA, Jack CR Jr.

Neurology. 2010 Apr 20;74(16):1279-87. doi: 10.1212/WNL.0b013e3181d9edde.

20.

Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management.

Rabinovici GD, Miller BL.

CNS Drugs. 2010 May;24(5):375-98. doi: 10.2165/11533100-000000000-00000. Review.

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