Cerebral amyloidosis: amyloid subunits, mutants and phenotypes

Por Rostagno, A., Holton, J. L., Lashley, T., Revesz, T., Ghiso, J.
Publicado em 2009

The Significance of α-Synuclein, Amyloid-β and Tau Pathologies in Parkinson’s Disease Progression and Related Dementia

Por Compta, Y., Parkkinen, L., Kempster, P., Selikhova, M., Lashley, T., Holton, J.L., Lees, A.J., Revesz, T.
Publicado em 2013

Neuropathology of Beta-propeller protein associated neurodegeneration (BPAN): a new tauopathy

Por Paudel, R., Li, A., Wiethoff, S., Bandopadhyay, R., Bhatia, K., de Silva, R., Houlden, H., Holton, J. L.
Publicado no Acta Neuropathol Commun (2015)

Pantothenate kinase-associated neurodegeneration is not a synucleinopathy

Por Li, A, Paudel, R, Johnson, R, Courtney, R, Lees, A J, Holton, J L, Hardy, J, Revesz, T, Houlden, H
Publicado em 2013

Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant

Por Ling, H, de Silva, R, Massey, L A, Courtney, R, Hondhamuni, G, Bajaj, N, Lowe, J, Holton, J L, Lees, A, Revesz, T
Publicado no Neuropathol Appl Neurobiol (2014)

The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5 year retrospective study

Por Bennett, D L H, Groves, M, Blake, J, Holton, J L, King, R H M, Orrell, R W, Ginsberg, L, Reilly, M M
Publicado em 2008

Sodium and chloride channelopathies with myositis: coincidence or connection?

Por Matthews, E., Miller, J.A.L., Macleod, M.R., Ironside, J., Ambler, G., Labrum, R., Sud, R., Holton, J.L., Hanna, M.G.
Publicado em 2011

Expression of BRI2 mRNA and protein in normal human brain and familial British dementia: its relevance to the pathogenesis of disease

Por 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.
Publicado em 2008

Characterisation of a novel NR4A2 mutation in Parkinson’s disease brain

Por Sleiman, P.M.A., Healy, D.G., Muqit, M.M.K., Yang, Y.X., Van Der Brug, M., Holton, J.L., Revesz, T., Quinn, N.P., Bhatia, K., Diss, J.K.J., Lees, A.J., Cookson, M.R., Latchman, D.S., Wood, N.W.
Publicado no Neurosci Lett (2009)

Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient

Por McColgan, P., Viegas, S., Gandhi, S., Bull, K., Tudor, R., Sheikh, F., Pinney, J., Fontana, M., Rowczenio, D., Gillmore, J. D., Gilbertson, J. A., Whelan, C. J., Shah, S., Jaunmuktane, Z., Holton, J. L., Schott, J. M., Werring, D. J., Hawkins, P. N., Reilly, M. M.
Publicado no J Neurol (2014)

The α‐synuclein gene in multiple system atrophy

Por Ozawa, T, Healy, D G, Abou‐Sleiman, P M, Ahmadi, K R, Quinn, N, Lees, A J, Shaw, K, Wullner, U, Berciano, J, Moller, J C, Kamm, C, Burk, K, Josephs, K A, Barone, P, Tolosa, E, Goldstein, D B, Wenning, G, Geser, F, Holton, J L, Gasser, T, Revesz, T, Wood, N W
Publicado em 2006