A clinico-pathological study of subtypes in Parkinson's disease von Selikhova, M., Williams, D. R., Kempster, P. A., Holton, J. L., Revesz, T., Lees, A. J.

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The neuropathology, pathophysiology and genetics of multiple system atrophy von Ahmed, Z., Asi, Y. T., Sailer, A., Lees, A. J., Houlden, H., Revesz, T., Holton, J. L.

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Proposed neuropathological criteria for the post mortem diagnosis of multiple system atrophy von Trojanowski, J. Q., Revesz, 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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Relationships between age and late progression of Parkinson’s disease: a clinico-pathological study von Kempster, Peter A., O’Sullivan, Sean S., Holton, Janice L., Revesz, Tamas, Lees, Andrew J.

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Clinical outcomes of progressive supranuclear palsy and multiple system atrophy von O'Sullivan, S. S., Massey, L. A., Williams, D. R., Silveira-Moriyama, L., Kempster, P. A., Holton, J. L., Revesz, T., Lees, A. J.

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Evolving concepts of chronic traumatic encephalopathy as a neuropathological entity von Ling, H., Neal, J. W., Revesz, T.

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Second consensus statement on the diagnosis of multiple system atrophy von GILMAN, S, WENNING, G. K, KAUFMANN, H, KLOCKGETHER, T, LEES, A, POEWE, W, QUINN, N, REVESZ, T, ROBERTSON, D, SANDRONI, P, SEPPI, K, VIDAILHET, M, LOW, P. A, BROOKS, D. J, MATHIAS, C. J, TROJANOWSKI, J. Q, WOOD, N. W, COLOSIMO, C, DÜRR, A, FOWLER, C. J

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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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The heritability and genetics of frontotemporal lobar degeneration von ROHRER, J. D, GUERREIRO, R, MACKENZIE, I. R. A, WARREN, J. D, DE SILVA, R, HOLTON, J, REVESZ, T, HARDY, J, MEAD, S, ROSSOR, M. N, VANDROVCOVA, J, UPHILL, J, REIMAN, D, BECK, J, ISAACS, A. M, AUTHIER, A, FERRARI, R, FOX, N. C

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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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Testing an aetiological model of visual hallucinations in Parkinson's disease von Gallagher, David A., Parkkinen, Laura, O'Sullivan, Sean S., Spratt, Alexander, Shah, Ameet, Davey, Clare C., Bremner, Fion D., Revesz, Tamas, Williams, David R., Lees, Andrew J., Schrag, Anette

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Neuropathological features of multiple system atrophy with cognitive impairment von Asi, Y. T., Ling, Helen, Ahmed, Z., Lees, A. J., Revesz, T., Holton, J. L.

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9.4 T MR microscopy of the substantia nigra with pathological validation in controls and disease von Massey, L A, Miranda, M A, Al-Helli, O, Parkes, H G, Thornton, J S, So, P-W, White, M J, Mancini, L, Strand, C, Holton, J, Lees, A J, Revesz, T, Yousry, T A

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PINK1 protein in normal human brain and Parkinson's disease von Gandhi, S., Muqit, M. M. K., Stanyer, L., Healy, D. G., Abou-Sleiman, P. M., Hargreaves, I., Heales, S., Ganguly, M., Parsons, L., Lees, A. J., Latchman, D. S., Holton, J. L., Wood, N. W., Revesz, T.

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Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant von Ling, H., de Silva, R., Massey, L. A., Courtney, R., Hondhamuni, G., Bajaj, N., Lowe, J., Holton, J. L., Lees, A., Revesz, T.

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Patterns of levodopa response in Parkinson's disease: a clinico-pathological study von Kempster, P. A., Williams, D. R., Selikhova, M., Holton, J., Revesz, T., Lees, A. J.

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Risk factors for symptomatic venous thromboembolism during therapy for childhood acute lymphoblastic leukemia von Mateos, M.K., Trahair, T.N., Mayoh, C., Barbaro, P.M., Sutton, R., Revesz, T., Barbaric, D., Giles, J.E., Alvaro, F., Mechinaud, F., Catchpoole, D., Kotecha, R.S., Dalla-Pozza, L., Quinn, M.C.J., MacGregor, S., Chenevix-Trench, G., Marshall, G.M.

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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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Foix–Chavany–Marie syndrome due to type E TDP43 pathology von Clark, C. N., Quaegebeur, A., Nirmalananthan, N., MacKinnon, A. D., Revesz, T., Holton, J. L., Bridges, L. R., Pereira, A. C.

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