Yuan W - Search Results

1

Amyotrophic lateral sclerosis-plus syndrome with TAR DNA-binding protein-43 pathology.

McCluskey LF, Elman LB, Martinez-Lage M, Van Deerlin V, Yuan W, Clay D, Siderowf A, Trojanowski JQ. McCluskey LF, et al. Among authors: yuan w. Arch Neurol. 2009 Jan;66(1):121-4. doi: 10.1001/archneur.66.1.121. Arch Neurol. 2009. PMID: 19139310 Free PMC article.

2

Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.

Chen-Plotkin AS, Yuan W, Anderson C, McCarty Wood E, Hurtig HI, Clark CM, Miller BL, Lee VM, Trojanowski JQ, Grossman M, Van Deerlin VM. Chen-Plotkin AS, et al. Among authors: yuan w. Neurology. 2008 Feb 12;70(7):521-7. doi: 10.1212/01.WNL.0000280574.17166.26. Epub 2007 Oct 3. Neurology. 2008. PMID: 17914064 Free PMC article.

3

Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations.

Van Deerlin VM, Wood EM, Moore P, Yuan W, Forman MS, Clark CM, Neumann M, Kwong LK, Trojanowski JQ, Lee VM, Grossman M. Van Deerlin VM, et al. Among authors: yuan w. Arch Neurol. 2007 Aug;64(8):1148-53. doi: 10.1001/archneur.64.8.1148. Arch Neurol. 2007. PMID: 17698705

4

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.

Van Deerlin VM, Leverenz JB, Bekris LM, Bird TD, Yuan W, Elman LB, Clay D, Wood EM, Chen-Plotkin AS, Martinez-Lage M, Steinbart E, McCluskey L, Grossman M, Neumann M, Wu IL, Yang WS, Kalb R, Galasko DR, Montine TJ, Trojanowski JQ, Lee VM, Schellenberg GD, Yu CE. Van Deerlin VM, et al. Among authors: yuan w. Lancet Neurol. 2008 May;7(5):409-16. doi: 10.1016/S1474-4422(08)70071-1. Epub 2008 Apr 7. Lancet Neurol. 2008. PMID: 18396105 Free PMC article.

5

Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration.

Chen-Plotkin AS, Geser F, Plotkin JB, Clark CM, Kwong LK, Yuan W, Grossman M, Van Deerlin VM, Trojanowski JQ, Lee VM. Chen-Plotkin AS, et al. Among authors: yuan w. Hum Mol Genet. 2008 May 15;17(10):1349-62. doi: 10.1093/hmg/ddn023. Epub 2008 Jan 25. Hum Mol Genet. 2008. PMID: 18223198 Free PMC article.

6

A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro.

Winton MJ, Van Deerlin VM, Kwong LK, Yuan W, Wood EM, Yu CE, Schellenberg GD, Rademakers R, Caselli R, Karydas A, Trojanowski JQ, Miller BL, Lee VM. Winton MJ, et al. Among authors: yuan w. FEBS Lett. 2008 Jun 25;582(15):2252-6. doi: 10.1016/j.febslet.2008.05.024. Epub 2008 May 27. FEBS Lett. 2008. PMID: 18505686 Free PMC article.

7

Clinical and pathological characteristics of patients with leucine-rich repeat kinase-2 mutations.

Covy JP, Yuan W, Waxman EA, Hurtig HI, Van Deerlin VM, Giasson BI. Covy JP, et al. Among authors: yuan w. Mov Disord. 2009 Jan 15;24(1):32-9. doi: 10.1002/mds.22096. Mov Disord. 2009. PMID: 19006185 Free PMC article.

8

Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer disease.

Brickell KL, Steinbart EJ, Rumbaugh M, Payami H, Schellenberg GD, Van Deerlin V, Yuan W, Bird TD. Brickell KL, et al. Among authors: yuan w. Arch Neurol. 2006 Sep;63(9):1307-11. doi: 10.1001/archneur.63.9.1307. Arch Neurol. 2006. PMID: 16966510

9

Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease.

Brickell KL, Leverenz JB, Steinbart EJ, Rumbaugh M, Schellenberg GD, Nochlin D, Lampe TH, Holm IE, Van Deerlin V, Yuan W, Bird TD. Brickell KL, et al. Among authors: yuan w. J Neurol Neurosurg Psychiatry. 2007 Oct;78(10):1050-5. doi: 10.1136/jnnp.2006.113803. Epub 2007 Jul 5. J Neurol Neurosurg Psychiatry. 2007. PMID: 17615170 Free PMC article.

10

Genetic variability in CHMP2B and frontotemporal dementia.

Momeni P, Rogaeva E, Van Deerlin V, Yuan W, Grafman J, Tierney M, Huey E, Bell J, Morris CM, Kalaria RN, van Rensburg SJ, Niehaus D, Potocnik F, Kawarai T, Salehi-Rad S, Sato C, St George-Hyslop P, Hardy J. Momeni P, et al. Among authors: yuan w. Neurodegener Dis. 2006;3(3):129-33. doi: 10.1159/000094771. Neurodegener Dis. 2006. PMID: 16954699

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