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Neuromuscular Disorders : NMD|March 1, 1993
Sarcolemmal distribution of abnormal dystrophin in Xp21 carriersM Vainzof, L V Nicholson, D E Bulman, et al.Journal of Medical Genetics|December 1, 1992
Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frameL V Nicholson, K M Bushby, M A Johnson, et al.Journal of the Neurological Sciences|February 1, 1992
A homologue of dystrophin is expressed at the blood vessel membrane of DMD and BMD patients: immunological evidenceN Augier, J Boucraut, J Léger, et al.Australian Veterinary Journal|January 20, 2016
Surgical implantation of temperature-sensitive transmitters and data-loggers to record body temperature in koalas (Phascolarctos cinereus)D Adam, S D Johnston, L Beard, et al.Neuromuscular Disorders : NMD|January 1, 1991
Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminusM J Cullen, J Walsh, L V Nicholson, et al.Journal of the Neurological Sciences|December 1, 1989
Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophyL V Nicholson, K Davison, M A Johnson, et al.Journal of Medical Genetics|August 1, 1992
Investigation of a female manifesting Becker muscular dystrophyI A Glass, L V Nicholson, E Watkiss, et al.The Journal of Clinical Investigation|February 1, 1992
Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?D Récan, P Chafey, F Leturcq, et al.Human Genetics|December 1, 1991
Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophyK M Bushby, N J Cleghorn, A Curtis, et al.Journal of Neurology|February 1, 1993
The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalitiesK M Bushby, D Gardner-Medwin, L V Nicholson, et al.Pageof 8