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Page 1
Cortical and subcortical pathological burden and neuronal loss in an autopsy series of FTLD-TDP-type C.
Kawles A, Nishihira Y, Feldman A, Gill N, Minogue G, Keszycki R, Coventry C, Spencer C, Lilek J, Ajroud K, Coppola G, Rademakers R, Rogalski E, Weintraub S, Zhang H, Flanagan ME, Bigio EH, Mesulam MM, Geula C, Mao Q, Gefen T. Kawles A, et al. Among authors: ajroud k. Brain. 2022 Apr 29;145(3):1069-1078. doi: 10.1093/brain/awab368. Brain. 2022. PMID: 34919645 Free PMC article.
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Deng HX, Chen W, Hong ST, Boycott KM, Gorrie GH, Siddique N, Yang Y, Fecto F, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen GH, Donkervoort S, Bigio EH, Brooks BR, Ajroud K, Sufit RL, Haines JL, Mugnaini E, Pericak-Vance MA, Siddique T. Deng HX, et al. Among authors: ajroud k. Nature. 2011 Aug 21;477(7363):211-5. doi: 10.1038/nature10353. Nature. 2011. PMID: 21857683 Free PMC article.
Primary Progressive Aphasia has a Unique Signature Distinct from Dementia of the Alzheimer's Type and Behavioral Variant Frontotemporal Dementia Regardless of Pathology.
Gefen T, Mao Q, Kohler M, Moeller S, Kawles A, Coventry C, Spencer C, Lilek J, Ajroud K, Feldman A, Flanagan M, Rogalski E, Weintraub S, Rademaker A, Geula C, Mesulam MM, Bigio E. Gefen T, et al. Among authors: ajroud k. J Neuropathol Exp Neurol. 2020 Dec 4;79(12):1379-1381. doi: 10.1093/jnen/nlaa080. J Neuropathol Exp Neurol. 2020. PMID: 33068393 Free PMC article. No abstract available.
Accumulation of pTau231 at the Postsynaptic Density in Early Alzheimer's Disease.
Lilek J, Ajroud K, Feldman AZ, Krishnamachari S, Ghourchian S, Gefen T, Spencer CL, Kawles A, Mao Q, Tranovich JF, Jack CR, Mesulam MM, Reichard RR, Zhang H, Murray ME, Knopman D, Dickson DW, Petersen RC, Smith B, Ashe KH, Mielke MM, Nelson KM, Flanagan ME. Lilek J, et al. Among authors: ajroud k. J Alzheimers Dis. 2023;92(1):241-260. doi: 10.3233/JAD-220848. J Alzheimers Dis. 2023. PMID: 36744338 Free PMC article.
A novel de novo MFN2 mutation causing CMT2A with upper motor neuron signs.
Ajroud-Driss S, Fecto F, Ajroud K, Yang Y, Donkervoort S, Siddique N, Siddique T. Ajroud-Driss S, et al. Among authors: ajroud k. Neurogenetics. 2009 Oct;10(4):359-61. doi: 10.1007/s10048-009-0188-y. Epub 2009 Apr 7. Neurogenetics. 2009. PMID: 19350291 No abstract available.
12 results