Apolipoprotein E4 and traumatic brain injury

Por Houlden, H, Greenwood, R
Publicado em 2006

Next generation sequencing in neuromuscular diseases

Por Efthymiou, S, Manole, A, Houlden, H
Publicado no Curr Opin Neurol (2016)

Genotypic and phenotypic heterogeneity in familial microcoria

Por Bremner, F D, Houlden, H, Smith, S E
Publicado em 2004

Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories

Por Arber, C. E., Li, A., Houlden, H., Wray, S.
Publicado no Neuropathol Appl Neurobiol (2015)

Absence of linkage between chromosome 21 loci and familial amyotrophic lateral sclerosis.

Por King, A, Houlden, H, Hardy, J, Lane, R, Chancellor, A, de Belleroche, J
Publicado em 1993

Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease

Por Lee, M, Nelson, I, Houlden, H, Sweeney, M, Hilton-Jones, D, Blake, J, Wood, N, Reilly, M
Publicado em 2002

THAP1 mutations (DYT6) are an additional cause of early-onset dystonia

Por Houlden, H., Schneider, S. A., Paudel, R., Melchers, A., Schwingenschuh, P., Edwards, M., Hardy, J., Bhatia, K. P.
Publicado em 2010

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)

Genome-wide estimate of the heritability of Multiple System Atrophy

Por Federoff, M, Price, TR, Sailer, A, Scholz, S, Hernandez, D, Nicolas, A, Singleton, AB, Nalls, M, Houlden, H
Publicado no Parkinsonism Relat Disord (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

Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series

Por van de Leemput, J, Wavrant-De Vrièze, F, Rafferty, I, Bras, JM, Giunti, P, Fisher, EMC, Hardy, J, Singleton, AB, Houlden, H
Publicado em 2010

GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY

Por Segarane, B, Li, A, Paudel, R, Scholz, S, Neumann, J, Lees, A, Revesz, T, Hardy, J, Mathias, C J., Wood, N W., Holton, J, Houlden, H
Publicado em 2009

Brain iron accumulation affects myelin-related molecular systems implicated in a rare neurogenetic disease family with neuropsychiatric features

Por Heidari, M, Johnstone, D M, Bassett, B, Graham, R M, Chua, A C G, House, M J, Collingwood, J F, Bettencourt, C, Houlden, H, Ryten, M, Olynyk, J K, Trinder, D, Milward, E A
Publicado no Mol Psychiatry (2016)

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations

Por Polke, J.M., Laurá, M., Pareyson, D., Taroni, F., Milani, M., Bergamin, G., Gibbons, V.S., Houlden, H., Chamley, S.C., Blake, J., DeVile, C., Sandford, R., Sweeney, M.G., Davis, M.B., Reilly, M.M.
Publicado em 2011

Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort

Por Davidson, G. L., Murphy, S. M., Polke, J. M., Laura, M., Salih, M. A. M., Muntoni, F., Blake, J., Brandner, S., Davies, N., Horvath, R., Price, S., Donaghy, M., Roberts, M., Foulds, N., Ramdharry, G., Soler, D., Lunn, M. P., Manji, H., Davis, M. B., Houlden, H., Reilly, M. M.
Publicado em 2012