Authors: Hargreaves, IP Heales, SJR Olpin, SE Morgan-Hughes, JA Land, JM

Citation: Ip. Hargreaves et al., The diagnosis of carnitine palmitoyltransferase II deficiency is now possible in small skeletal muscle biopsies, J INH MET D, 23(4), 2000, pp. 352-354

Authors: Pulkes, T Siddiqui, A Morgan-Hughes, JA Hanna, MG

Citation: T. Pulkes et al., A novel mutation in the mitochondrial tRNA(Tyr) gene associated with exercise intolerance, NEUROLOGY, 55(8), 2000, pp. 1210-1212

Authors: Pulkes, T Eunson, L Patterson, V Siddiqui, A Wood, NW Nelson, IP Morgan-Hughes, JA Hanna, MG

Citation: T. Pulkes et al., The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS, ANN NEUROL, 46(6), 1999, pp. 916-919

Authors: Brett, M Persey, MR Reilly, MM Revesz, T Booth, DR Booth, SE Hawkins, PN Pepys, MB Morgan-Hughes, JA

Citation: M. Brett et al., Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis, BRAIN, 122, 1999, pp. 183-190

Authors: Morgan-Hughes, JA Hanna, MG

Citation: Ja. Morgan-hughes et Mg. Hanna, Mitochondrial encephalomyopathies: the enigma of genotype versus phenotype, BBA-BIOENER, 1410(2), 1999, pp. 125-145