Brain transplantation--still fantasy? Discussion paper.

Por Morrison, K E
Publicado em 1987

Sequence and localization of a partial cDNA encoding the human alpha 3 chain of type IV collagen.

Por Morrison, K E, Mariyama, M, Yang-Feng, T L, Reeders, S T
Publicado em 1991

The binding of doxepin to histamine H1-receptors in guinea-pig and rat brain.

Por Aceves, J., Mariscal, S., Morrison, K. E., Young, J. M.
Publicado em 1985

High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.

Por Morrison, K E, Daniels, R J, Suthers, G K, Flynn, G A, Francis, M J, Buckle, V J, Davies, K E
Publicado em 1992

Establishing the UK DNA Bank for motor neuron disease (MND)

Por Smith, Lucy, Cupid, B. C., Dickie, B. G. M., Al-Chalabi, A., Morrison, K. E., Shaw, C. E., Shaw, P. J.
Publicado no BMC Genet (2015)

Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13.

Por Theodosiou, A. M., Morrison, K. E., Nesbit, A. M., Daniels, R. J., Campbell, L., Francis, M. J., Christodoulou, Z., Davies, K. E.
Publicado em 1994

Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's disease

Por Lewthwaite, A.J., Lambert, T.D., Rolfe, E.B., Olgiati, S., Quadri, M., Simons, E.J., Morrison, K.E., Bonifati, V., Nicholl, D.J.
Publicado no Parkinsonism Relat Disord (2015)

Prenatal prediction of spinal muscular atrophy.

Por Daniels, R J, Suthers, G K, Morrison, K E, Thomas, N H, Francis, M J, Mathew, C G, Loughlin, S, Heiberg, A, Wood, D, Dubowitz, V
Publicado em 1992

A mechanism for low penetrance in an ALS family with a novel SOD1 deletion

Por Zinman, L, Liu, H N., Sato, C, Wakutani, Y, Marvelle, A F., Moreno, D, Morrison, K E., Mohlke, K L., Bilbao, J, Robertson, J, Rogaeva, E
Publicado em 2009

Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele.

Por Daniels, R J, Campbell, L, Rodrigues, N R, Francis, M J, Morrison, K E, McLean, M, MacKenzie, A, Ignatius, J, Dubowitz, V, Davies, K E
Publicado em 1995

A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS

Por Wills, A -M., Cronin, S, Slowik, A, Kasperaviciute, D, Van Es, M A., Morahan, J M., Valdmanis, P N., Meininger, V, Melki, J, Shaw, C E., Rouleau, G A., Fisher, E M.C., Shaw, P J., Morrison, K E., Pamphlett, R, Van den Berg, L H., Figlewicz, D A., Andersen, P M., Al-Chalabi, A, Hardiman, O, Purcell, S, Landers, J E., Brown, R H.
Publicado em 2009

Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson’s disease: analysis of a large multi-center study

Por Wang, L., Heckman, M.G., Aasly, J. O., Annesi, G., Bozi, M., Chung, S. J., Clarke, C., Crosiers, D., Eckstein, G., Garraux, G., Hadjigeorgiou, G. M., Hattori, N., Jeon, B., Kim, Y. J., Kubo, M., Lesage, S., Lin, J. J., Lynch, T., Lichtner, P., Mellick, G. D., Mok, V., Morrison, K. E., Quattrone, A., Satake, W., Silburn, P. A., Stefanis, L., Stockton, J. D., Tan, E. K., Toda, T., Brice, A., Van Broeckhoven, C., Uitti, R. J., Wirdefeldt, K., Wszolek, Z., Xiromerisiou, G., Maraganore, D. M., Gasser, T., Kruger, R., Farrer, M. J., Ross, O. A., Sharma, M.
Publicado no Neurobiol Aging (2016)