PSEUDODOMINANT INHERITANCE OF SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY von TERRACCIANO, A, FOULDS, N. C, DITCHFIELD, A, BUNYAN, D. J, CROLLA, J. A, HUANG, S, SANTORELLI, F. M, HAMMANS, S. R

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Calpainopathy presenting as foot drop in a 41 year old von Burke, G, Hillier, C, Cole, J, Sampson, M, Bridges, L, Bushby, K, Barresi, R, Hammans, S.R

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Allgrove or 4 “A” syndrome: an autosomal recessive syndrome causing multisystem neurological disease von Kimber, J, McLean, B N, Prevett, M, Hammans, S R

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Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples von Hammans, S.R., Sweeney, M.G., Brockington, M., Morgan-Hughes, J.A., Harding, A.E.

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A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathy von Hammans, S R, Robinson, D O, Moutou, C, Kennedy, C R, Dennis, N R, Hughes, P J, Ellison, D W

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The sodium channel syndromes: expanding the phenotype associated with SCN4A mutations von Davies, N.P, Sutton, I, Winer, J.B, Moorcroft, P, Pall, H.S, Cole, T, Davies, M.B, Valente, E.M, Brancati, F, Hammans, S.R, Hanna, M.G

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Mitochondrial DNA mutation underlying Leigh's syndrome: Clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsy von Sweeney, M.G., Hammans, S.R., Duchen, L.W., Cooper, J.M., Schapira, A.H.V., Kennedy, C.R., Jacobs, J.M., Youl, B.D., Morgan-Hughes, J.A., Harding, A.E.

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Evidence for intramitochondrial complementation between deleted and normal mitochondrial DNA in some patients with mitochondrial myopathy von Hammans, S.R., Sweeney, M.G., Holt, I.J., Cooper, J.M., Toscano, A., Clark, J.B., Morgan-Hughes, J.A., Harding, A.E.

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