High-risk childhood acute lymphoblastic leukemia in first remission treated with novel intensive chemotherapy and allogeneic transplantation von Marshall, G M, Dalla Pozza, L, Sutton, R, Ng, A, de Groot-Kruseman, H A, van der Velden, V H, Venn, N C, van den Berg, H, de Bont, E S J M, Maarten Egeler, R, Hoogerbrugge, P M, Kaspers, G J L, Bierings, M B, van der Schoot, E, van Dongen, J, Law, T, Cross, S, Mueller, H, de Haas, V, Haber, M, Révész, T, Alvaro, F, Suppiah, R, Norris, M D, Pieters, R

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Preemptive alloimmune intervention in high-risk pediatric acute lymphoblastic leukemia patients guided by minimal residual disease level before stem cell transplantation von Lankester, A C, Bierings, M B, van Wering, E R, Wijkhuijs, A J M, de Weger, R A, Wijnen, J T, Vossen, J M, Versluys, B, Egeler, R M, van Tol, M J D, Putter, H, Révész, T, van Dongen, J J M, van der Velden, V H J, Schilham, M W

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Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis von Göransdotter Ericson, Kim, Fadeel, Bengt, Nilsson-Ardnor, Sofie, Söderhäll, Cilla, Samuelsson, AnnaCarin, Janka, Gritta, Schneider, Marion, Gürgey, Aytemiz, Yalman, Nevin, Révész, Tom, Egeler, R. Maarten, Jahnukainen, Kirsi, Storm-Mathiesen, Ingebjörg, Haraldsson, Ásgeir, Poole, Janet, de Saint Basile, Geneviève, Nordenskjöld, Magnus, Henter, Jan-Inge

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A stop-codon mutation in the BRI gene associated with familial British dementia von Ghiso, Jorge, Vidal, Ruben, Frangione, Blas, Rostagno, Agueda, Mead, Simon, Révész, Tamas, Plant, Gordon

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Neuronal cytoskeletal changes are an early consequence of repetitive head injury von GEDDES, J. F, VOWLES, G. H, NICOLL, J. A. R, REVESZ, T

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Donor leukocyte infusion after hematopoietic stem cell transplantation in patients with juvenile myelomonocytic leukemia von YOSHIMI, A, BADER, P, KREMENS, B, SYKORA, K.-W, URBAN, C, HASLE, H, KORTHOF, E, REVESZ, T, FISCHER, A, NÖLIKE, P, LOCATELLI, F, NIEMEYER, C. M, MATTHES-MARTIN, S, STARY, J, SEDLACEK, P, DUFFNER, U, KLINGEBIEL, T, DILLOO, D, HOLTER, W, ZINTL, F

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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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How to improve the search for an unrelated haematopoietic stem cell donor. Faster is better than more von HEEMSKERK, M. B. A, VAN WALRAVEN, S. M, DONKER, A. E, HOOGERBRUGGE, P. M, VAN ROOD, J. J, CLAAS, F. H. J, OUDSHOORN, M, CORNELISSEN, J. J, BARGE, R. M. Y, BREDIUS, R. G. M, EGELER, R. M, LIE, Jlwtj, REVESZ, T, SINTNICOLAAS, K, WULFFRAAT, N. M

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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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Extramedullary infiltrates at diagnosis have no prognostic significance in children with acute myeloid leukaemia von BISSCHOP, M. M, REVESZ, T, BIERINGS, M, VAN WEERDEN, J. F, VAN WERING, E. R, HÄHLEN, K, VAN DER DOES-VAN DEN BERG, A

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Evidence for pathological involvement of the spinal cord in motor neuron disease-inclusion dementia von HOLTON, J. L, REVESZ, T, CROOKS, R, SCARAVILLI, F

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Sequence, genomic structure and tissue expression of Human BRI3, a member of the BRI gene family von Vidal, R, Calero, M, Révész, T, Plant, G, Ghiso, J, Frangione, B

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