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 2015

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 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 2013

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 2016

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

por 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.
Publicado 2020

Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss

por Vona, B., Schwartzbaum, D.A., Rodriguez, A.A., Lewis, S.S., Toosi, M.B., Radhakrishnan, P., Bozan, N., Akın, R., Doosti, M., Manju, R., Duman, D., Sineni, C.J., Nampoothiri, S., Karimiani, E.G., Houlden, H., Bademci, G., Tekin, M., Girisha, K.M., Maroofian, R., Douzgou, S.
Publicado 2022

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

por 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.
Publicado 2018

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

por 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.
Publicado 2019