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Neurodegenerative disease phenotypes in carriers of MAPT p.A152T, a risk factor for frontotemporal dementia spectrum disorders and Alzheimer disease.
Lee SE, Tartaglia MC, Yener G, Genç S, Seeley WW, Sanchez-Juan P, Moreno F, Mendez MF, Klein E, Rademakers R, López de Munain A, Combarros O, Kramer JH, Kenet RO, Boxer AL, Geschwind MD, Gorno-Tempini ML, Karydas AM, Rabinovici GD, Coppola G, Geschwind DH, Miller BL. Lee SE, et al. Among authors: geschwind dh, geschwind md. Alzheimer Dis Assoc Disord. 2013 Oct-Dec;27(4):302-9. doi: 10.1097/WAD.0b013e31828cc357. Alzheimer Dis Assoc Disord. 2013. PMID: 23518664 Free PMC article.
Commentary.
Wilhelmsen KC, Miller B, Geschwind D. Wilhelmsen KC, et al. Neurobiol Aging. 2001 Jan-Feb;22(1):119-21. doi: 10.1016/s0197-4580(00)00198-6. Neurobiol Aging. 2001. PMID: 11164284 No abstract available.
Association of GSK3B with Alzheimer disease and frontotemporal dementia.
Schaffer BA, Bertram L, Miller BL, Mullin K, Weintraub S, Johnson N, Bigio EH, Mesulam M, Wiedau-Pazos M, Jackson GR, Cummings JL, Cantor RM, Levey AI, Tanzi RE, Geschwind DH. Schaffer BA, et al. Among authors: geschwind dh. Arch Neurol. 2008 Oct;65(10):1368-74. doi: 10.1001/archneur.65.10.1368. Arch Neurol. 2008. PMID: 18852354 Free PMC article.
Functional genomic analysis of frataxin deficiency reveals tissue-specific alterations and identifies the PPARgamma pathway as a therapeutic target in Friedreich's ataxia.
Coppola G, Marmolino D, Lu D, Wang Q, Cnop M, Rai M, Acquaviva F, Cocozza S, Pandolfo M, Geschwind DH. Coppola G, et al. Among authors: geschwind dh. Hum Mol Genet. 2009 Jul 1;18(13):2452-61. doi: 10.1093/hmg/ddp183. Epub 2009 Apr 17. Hum Mol Genet. 2009. PMID: 19376812 Free PMC article.
579 results