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Lancet (London, England)|March 31, 1979
Carrier detection in Duchenne muscular dystrophy: Assessment of the effect of age on detection-rate with serum-creatine-kinase-activityG A Nicholson, D Gardner-Medwin, R J Pennington, et al.Journal of the Neurological Sciences|July 1, 1981
Carrier testing in families of isolated cases of duchenne muscular dystrophy. Creatine kinase activities in female relatives of mothers with normal CK activityG A Nicholson, R J Lane, D Gardner-Medwin, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1973
The syndrome of myosclerosisW G Bradley, P Hudgson, D Gardner-Medwin, et al.Journal of the Neurological Sciences|November 1, 1979
An evaluation of some carrier detection techniques in Duchenne muscular dystrophyR J Lane, P Maskrey, G A Nicholson, et al.International Rehabilitation Medicine|January 1, 1980
Rehabilitation in muscular dystrophyD Gardner-MedwinJournal of the Neurological Sciences|July 1, 1978
A genetic study of subacute and chronic spinal muscular atrophy in childhood. A nosological analysis of 124 index patientsJ Pearn, S Bundley, C O Carter, et al.Developmental Medicine and Child Neurology|January 1, 1992
Familial paroxysmal rhabdomyolysis: management of two cases of the non-exertional typeV Ramesh, D Gardner-MedwinBrain & Development|January 1, 1989
Some studies of the Duchenne and autosomal recessive types of muscular dystrophyD Gardner-Medwin, P SharplesNeuroradiology|January 1, 1978
CT scan appearances in Leigh's disease (subacute necrotizing encephalomyelopathy)K Hall, D Gardner-MedwinJournal of the Neurological Sciences|April 1, 1984
Severe muscular dystrophy in girlsD Gardner-Medwin, H M JohnstonPageof 20