Enterovirus related metabolic myopathy: a postviral fatigue syndrome von Lane, R J M, Soteriou, B A, Zhang, H, Archard, L C

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Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease von Orrell, R W, Lane, R J M, Ross, M

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Cytochrome c Oxidase Deficiency Associated with the First Stop-Codon Point Mutation in Human mtDNA von Hanna, M.G., Nelson, I.P., Rahman, S., Lane, R.J.M., Land, J., Heales, S., Cooper, M.J., Schapira, A.H.V., Morgan-Hughes, J.A., Wood, N.W.

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Phenotypic variability in siblings with type III spinal muscular atrophy von Muqit, M M K, Moss, J, Sewry, C, Lane, R J M

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Transient myasthenia gravis in an elderly woman von Wong, W W Y, Lane, R J M

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Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotr... von Orrell, R W, Habgood, J J, Gardiner, I, King, A W, Bowe, F A, Hallewell, R A, Marklund, S L, Greenwood, J, Lane, R J.M, deBelleroche, J

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Muscle fibre characteristics and lactate responses to exercise in chronic fatigue syndrome von Lane, Russell J M, Barrett, Michael C, Woodrow, David, Moss, Jill, Fletcher, Robert, Archard, Leonard C

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Clinical characteristics of SOD1 gene mutations in UK families with ALS von Orrell, Richard W, Habgood, James J, Malaspina, Andrea, Mitchell, John, Greenwood, Juliet, Lane, Russell J.M, deBelleroche, Jackie S

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The long and winding road: the journey taken by headache sufferers in search of help von Davies, PTG, Lane, RJM, Astbury, T, Fontebasso, M, Murphy, J, Matharu, M

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Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles von Orrell, R W, King, A W, Hilton, D A, Campbell, M J, Lane, R J, de Belleroche, J S

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Clinical features and management of two cases of encephalitis lethargica von Blunt, Stavia B., Lane, Russel J. M., Turjanski, Nora, Perkin, G. David

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Drug-induced neurological disorders von Lane, R J, Routledge, P A

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Oculomotor function in amyotrophic lateral sclerosis: Evidence for frontal impairment von Shaunak, S., Orrell, R. W., O'Sullivan, E., Hawken, M. B., Lane, R. J. M., Henderson, L., Kennard, C.

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Familial cramp due to potassium-aggravated myotonia von Orrell, Richard W, Jurkat-Rott, Karin, Lehmann-Horn, Frank, Lane, Russell J M

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Heterogeneity in chronic fatigue syndrome: evidence from magnetic resonance spectroscopy of muscle von Lane, Russell J.M, Barrett, Michael C, Taylor, Doris J, Kemp, Graham J, Lodi, Raffaele

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Recurrent coital amnesia von LANE, RUSSELL J M

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The relationship of spinal muscular atrophy to motor neuron disease : Investigation of SMN and NAIP gene deletions in sporadic and familial ALS von ORRELL, R. W, HABGOOD, J. J, DE BELLEROCHE, J. S, LANE, R. J. M

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Clinical trials of riluzole in patients with ALS von Miller, R. G., Bouchard, J. P., Duquette, P., Eisen, A., Gelinas, D., Harati, Y., Munsat, T. L., Powe, L., Rothstein, J., Salzman, P., Sufit, R. L.

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Persistence of enteroviral RNA in chronic fatigue syndrome is associated with the abnormal production of equal amounts of positive and negative strands of enteroviral RNA von Cunningham, Louise, Bowles, N. E, Lane, R. J. M, Dubowitz, V, Archard, L. C

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Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis von Orell, Richard W., Habgood, James, Rudge, Petter, Lane, Russell J. M., de Belleroche, Jackie S.

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