Brain transplantation--still fantasy? Discussion paper.

Yazar: Morrison, K E
Baskı/Yayın Bilgisi 1987

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

Yazar: Morrison, K E, Mariyama, M, Yang-Feng, T L, Reeders, S T
Baskı/Yayın Bilgisi 1991

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

Yazar: Aceves, J., Mariscal, S., Morrison, K. E., Young, J. M.
Baskı/Yayın Bilgisi 1985

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

Yazar: Morrison, K E, Daniels, R J, Suthers, G K, Flynn, G A, Francis, M J, Buckle, V J, Davies, K E
Baskı/Yayın Bilgisi 1992

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

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

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

Yazar: Theodosiou, A. M., Morrison, K. E., Nesbit, A. M., Daniels, R. J., Campbell, L., Francis, M. J., Christodoulou, Z., Davies, K. E.
Baskı/Yayın Bilgisi 1994

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

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

Prenatal prediction of spinal muscular atrophy.

Yazar: 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
Baskı/Yayın Bilgisi 1992

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

Yazar: 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
Baskı/Yayın Bilgisi 2009

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

Yazar: 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
Baskı/Yayın Bilgisi 1995

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

Yazar: 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.
Baskı/Yayın Bilgisi 2009

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

Yazar: 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.
Yayımlandı Neurobiol Aging (2016)