Apolipoprotein E4 and traumatic brain injury

מאת Houlden, H, Greenwood, R
יצא לאור 2006

Next generation sequencing in neuromuscular diseases

מאת Efthymiou, S, Manole, A, Houlden, H
הוצא לאור ב Curr Opin Neurol (2016)

Genotypic and phenotypic heterogeneity in familial microcoria

מאת Bremner, F D, Houlden, H, Smith, S E
יצא לאור 2004

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

מאת Arber, C. E., Li, A., Houlden, H., Wray, S.
הוצא לאור ב Neuropathol Appl Neurobiol (2015)

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

מאת King, A, Houlden, H, Hardy, J, Lane, R, Chancellor, A, de Belleroche, J
יצא לאור 1993

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

מאת Lee, M, Nelson, I, Houlden, H, Sweeney, M, Hilton-Jones, D, Blake, J, Wood, N, Reilly, M
יצא לאור 2002

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

מאת Houlden, H., Schneider, S. A., Paudel, R., Melchers, A., Schwingenschuh, P., Edwards, M., Hardy, J., Bhatia, K. P.
יצא לאור 2010

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

מאת Paudel, R., Li, A., Wiethoff, S., Bandopadhyay, R., Bhatia, K., de Silva, R., Houlden, H., Holton, J. L.
הוצא לאור ב Acta Neuropathol Commun (2015)

Genome-wide estimate of the heritability of Multiple System Atrophy

מאת Federoff, M, Price, TR, Sailer, A, Scholz, S, Hernandez, D, Nicolas, A, Singleton, AB, Nalls, M, Houlden, H
הוצא לאור ב Parkinsonism Relat Disord (2015)

Pantothenate kinase-associated neurodegeneration is not a synucleinopathy

מאת Li, A, Paudel, R, Johnson, R, Courtney, R, Lees, A J, Holton, J L, Hardy, J, Revesz, T, Houlden, H
יצא לאור 2013

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

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

GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY

מאת 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
יצא לאור 2009

Neuroimaging Features of Neurodegeneration with Brain Iron Accumulation

מאת Kruer, M.C., Boddaert, N., Schneider, S.A., Houlden, H., Bhatia, K.P., Gregory, A., Anderson, J.C., Rooney, W.D., Hogarth, P., Hayflick, S.J.
הוצא לאור ב AJNR Am J Neuroradiol (2012)

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

מאת 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
הוצא לאור ב Mol Psychiatry (2016)

Mutation in RNF170 causes sensory ataxic neuropathy with vestibular areflexia: a CANVAS mimic

מאת Cortese, A, Callegari, I., Curro, R., Vegezzi, E., Colnaghi, S., Versino, M., Alfonsi, E., Cosentino, G., Valente, EM., Gana, S., Tassorelli, C., Pichiecchio, A, Rossor, AM., Bugiardini, E., Biroli, A., Di Capua, D., Houlden, H., Reilly, MM
הוצא לאור ב J Neurol Neurosurg Psychiatry (2020)

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

מאת 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.
יצא לאור 2011

Baseline factors associated with early and late death in intracerebral haemorrhage survivors

מאת Banerjee, G., Ambler, G., Wilson, D., Hostettler, I. C., Shakeshaft, C., Lunawat, S., Cohen, H., Yousry, T., Al‐Shahi Salman, R., Lip, G. Y. H., Houlden, H., Muir, K. W., Brown, M. M., Jäger, H. R., Werring, D. J.
הוצא לאור ב Eur J Neurol (2020)

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

מאת 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.
יצא לאור 2012

Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series

מאת Koriath, C., Kenny, J., Adamson, G., Druyeh, R., Taylor, W., Beck, J., Quinn, L., Mok, T. H., Dimitriadis, A., Norsworthy, P., Bass, N., Carter, J., Walker, Z., Kipps, C., Coulthard, E., Polke, J. M., Bernal-Quiros, M., Denning, N., Thomas, R., Raybould, R., Williams, J., Mummery, C. J., Wild, E. J., Houlden, H., Tabrizi, S. J., Rossor, M. N., Hummerich, H., Warren, J. D., Rowe, J. B., Rohrer, J. D., Schott, J. M., Fox, N. C., Collinge, J., Mead, S.
הוצא לאור ב Mol Psychiatry (2018)

Genetic and phenotypic characterization of NKX6‐2‐related spastic ataxia and hypomyelination

מאת Chelban, V., Alsagob, M., Kloth, K., Chirita‐Emandi, A., Vandrovcova, J., Maroofian, R., Davagnanam, I., Bakhtiari, S., AlSayed, M. D., Rahbeeni, Z., AlZaidan, H., Malintan, N. T., Johannsen, J., Efthymiou, S., Ghayoor Karimiani, E., Mankad, K., Al‐Shahrani, S. A., Beiraghi Toosi, M., AlShammari, M., Groppa, S., Haridy, N. A., AlQuait, L., Qari, A., Huma, R., Salih, M. A., Almass, R., Almutairi, F. B., Hamad, M. H., Alorainy, I. A., Ramzan, K., Imtiaz, F., Puiu, M., Kruer, M. C., Bierhals, T., Wood, N. W., Colak, D., Houlden, H., Kaya, N.
הוצא לאור ב Eur J Neurol (2019)