Motor neurone disease

Por Talbot, K
Publicado em 2002

Amyotrophic lateral sclerosis, 2nd edn

Por Talbot, K
Publicado em 2007

Efficient insertion from an internal long terminal repeat (LTR)-LTR sequence on a reticuloendotheliosis virus vector is imprecise and cell specific.

Por Panganiban, A T, Talbot, K J
Publicado em 1993

The clinical landscape for SMA in a new therapeutic era

Por Talbot, K, Tizzano, E F
Publicado no Gene Ther (2017)

Spleen necrosis virus gag polyprotein is necessary for particle assembly and release but not for proteolytic processing.

Por Weaver, T A, Talbot, K J, Panganiban, A T
Publicado em 1990

Combined electro-acoustic stimulation: a beneficial union?

Por Talbot, K.N., Hartley, D.E.H.
Publicado em 2008

Molecular genetics of autosomal recessive spinal muscular atrophy.

Por Rodrigues, N. R., Talbot, K., Davies, K. E.
Publicado em 1996

Two outbreaks of Flavobacterium meningosepticum type E in a neonatal intensive care unit.

Por Hazuka, B T, Dajani, A S, Talbot, K, Keen, B M
Publicado em 1977

Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophy.

Por Talbot, K, Rodrigues, N, Bernert, G, Bittner, R, Davies, K
Publicado em 1996

Catastrophic hyperkalaemia following administration of suxamethonium chloride to a patient with undiagnosed amyotrophic lateral sclerosis

Por Turner, MR, Lawrence, H, Arnold, I, Ansorge, O, Talbot, K
Publicado no Clin Med (Lond) (2011)

The mRNA and RNA-copy pseudogenes encoding TM30nm, a human cytoskeletal tropomyosin.

Por MacLeod, A R, Houlker, C, Reinach, F C, Talbot, K
Publicado em 1986

The two-year progression of structural and functional cerebral MRI in amyotrophic lateral sclerosis

Por Menke, R.A.L., Proudfoot, M., Talbot, K., Turner, M.R.
Publicado no Neuroimage Clin (2017)

Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis

Por Filippini, N., Douaud, G., Mackay, C.E., Knight, S., Talbot, K., Turner, M.R.
Publicado em 2010

Budd-Chiari syndrome in association with polycystic disease of the liver and kidneys.

Por Bhupalan, A, Talbot, K, Forbes, A, Owen, M, Samson, D, Murray-Lyon, I M
Publicado em 1992

Gene deletions in spinal muscular atrophy.

Por Rodrigues, N R, Owen, N, Talbot, K, Patel, S, Muntoni, F, Ignatius, J, Dubowitz, V, Davies, K E
Publicado em 1996

Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations [Image: see text]

Por Bäumer, D., Hilton, D., Paine, S.M.L., Turner, M.R., Lowe, J., Talbot, K., Ansorge, O.
Publicado em 2010

A muscle-type tropomyosin in human fibroblasts: evidence for expression by an alternative RNA splicing mechanism.

Por MacLeod, A R, Houlker, C, Reinach, F C, Smillie, L B, Talbot, K, Modi, G, Walsh, F S
Publicado em 1985

Neurobehavioral abnormalities in the dysbindin-1 mutant, sandy, on a C57BL/6J genetic background

Por Cox, M.M., Tucker, A.M., Tang, J., Talbot, K., Richer, D.C., Yeh, L., Arnold, S.E.
Publicado em 2009

Thrombolysis by chemically modified coagulation factor Xa

Por Pryzdial, E. L. G., Meixner, S. C., Talbot, K., Eltringham-Smith, L. J., Baylis, J. R., Lee, F. M. H., Kastrup, C. J., Sheffield, W. P.
Publicado no J Thromb Haemost (2016)