Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease

Por Jacquemont, M, Campion, D, Hahn, V, Tallaksen, C, Frebourg, T, Brice, A, Durr, A
Publicado em 2002

Spastin mutations are frequent in sporadic spastic paraparesis and their spectrum is different from that observed in familial cases

Por Depienne, C, Tallaksen, C, Lephay, J Y, Bricka, B, Poea‐Guyon, S, Fontaine, B, Labauge, P, Brice, A, Durr, A
Publicado em 2006

An up-date on health-related quality of life in myasthenia gravis -results from population based cohorts

Por Boldingh, M. I., Dekker, L., Maniaol, A. H., Brunborg, C., Lipka, A. F., Niks, E. H., Verschuuren, J. J. G. M., Tallaksen, C. M. E.
Publicado no Health Qual Life Outcomes (2015)

Multi-system neurological disease is common in patients with OPA1 mutations

Por Yu-Wai-Man, P., Griffiths, P.G., Gorman, G.S., Lourenco, C.M., Wright, A.F., Auer-Grumbach, M., Toscano, A., Musumeci, O., Valentino, M.L., Caporali, L., Lamperti, C., Tallaksen, C.M., Duffey, P., Miller, J., Whittaker, R.G., Baker, M.R., Jackson, M.J., Clarke, M.P., Dhillon, B., Czermin, B., Stewart, J.D., Hudson, G., Reynier, P., Bonneau, D., Marques, W., Lenaers, G., McFarland, R., Taylor, R.W., Turnbull, D.M., Votruba, M., Zeviani, M., Carelli, V., Bindoff, L.A., Horvath, R., Amati-Bonneau, P., Chinnery, P.F.
Publicado em 2010