Brain transplantation--still fantasy? Discussion paper.

gan Morrison, K E
Cyhoeddwyd 1987

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

gan Morrison, K E, Mariyama, M, Yang-Feng, T L, Reeders, S T
Cyhoeddwyd 1991

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

gan Aceves, J., Mariscal, S., Morrison, K. E., Young, J. M.
Cyhoeddwyd 1985

Brexanolone for the treatment of patients with postpartum depression

gan Morrison, K.E., Cole, A.B., Thompson, S.M., Bale, T.L.
Cyhoeddwyd yn Drugs Today (Barc) (2019)

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

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

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

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

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

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

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

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

Prenatal prediction of spinal muscular atrophy.

gan 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
Cyhoeddwyd 1992

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

gan 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
Cyhoeddwyd 2009

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

gan 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
Cyhoeddwyd 1995

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

gan 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.
Cyhoeddwyd 2009

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

gan 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.
Cyhoeddwyd yn Neurobiol Aging (2016)