Review: Clinical, neuropathological and genetic features of Lewy body dementias von Hansen, D., Ling, H., Lashley, T., Holton, J. L., Warner, T. T.

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Lewy- and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important? von COMPTA, Yaroslau, PARKKINEN, Laura, LEERS, Andrew J, REVESZ, Tamas, O'SULLIVAN, Sean S, VANDROVCOVA, Jana, HOLTON, Janice L, COLLINS, Catherine, LASHLEY, Tammaryn, KALLIS, Constantinos, WILLIAMS, David R, DE SILVA, Rohan

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Novel clinicopathological characteristics differentiate dementia with Lewy bodies from Parkinson’s disease dementia von Hansen, D., Ling, H., Lashley, T., Foley, J. A., Strand, C., Eid, T. M., Holton, J. L., Warner, T. T.

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Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration von Rohrer, Jonathan D., Lashley, Tammaryn, Schott, Jonathan M., Warren, Jane E., Mead, Simon, Isaacs, Adrian M., Beck, Jonathan, Hardy, John, de Silva, Rohan, Warrington, Elizabeth, Troakes, Claire, Al-Sarraj, Safa, King, Andrew, Borroni, Barbara, Clarkson, Matthew J., Ourselin, Sebastien, Holton, Janice L., Fox, Nick C., Revesz, Tamas, Rossor, Martin N., Warren, Jason D.

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Frontotemporal lobar degenerations: from basic science to clinical manifestations von Revesz, T., Mann, D. M., Lashley, T.

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APOE ε4 is also required in TREM2 R47H variant carriers for Alzheimer's disease to develop von Murray, C. E., King, A., Troakes, C., Hodges, A., Lashley, T.

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Corticospinal tract degeneration and temporal lobe atrophy in frontotemporal lobar degeneration TDP‐43 type C pathology von Miki, Y., Ling, H., Crampsie, S., Mummery, C. J., Rohrer, J. D., Jaunmuktane, Z., Lashley, T., Holton, J. L.

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Cerebral amyloidosis: amyloid subunits, mutants and phenotypes von Rostagno, A., Holton, J. L., Lashley, T., Revesz, T., Ghiso, Jorge

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A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies von Lashley, Tammaryn, Rohrer, Jonathan D., Bandopadhyay, Rina, Fry, Charles, Ahmed, Zeshan, Isaacs, Adrian M., Brelstaff, Jack H., Borroni, Barbara, Warren, Jason D., Troakes, Claire, King, Andrew, Al-Saraj, Safa, Newcombe, Jia, Quinn, Niall, Ostergaard, Karen, Schrøder, Henrik Daa, Bojsen-Møller, Marie, Braendgaard, Hans, Fox, Nick C., Rossor, Martin N., Lees, Andrew J., Holton, Janice L., Revesz, Tamas

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LRRK2 expression in idiopathic and G2019S positive Parkinson's disease subjects: a morphological and quantitative study von Sharma, S., Bandopadhyay, R., Lashley, T., Renton, A. E. M., Kingsbury, A. E., Kumaran, R., Kallis, C., Vilariño-Güell, C., O'Sullivan, S. S., Lees, A. J., Revesz, T., Wood, N. W., Holton, J. L.

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The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degeneration von Rohrer, Jonathan D, Lashley, Tammaryn, Holton, Janice, Revesz, Tamas, Urwin, Hazel, Isaacs, Adrian M, Fox, Nick C, Rossor, Martin N, Warren, Jason

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Genetic Alterations of the BRI2 gene: Familial British and Danish Dementias von J, Ghiso, A, Rostagno, Y, Tomidokoro, T, Lashley, M, Bojsen-Møller, H, Braendgaard, G, Plant, J, Holton, R, Lal, T, Revesz, B, Frangione

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Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal an... von De Silva, R., Lashley, T., Gibb, G., Hanger, D., Hope, A., Reid, A., Bandopadhyay, R., Utton, M., Strand, C., Jowett, T., Khan, N., Anderton, B., Wood, N., Holton, J., Revesz, T., Lees, A.

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Chromosome 13 dementias von Rostagno, A, Tomidokoro, Y, Lashley, T, Ng, D, Plant, G, Holton, J, Frangione, B, Revesz, T, Ghiso, J

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Mass Spectrometric Analysis of Lewy Body-Enriched α‑Synuclein in Parkinson’s Disease von Bhattacharjee, Payel, Öhrfelt, Annika, Lashley, Tammaryn, Blennow, Kaj, Brinkmalm, Ann, Zetterberg, Henrik

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Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations von Lashley, Tammaryn, Rohrer, Jonathan D., Mead, Simon, Revesz, Tamas

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Familial Alzheimer’s disease patient-derived neurons reveal distinct mutation-specific effects on amyloid beta von Arber, Charles, Toombs, Jamie, Lovejoy, Christopher, Ryan, Natalie S., Paterson, Ross W., Willumsen, Nanet, Gkanatsiou, Eleni, Portelius, Erik, Blennow, Kaj, Heslegrave, Amanda, Schott, Jonathan M., Hardy, John, Lashley, Tammaryn, Fox, Nick C., Zetterberg, Henrik, Wray, Selina

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Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy von MORRIS, H. R, GIBB, G, REVESZ, T, KATZENSCHLAGER, R, WOOD, N. W, HANGER, D. P, STRAND, C, LASHLEY, T, DANIEL, S. E, LEES, A. J, ANDERTON, B. H

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Molecular biomarkers of Alzheimer's disease: progress and prospects von Lashley, Tammaryn, Schott, Jonathan M, Weston, Philip, Murray, Christina E, Wellington, Henny, Keshavan, Ashvini, Foti, Sandrine C, Foiani, Martha, Toombs, Jamie, Rohrer, Jonathan D, Heslegrave, Amanda, Zetterberg, Henrik

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Expression of BRI2 mRNA and protein in normal human brain and familial British dementia: its relevance to the pathogenesis of disease von Lashley, T., Revesz, T., Plant, G., Bandopadhyay, R., Lees, A. J., Frangione, B., Wood, N. W., De Silva, R., Ghiso, J., Rostagno, A., Holton, J. L.

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