Professor Stuart Pickering-Brown PhD

2011

• Baborie, A., Griffiths, T., Jaros, E., McKeith, I., Burn, D., Richardson, A., Ferrari, R., Moreno, J., Momeni, P., Duplessis, D., Pal, P., Rollinson, S., Pickering-Brown, S., Thompson, J., Neary, D., Snowden, J., Perry, R. & Mann, D (2011). Pathological correlates of frontotemporal lobar degeneration in the elderly. Acta Neuropathol, 121(3), 365-71. eScholarID:124724 | PMID:20978901 | DOI:10.1007/s00401-010-0765-z
• Chen-Plotkin, et al (2011). Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration. Arch Neurol, 68(4), 488-97. eScholarID:124729 | PMID:21482928 | DOI:10.1001/archneurol.2011.53
• Davidson, Y., Raby, S., Foulds, P., Robinson, A., Thompson, J., Sikkink, S., Yusuf, I., Amin, H., Duplessis, D., Troakes, C., Al-Sarraj, S., Sloan, C., Esiri, M., Prasher, V., Allsop, D., Neary, D., Pickering-Brown, S., Snowden, J. & Mann, D (2011). TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's Syndrome: association with age, hippocampal sclerosis and clinical phenotype. Acta Neuropathol, eScholarID:136593 | PMID:21968532 | DOI:10.1007/s00401-011-0879-y
• Höglinger, et al (2011). Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Nat Genet, eScholarID:124728 | PMID:21685912 | DOI:10.1038/ng.859
• Mok, K., Traynor, B., Schymick, J., Tienari, P., Laaksovirta, H., Peuralinna, T., Myllykangas, L., Chiò, A., Shatunov, A., Boeve, B., Boxer, A., Dejesus-Hernandez, M., Mackenzie, I., Waite, A., Williams, N., Morris, H., Simón-Sánchez, J., van Swieten, J., Heutink, P., Restagno, G., Mora, G., Morrison, K., Shaw, P., Rollinson, P., Al-Chalabi, A., Rademakers, R., Pickering-Brown, S., Orrell, R., Nalls, M. & Hardy, J (2011). The chromosome 9 ALS and FTD locus is probably derived from a single founder. Neurobiol Aging, eScholarID:136608 | PMID:21925771 | DOI:10.1016/j.neurobiolaging.2011.08.005
• Renton et al. (2011). A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron, 72(2), 257-268. eScholarID:149689 | DOI:10.1016/j.neuron.2011.09.010
• Renton, et al (2011). A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD. Neuron, 72(2), 257-68. eScholarID:136598 | PMID:21944779 | DOI:10.1016/j.neuron.2011.09.010
• Rollinson, S., Mead, S., Snowden, J., Richardson, A., Rohrer, J., Halliwell, N., Usher, S., Neary, D., Mann, D., Hardy, J. & Pickering-Brown, S (2011). Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis. Neurobiol Aging, eScholarID:118427 | PMID:21257233 | DOI:10.1016/j.neurobiolaging.2010.12.005
• Rollinson, S., Rohrer, J., van der Zee, J., Sleegers, K., Mead, S., Engelborghs, S., Collinge, J., De Deyn, P., Mann, D., Van Broeckhoven, C. & Pickering-Brown, S (2011). No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration. Neurobiol Aging, 32(4), 754-5. eScholarID:124725 | PMID:19446372 | DOI:10.1016/j.neurobiolaging.2009.04.009
• Snowden, J., Hu, Q., Rollinson, S., Halliwell, N., Robinson, A., Davidson, Y., Momeni, P., Baborie, A., Griffiths, T., Jaros, E., Perry, R., Richardson, A., Pickering-Brown, S., Neary, D. & Mann, D (2011). The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene. Acta Neuropathol, eScholarID:124727 | PMID:21424531 | DOI:10.1007/s00401-011-0816-0
• Stefani F, Zhang L, Taylor S, Donovan J, Rollinson S, Doyotte A, Brownhill K, Bennion J, Pickering-Brown S, Woodman P. (2011). UBAP1 Is a Component of an Endosome-Specific ESCRT-I Complex that Is Essential for MVB Sorting. Current Biology, eScholarID:127454 | DOI:10.1016/j.cub.2011.06.028

2010

• Baborie A, Griffiths TD, Jaros E, McKeith IG, Burn DJ, Richardson A, Ferrari R, Moreno J, Momeni P, Duplessis D, Pal P, Rollinson S, Pickering-Brown S, Thompson JC, Neary D, Snowden JS, Perry R, Mann DM. (2010). Pathological correlates of frontotemporal lobar degeneration in the elderly. Acta Neuropathol, eScholarID:96001
• Pickering-Brown, S (2010). Review: Recent progress in frontotemporal lobar degeneration. Neuropathol Appl Neurobiol, 36(1), 4-16. eScholarID:80517 | PMID:19821908 | DOI:10.1111/j.1365-2990.2009.01045.x
• Rollinson S, Bennion J, Toulson G, Halliwell N, Usher S, Snowden J, Richardson A, Neary D, Mann D, Pickering-Brown SM. (2010). Analysis of optineurin in frontotemporal lobar degeneration. Neurobiol Aging, eScholarID:105650
• Rollinson S, Bennion J, Toulson G, Halliwell N, Usher S, Snowden J, Richardson A, Neary D, Mann D, Pickering-Brown SM. (2010). Analysis of optineurin in frontotemporal lobar degeneration. Neurobiol Aging, eScholarID:96000
• Sara Rollinson, Simon Mead, Julie Snowden , Anna Richardson , Jonathan Rohrer, Nicola Halliwell, Suzanne Usher, David Neary, David Mann, John Hardy , Stuart Pickering-Brown. (2010). FTLD GWAS Replication confirms a risk locus shared with ALS. Neurobiol Aging, eScholarID:105653
• Urwin et al. (2010). FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration. Acta Neuropathol, 120(1), 33-41. eScholarID:96004 | DOI:10.1007/s00401-010-0698-6
• Van et al (2010). Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat Genet, 42(3), 234-9. eScholarID:80516 | PMID:20154673 | DOI:10.1038/ng.536
• Yokota O, Davidson Y, Arai T, Hasegawa M, Akiyama H, Ishizu H, Terada S, Sikkink S, Pickering-Brown S, Mann DM. (2010). Effect of topographical distribution of alpha-synuclein pathology on TDP-43 accumulation in Lewy body disease. Acta Neuropathol, eScholarID:96002
• Yokota O, Davidson Y, Bigio EH, Ishizu H, Terada S, Arai T, Hasegawa M, Akiyama H, Sikkink S, Pickering-Brown S, Mann DM. (2010). Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy. Acta Neuropathol, 120(1), 55-66. eScholarID:96003 | DOI:10.1007/s00401-010-0702-1

2009

• Colombo R, Tavian D, Baker MC, Richardson A, Snowden JS, Neary D, Mann DMA, Pickering-Brown S. (2009). Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration. Neurogenetics, eScholarID:1d19398 | DOI:10.1007/s10048-009-0189-x
• Davidson, YS, Amin, H, Kelley, T, Shi, J, Tian, J, Kumaran, R, Lashley, T, Lees, A, Duplessis, D, Neary, D, Snowden, JS, Akiyama, H, Arai, T, Hasegawa, M, Bandopadhyay, R, Sikkink, SSK, Pickering-Brown, S, Mann, DMA. (2009). TDP-43 in ubiquitinated inclusions in the inferior olives in frontotemporal lobar degeneration and in other neurodegenerative diseases: a degenerative process distinct from normal ageing. Acta Neuropathol, eScholarID:1d18909 | DOI:10.1007/s00401-009-0526-z
• Kelley, B, Haidar, W, Boeve, B, Baker, M, Graff-Radford, N, Krefft, T, Frank, A, Jack, C, Shiung, M, Knopman, D, Josephs, K, Parashos, S, Rademakers, R, Hutton, M, Pickering-Brown, S, Adamson, J, Kuntz, K, Dickson, D, Parisi, J, Smith, G, Ivnik, R, Petersen, R. (2009). Prominent phenotypic variability associated with mutations in Progranulin. Neurobiol Aging, 30( 5), eScholarID:1d19527 | DOI:10.1016/j.neurobiolaging.2007.08.022
• Rollinson, SJ, Rizzu, P, Sikkink, SSK, Baker, M, Halliwell, N, Snowden, JS, Traynor, B, Ruano, D, Cairns, N, Rohrer, J, Mead, S, Collinge, J, Rossor, M, Akay, E, Guerreiro, R, Rademakers, R, Morrison, K, Pastor, P, Alonso, E, Martinez-Lage, P, Graff-Radford, N, Neary, D, Heutink, P, Mann, DMA, Van Swieten, J, Pickering-Brown, S. (2009). Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration. Neurobiol Aging, eScholarID:1d18719 | DOI:10.1016/j.neurobiolaging.2009.01.009
• Rollinson, SJ, Rohrer, J, van der Zee, J, Sleegers, K, Mead, S, Engelborghs, S, Collinge, J, De Deyn, P, Mann, DMA, Van Broeckhoven, C, Pickering-Brown, S. (2009). No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration. Neurobiol Aging, eScholarID:1d19397 | DOI:10.1016/j.neurobiolaging.2009.04.009

2008

• Foulds P, McAuley E, Gibbons LC, Davidson YS, Pickering-Brown S, Neary D, Snowden JS, Allsop D, Mann DMA. (2008). TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer's disease and frontotemporal lobar degeneration. Acta Neuropathol, 116, 141-6. eScholarID:1d17331 | DOI:10.1007/s00401-008-0389-8
• Pickering-Brown S, Hutton M. (2008). The genetics of frontotemporal dementia. Handb Clin Neurol, 89, eScholarID:1d19524 | DOI:10.1016/S0072-9752(07)01236-5
• Pickering-Brown S, Rollinson S, Du Plessis DG, Morrison KE, Varma AR, Richardson A, Neary D, Snowden JS, Mann DMA. (2008). Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations. Brain, 131, eScholarID:1d16858 | DOI:10.1093/brain/awm331
• Rohrer, J, Warren, J, Omar, R, Mead, S, Beck, J, Revesz, T, Holton, J, Stevens, J, Al-Sarraj, S, Pickering-Brown, S, Hardy, J, Fox, N, Collinge, J, Warrington, E, Rossor, M. (2008). Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene. Arch Neurol, 65( 4), eScholarID:1d19525 | DOI:10.1001/archneur.65.4.506
• Snowden JS, Pickering-Brown S, Du Plessis DG, I R Mackenzie, Varma AR, Mann DMA, Neary D. (2008). Progressive Anomia revisited: focal degeneration associated with progranulin gene mutation. Neurocase, 13, 366-377. eScholarID:1d16866 | DOI:10.1080/13554790701851510

2007

• Davidson YS, Kelley T, McKenzie IRA, Pickering-Brown S, Du Plessis DG, Neary D, Snowden JS, Mann DMA. (2007). Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43. Acta Neuropathologica, 113, 521-533. eScholarID:1d15490 | DOI:10.1007/s00401-006-0189-y
• Davidson, Y, Gibbons, L, Pritchard, A, Hardicre, J, Wren, J, Stopford, C, Julien, C, Thompson, J, Payton, A, Pickering-Brown, S, Pendleton, N, Horan, M A, Burns, AS, Purandare, N, Lendon, C, Neary, D, Snowden, JS, Mann, D. (2007). Apolipoprotein E epsilon4 allele frequency and age at onset of Alzheimer's disease. Dement Geriatr Cogn Disord, 23( 1), eScholarID:1d16917
• Doran M, Du Plessis DG, Ghadiali E, Mann DMA, Pickering-Brown S, Larner A. (2007). Familial early-onset dementia with tau intron 10 + 16 mutation with clinical features similar to those of Alzheimer disease. Arch Neurol, 64( 10), 1535-1539. eScholarID:1d16830
• Pickering-Brown S. (2007). Progranulin and frontotemporal lobar degeneration. Acta Neuropathol, 114( 1), eScholarID:1d19533 | DOI:10.1007/s00401-007-0241-6
• Pickering-Brown S. (2007). The complex aetiology of frontotemporal lobar degeneration. Exp Neurol, 206( 1), eScholarID:1d19534 | DOI:10.1016/j.expneurol.2007.03.017
• Rademakers, et al. (2007). Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. Lancet Neurol, 6( 10), 857-68. eScholarID:1d16863
• Rollinson S, Snowden JS, Neary D, Morrison K E, Mann DMA, Pickering-Brown S. (2007). TDP-43 gene analysis in frontotemporal lobar degeneration. Neurosci Lett, 419, eScholarID:1d33280
• Sikkink SSK, Rollinson SJ, Pickering-Brown S. (2007). The genetics of frontotemporal lobar degeneration. Curr Opin Neurol, 20( 6), eScholarID:1d19526 | DOI:10.1097/WCO.0b013e3282f1c961
• Zhang Y, Xu Y, Dickey C, Buratti E, Baralle F, Bailey R, Pickering-Brown S, Dickson D, Petrucelli L. (2007). Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43. J Neurosci, 27( 39), eScholarID:1d19532 | DOI:10.1523/JNEUROSCI.3421-07.2007

2006

• Baker, M, Mackenzie, I, Pickering-Brown, S, Gass, J, Rademakers, R, Lindholm, C, Snowden, JS, Adamson, J, Sadovnick, A, Rollinson, S, Cannon, A, Dwosh, E, Neary, D, Melquist, S, Richardson, A, Dickson, D, Berger, Z, Eriksen, J, Robinson, T, Zehr, C, Dickey, C, Crook, R, McGowan, E, Mann, DMA, Boeve, B, Feldman, H, Hutton, M. (2006). Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature, 442( 7105), eScholarID:1d13701 | DOI:10.1038/nature05016
• Cannon A, Baker M, Boeve B, Josephs K, Knopman D, Peterson R, Dickson D, Adamson J, Snowden, JS, Neary, D, Mann, DMA, Hutton M, Pickering-Brown, S. (2006). CHMP2B mutations are not a common cause of Fontotemporal Lobar Degeneration. Neurosci Lett, 398, eScholarID:1d32811
• Cannon, A, Baker, M, Boeve, B, Josephs, K, Knopman, D, Petersen, R, Parisi, J, Dickison, D, Adamson, J, Snowden, J, Snowden, JS, Neary, D, Mann, D, Hutton, M, Pickering-Brown, S. (2006). CHMP2B mutations are not a common cause of frontotemporal lobar degeneration. Neurosci Lett, eScholarID:1d30049
• Davidson, YS, Gibbons, LC, Pritchard A H, Hardicre, J, Wren, J, Tian, J, Shi, J, Stopford, C, Julien, C, Thompson, J, Payton, A, Thaker, U, Hayes, A, Iwatsubo, T, Pickering-Brown, S, Pendleton, N, Horan, M A, Burns, AS, Purandare, N, Lendon, C, Neary, D, Snowden, JS, Mann, DMA. (2006). Genetic associations between cathepsin D exon 2 C->T polymorphism and Alzheimer's disease, and pathological correlations with genotype. J Neurol Neurosurg Psychiatry, 77( 4), eScholarID:1d12924
• de Silva, R, Lashley, T, Strand, C, Shiarli, A, Shi, J, Tian, J, Bailey, K, Davies, P, Bigio, E, Arima, K, Iseki, E, Murayama, S, Kretzschmar, H, Neumann, M, Lippa, C, Halliday, G, Mackenzie, J, Ravid, R, Dickson, D, Wszolek, Z, Iwatsubo, T, Pickering-Brown, S, Holton, J, Lees, A, Revesz, T, Mann, D. (2006). An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies. Acta Neuropathol (Berl), eScholarID:1d29952
• Mackenzie I R A, Baborie A, Pickering-Brown S, Du Plessis DG, Jaros E, Perry R H, Neary D, Snowden JS, Mann DMA. (2006). Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype. Acta Neuropathol, 112, 539-549. eScholarID:1d13607 | DOI:10.1007/s00401-006-0138-9
• Mackenzie, I, Baker, M, West, G, Woulfe, J, Qadi, N, Gass, J, Cannon, A, Adamson, J, Feldman, H, Lindholm, C, Melquist, S, Pettman, R, Sadovnick, A, Dwosh, E, Whiteheart, S, Hutton, M, Pickering-Brown, S. (2006). A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17. Brain, 129( Pt 4), eScholarID:1d12928 | DOI:10.1093/brain/awh724
• Momeni P, Bell J, Duckworth J, Hutton M, Mann DMA, Pickering-Brown S, Hardy J. (2006). Sequence analysis of all identified open reading frames on the frontal temporal dementia haplotype on chromosome 3 fails to identify unique coding variants except in CHMP2B. Neurosci Lett, 410, eScholarID:1d32964
• Pickering-Brown, S, Baker M, Gass J, Boeve BF, Loy CT, Brooks WS, Mackenzie IR, Martins RN, Kwok JB, Halliday GM, Kril JJ, Shofield PR, Mann, DMA, Hutton M. (2006). Mutations in progranulin explain atypical phenotypes with variants in MAPT. Brain, 129, eScholarID:1d14099 | DOI:10.1093/brain/awl289
• Shiarli A M, Jennings R, Shi J, Bailey K, Davidson, YS, Tian J, Bigio E, Ghetti B, Arima K, Iseki E, Murayama S, Kretzchmar H, Lippa C, Halliday G, MacKenzie J, Khan N, Ravid R, Dickson D, Wszolek Z, Iwatsubo T, Pickering-Brown, S, Mann, DMA. (2006). Comparative tau pathology in Frontotemporal Lobar Degeneration and Alzheimer's disease. Neuropathology and Applied Neurobiology, 32, 374-387. eScholarID:1d13584 | DOI:10.1111/j.1365-2990.2006.00736.x
• Shiarli, A, Jennings, R, Shi, J, Bailey, K, Davidson, Y, Tian, J, Bigio, E, Ghetti, B, Murrell, J, Delisle, M, Mirra, S, Crain, B, Zolo, P, Arima, K, Iseki, E, Murayama, S, Kretzschmar, H, Neumann, M, Lippa, C, Halliday, G, Mackenzie, J, Khan, N, Ravid, R, Dickson, D, Wszolek, Z, Iwatsubo, T, Pickering-Brown, S, Mann, D. (2006). Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease. Neuropathol Appl Neurobiol, 32( 4), 374-87. eScholarID:1d29990
• Snowden JS, Pickering-Brown S, Mackenzie I R, Richardson A M T, Varma A, Neary D, Mann DMA. (2006). Progranulin gene mutations associated with frontotemporal dementia and progressive aphasia. Brain, 129, 3091-3102. eScholarID:1d13609 | DOI:10.1093/brain/awl267
• Srinivasan, R, Davidson, Y, Gibbons, L, Payton, A, Richardson, A, Varma, A, Julien, C, Stopford, C, Thompson, J, Horan, M, Pendleton, N, Pickering-Brown, S, Neary, D, Snowden, JS, Mann, D. (2006). The apolipoprotein E epsilon4 allele selectively increases the risk of frontotemporal lobar degeneration in males. J Neurol Neurosurg Psychiatry, 77( 2), 154-8. eScholarID:1d12927
• Wszolek Z, Tsuboi Y, Ghetti B, Pickering-Brown S, Baba Y, Cheshire W. (2006). Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Orphanet J Rare Dis, 1, eScholarID:1d30158

2005

• Baba, Y, Tsuboi, Y, Baker, M, Uitti, R, Hutton, M, Dickson, D, Farrer, M, Putzke, J, Woodruff, B, Ghetti, B, Murrell, J, Boeve, B, Petersen, R, Verpillat, P, Brice, A, Delisle, M, Rascol, O, Arima, K, Dysken, M, Yasuda, M, Kobayashi, T, Sunohara, N, Komure, O, Kuno, S, Sperfeld, A, Stoppe, G, Kohlhase, J, Pickering-Brown, S, Neary, D, Bugiani, O, Wszolek, Z. (2005). The effect of tau genotype on clinical features in FTDP-17. Parkinsonism Relat Disord, 11( 4), eScholarID:1d30310
• Shi, J, Shaw, C, Du Plessis, DG, Richardson, A, Bailey, K, Julien, C, Stopford, C, Thompson, J, Varma, A, Craufurd, D, Tian, J, Pickering-Brown, S, Neary, D, Snowden, JS, Mann, DMA. (2005). Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation. Acta Neuropathol (Berl), 110( 5), 501-12. eScholarID:1d12930

2004

• Pickering-Brown, S, Baker, M, Nonaka, T, Ikeda, K, Sharma, S, Mackenzie, J, Simpson, S, Moore, J, Snowden, JS, de Silva, R, Revesz, T, Hasegawa, M, Hutton, M, Mann, D. (2004). Frontotemporal dementia with Pick-type histology associated with Q336R mutation in the tau gene. Brain, 127( Pt 6), 1415-26. eScholarID:1d12130 | DOI:10.1093/brain/awh147
• Taniguchi S, McDonagh A, Pickering-Brown S, Umeda Y, Iwatsubo T, Hasegawa M, Mann D. (2004). The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein. Neuropathol Appl Neurobiol, 30( 1), 1-18. eScholarID:1d30773

2002

• Pickering-Brown, S, Richardson, A, Snowden, JS, McDonagh, A, Burns, A, Braude, W, Baker, M, Liu, W, Yen, S, Hardy, J, Hutton, M, Davies, Y, Allsop, D, Craufurd, D, Neary, D, Mann, D. (2002). Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene. Brain, 125( Pt 4), 732-51. eScholarID:1d31121
• Pickering-Brown, S, Richardson, AM, Snowden, JS, McDonagh, AM, Burns, AS, Braude, W, Baker, M, Liu, WK, Yen, SH, Hardy, J, Hutton, M, Davies,Y, Allop, D, Craufurd, D, Neary, D, Mann, DMA. (2002). Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene. Brain, 125 (4), eScholarID:1d3989
• Zhukareva, V, Mann, DMA, Pickering-Brown, S, Uryu, K, Shuck, T, Shah, K, Grossman, M, Miller, B, Hulette, C, Feinstein, S, Trojanowski, J, Lee, V. (2002). Sporadic Pick's disease: a tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matter. Ann Neurol, 51( 6), 730-9. eScholarID:1d30225

2001

• Mann D, Pickering-Brown S, Takeuchi A, Iwatsubo T. (2001). Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease. Am J Pathol, 158( 6), eScholarID:1d30029