Multiple mitochondrial DNA deletions in monozygotic twins with OPMD von Muqit, M M K, Larner, A J, Sweeney, M G, Sewry, C, Stinton, V J, Davis, M B, Healy, D G, Payne, S J, Chotai, K, Wood, N W, Lane, R J M

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Antioxidant treatment for amyotrophic lateral sclerosis or motor neuron disease von Orrell, Richard W, Lane, Russell JM, Ross, Mark, Orrell, Richard W

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PONM14 A novel homozygous missense mutation in the GNE gene of two brothers with hereditary inclusion body myopathy type 2 von Sheerin, U M, Lane, R J M, Rakowicz, W, Roncaroli, F

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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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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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Barraquer-Simons lipodystrophy, Raynaud's phenomenon and cutaneous vasculitis von Porter, W. M., O'Gorman-Lalor, O., Lane, R. J. M., Francis, N., Bunker, C. B.

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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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A diagnostic dilemma of intracranial pathology: coincidence or the result of cranial trauma? von Cartwright, Georgina, Bailey, B M W, Lane, R J M, Messiha, 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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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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Dermatomyositis in association with transitional cell carcinoma of the bladder von MALLON, E, OSBORNE, G, DINNEEN, M, LANE, R. J. M, GLASER, M, BUNKER, C. B

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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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Histological surprise: callosal tuberculoma presenting as malignant glioma von Fath-Ordoubadi, Farzin, Lane, Russell J M, Richards, Peter G

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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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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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Recurrent Epistaxes in Hereditary Haemorrhagic Telangiectasia von Lim, S M C, Lane, R J M

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

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