Brain transplantation--still fantasy? Discussion paper.

per Morrison, K E
Publicat 1987

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

per Morrison, K E, Mariyama, M, Yang-Feng, T L, Reeders, S T
Publicat 1991

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

per Aceves, J., Mariscal, S., Morrison, K. E., Young, J. M.
Publicat 1985

Brexanolone for the treatment of patients with postpartum depression

per Morrison, K.E., Cole, A.B., Thompson, S.M., Bale, T.L.
Publicat a Drugs Today (Barc) (2019)

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

per Morrison, K E, Daniels, R J, Suthers, G K, Flynn, G A, Francis, M J, Buckle, V J, Davies, K E
Publicat 1992

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

per Smith, Lucy, Cupid, B. C., Dickie, B. G. M., Al-Chalabi, A., Morrison, K. E., Shaw, C. E., Shaw, P. J.
Publicat a BMC Genet (2015)

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

per Theodosiou, A. M., Morrison, K. E., Nesbit, A. M., Daniels, R. J., Campbell, L., Francis, M. J., Christodoulou, Z., Davies, K. E.
Publicat 1994

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

per Lewthwaite, A.J., Lambert, T.D., Rolfe, E.B., Olgiati, S., Quadri, M., Simons, E.J., Morrison, K.E., Bonifati, V., Nicholl, D.J.
Publicat a Parkinsonism Relat Disord (2015)

Prenatal prediction of spinal muscular atrophy.

per 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
Publicat 1992

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

per 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
Publicat 2009

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

per 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
Publicat 1995

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

per 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.
Publicat 2009

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

per 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.
Publicat a Neurobiol Aging (2016)