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Items: 1 to 20 of 99

1.

Atrophy and microglial distribution in primary progressive aphasia with transactive response DNA-binding protein-43 kDa.

Kim G, Bolbolan K, Gefen T, Weintraub S, Bigio EH, Rogalski E, Mesulam MM, Geula C.

Ann Neurol. 2018 Jun;83(6):1096-1104. doi: 10.1002/ana.25240. Epub 2018 May 24.

2.

Asymmetric TDP pathology in primary progressive aphasia with right hemisphere language dominance.

Kim G, Vahedi S, Gefen T, Weintraub S, Bigio EH, Mesulam MM, Geula C.

Neurology. 2018 Jan 30;90(5):e396-e403. doi: 10.1212/WNL.0000000000004891. Epub 2018 Jan 5.

3.

Asymmetric pathology in primary progressive aphasia with progranulin mutations and TDP inclusions.

Kim G, Ahmadian SS, Peterson M, Parton Z, Memon R, Weintraub S, Rademaker A, Bigio E, Mesulam MM, Geula C.

Neurology. 2016 Feb 16;86(7):627-36. doi: 10.1212/WNL.0000000000002375. Epub 2016 Jan 20.

4.

Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation.

Gliebus G, Bigio EH, Gasho K, Mishra M, Caplan D, Mesulam MM, Geula C.

Neurology. 2010 May 18;74(20):1607-10. doi: 10.1212/WNL.0b013e3181df0a1b.

5.

Prominent microglial activation in cortical white matter is selectively associated with cortical atrophy in primary progressive aphasia.

Ohm DT, Kim G, Gefen T, Rademaker A, Weintraub S, Bigio EH, Mesulam MM, Rogalski E, Geula C.

Neuropathol Appl Neurobiol. 2019 Apr;45(3):216-229. doi: 10.1111/nan.12494. Epub 2018 May 17.

PMID:
29679378
6.

Morphology and Distribution of TDP-43 Pre-inclusions in Primary Progressive Aphasia.

Kim G, Bolbolan K, Shahidehpour R, Jamshidi P, Gefen T, Ayala IA, Weintraub S, Bigio EH, Mesulam MM, Geula C.

J Neuropathol Exp Neurol. 2019 Mar 1;78(3):229-237. doi: 10.1093/jnen/nlz005.

PMID:
30753613
7.

Typical and atypical pathology in primary progressive aphasia variants.

Spinelli EG, Mandelli ML, Miller ZA, Santos-Santos MA, Wilson SM, Agosta F, Grinberg LT, Huang EJ, Trojanowski JQ, Meyer M, Henry ML, Comi G, Rabinovici G, Rosen HJ, Filippi M, Miller BL, Seeley WW, Gorno-Tempini ML.

Ann Neurol. 2017 Mar;81(3):430-443. doi: 10.1002/ana.24885. Epub 2017 Mar 20.

8.

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.

9.

Mixed tau and TDP-43 pathology in a patient with unclassifiable primary progressive aphasia.

Flanagan EP, Duffy JR, Whitwell JL, Vemuri P, Dickson DW, Josephs KA.

Neurocase. 2016;22(1):55-9. doi: 10.1080/13554794.2015.1041534. Epub 2015 May 1.

10.

TDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer disease.

Bigio EH, Mishra M, Hatanpaa KJ, White CL 3rd, Johnson N, Rademaker A, Weitner BB, Deng HX, Dubner SD, Weintraub S, Mesulam M.

Acta Neuropathol. 2010 Jul;120(1):43-54. doi: 10.1007/s00401-010-0681-2. Epub 2010 Apr 2.

11.
12.

Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia.

Mesulam M, Wicklund A, Johnson N, Rogalski E, Léger GC, Rademaker A, Weintraub S, Bigio EH.

Ann Neurol. 2008 Jun;63(6):709-19. doi: 10.1002/ana.21388.

13.

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
14.

Primary progressive aphasia and Alzheimer's disease: brief history, recent evidence.

Kirshner HS.

Curr Neurol Neurosci Rep. 2012 Dec;12(6):709-14. doi: 10.1007/s11910-012-0307-2. Review.

PMID:
22932755
15.

Patterns of Microglial Cell Activation in Alzheimer Disease and Frontotemporal Lobar Degeneration.

Taipa R, Brochado P, Robinson A, Reis I, Costa P, Mann DM, Melo Pires M, Sousa N.

Neurodegener Dis. 2017;17(4-5):145-154. doi: 10.1159/000457127. Epub 2017 Apr 27.

PMID:
28445885
16.

An autopsy case of frontotemporal lobar degeneration with the appearance of fused in sarcoma inclusions (basophilic inclusion body disease) clinically presenting corticobasal syndrome.

Matsumoto A, Suzuki H, Fukatsu R, Shimizu H, Suzuki Y, Hisanaga K.

Neuropathology. 2016 Feb;36(1):77-87. doi: 10.1111/neup.12232. Epub 2015 Jul 31.

PMID:
26227957
17.

Cortical degeneration in frontotemporal lobar degeneration with TDP-43 proteinopathy caused by progranulin gene mutation.

Armstrong RA.

Int J Neurosci. 2014 Dec;124(12):894-903. doi: 10.3109/00207454.2014.890620. Epub 2014 Mar 3.

PMID:
24494724
19.

Neuron loss and degeneration in the progression of TDP-43 in frontotemporal lobar degeneration.

Yousef A, Robinson JL, Irwin DJ, Byrne MD, Kwong LK, Lee EB, Xu Y, Xie SX, Rennert L, Suh E, Van Deerlin VM, Grossman M, Lee VM, Trojanowski JQ.

Acta Neuropathol Commun. 2017 Sep 6;5(1):68. doi: 10.1186/s40478-017-0471-3.

20.

Neurocognitive speed associates with frontotemporal lobar degeneration TDP-43 subtypes.

Dean PM, Smith GE, Parisi JE, Dickson DW, Petersen RC, Josephs KA.

J Clin Neurosci. 2013 Dec;20(12):1737-41. doi: 10.1016/j.jocn.2013.01.024. Epub 2013 Sep 4.

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