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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2006 | 2 |
2008 | 1 |
2024 | 0 |
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Page 1
Analysis of UBQLN1 variants in a Polish Alzheimer's disease patient: control series.
Dement Geriatr Cogn Disord. 2008;25(4):366-71. doi: 10.1159/000121006. Epub 2008 Mar 14.
Dement Geriatr Cogn Disord. 2008.
PMID: 18340109
A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17.
Mackenzie IR, Baker M, West G, Woulfe J, Qadi N, Gass J, Cannon A, Adamson J, Feldman H, Lindholm C, Melquist S, Pettman R, Sadovnick AD, Dwosh E, Whiteheart SW, Hutton M, Pickering-Brown SM.
Mackenzie IR, et al.
Brain. 2006 Apr;129(Pt 4):853-67. doi: 10.1093/brain/awh724. Epub 2006 Jan 9.
Brain. 2006.
PMID: 16401619
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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
Gass J, Cannon A, Mackenzie IR, Boeve B, Baker M, Adamson J, Crook R, Melquist S, Kuntz K, Petersen R, Josephs K, Pickering-Brown SM, Graff-Radford N, Uitti R, Dickson D, Wszolek Z, Gonzalez J, Beach TG, Bigio E, Johnson N, Weintraub S, Mesulam M, White CL 3rd, Woodruff B, Caselli R, Hsiung GY, Feldman H, Knopman D, Hutton M, Rademakers R.
Gass J, et al.
Hum Mol Genet. 2006 Oct 15;15(20):2988-3001. doi: 10.1093/hmg/ddl241. Epub 2006 Sep 1.
Hum Mol Genet. 2006.
PMID: 16950801
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