Retrovirally mediated correction of bone marrow–derived mesenchymal stem cells from patients with mucopolysaccharidosis type I von Baxter, Melissa A., Wynn, Robert F., Deakin, Jonathan A., Bellantuono, Ilaria, Edington, Kirsten G., Cooper, Alan, Besley, Guy T.N., Church, Heather J., Wraith, J. Ed, Carr, Trevor F., Fairbairn, Leslie J.

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Novel OCTN2 mutations: No genotype-phenotype correlations: Early carnitine therapy prevents cardiomyopathy von Lamhonwah, Anne-Marie, Olpin, Simon E., Pollitt, Rodney J., Vianey-Saban, Christine, Divry, Priscille, Guffon, Nathalie, Besley, Guy T. N., Onizuka, Russell, De Meirleir, Linda J., Cvitanovic-Sojat, Ljerka, Baric, Ivo, Dionisi-Vici, Carlo, Fumic, Ksenija, Maradin, Miljenka, Tein, Ingrid

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Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease von Lohse, P, Maas, S, Lohse, P, Elleder, M, Kirk, J M, Besley, G T, Seidel, D

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Five cases of isolated glycerol kinase deficiency, including two families: failure to find genotype:phenotype correlation von Sargent, Carole A, Kidd, Alexa, Moore, Sue, Dean, John, Besley, Guy T N, Affara, Nabeel A

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Prenatal Diagnosis of Inborn Errors of Metabolism von Besley, Guy T. N.

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Acknowledgements von Roels, Frank, De Bie, Sylvia, Schutgens, Ruud B. H., Besley, Guy T. N.

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Acknowledgements von Roels, Frank, De Bie, Sylvia, Schutgens, Ruud B. H., Besley, Guy T. N.

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Diagnosis of human peroxisomal disorders. A handbook von ROELS, Franck, DE BIE, Sylvia, SCHUTGENS, Ruud B. H, BESLEY, Guy T. N, GOLDFISCHER, Sidney

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Evidence from lectin-binding studies for abnormal glycosylation ofβ-hexosaminidase in the leukaemic cell-line CCRF/CEM von Moss, Stephen E, Besley, Guy T N

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Lysosomal Storage Diseases. Biochemical and Clinical Aspects. By Richard W. E. Watts and Dorothy A. Gibbs. London: Taylor & Francis, 1968, 284 pages, £35, ISBN 0 85066 326 1 von Besley, Guy T. N.

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Genetic Biochemical Disorder. By Philip F. Benson and Anthony H. Fensom. Oxford: Oxford University Press. 1985. 692 pages. £55. ISBN 0 19 261193 3 von Besley, Guy T. N.

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Book reviews von Besley, Guy T. N.

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Lysosomal Storage Diseases. Biochemical and Clinical Aspects. By WattsRichard W. E. and GibbsDorothy A.. London: Taylor & Francis, 1968, 284 pages, £35, ISBN 0 85066 326 1 von Besley, Guy T. N.

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Book Reviews von Besley, Guy T. N.

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Genetic Biochemical Disorder. By BensonPhilip F. and FensomAnthony H.. Oxford: Oxford University Press. 1985. 692 pages. £55. ISBN 0 19 261193 3 von Besley, Guy T. N.

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Amylo-1,6-glucosidase activity in cultured cells: A deficiency in type III glycogenosis with prenatal studies von Besley, Guy T. N., Cohen, Patricia T. W., Faed, Michael J. W., Wolstenholme, John

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Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene von Jansen, Gerbert A, Oftnan, Rob, Ferdinandusse, Sacha, Ijlst, Lodewijk, Muijsers, Anton O, Skjeldal, Ola H, Stokke, Oddvar, Jakobs, Cornells, Besley, Guy T.N, Wraith, J. Ed, Wanders, Ronald J.A

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Twenty-two novel mutations in the lysosomal α-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II von Hermans, Monique M.P., Leenen, Dik van, Kroos, Marian A., Beesley, Clare E., Van der Ploeg, Ans T., Sakuraba, Hitoshi, Wevers, Ron, Kleijer, Wim, Michelakakis, Helen, Kirk, Edwin P., Fletcher, Janice, Bosshard, Nils, Basel-Vanagaite, Lina, Besley, Guy, Reuser, Arnold J.J.

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Ornithine aminotransferase deficiency: Diagnostic difficulties in neonatal presentation von Cleary, M. A., Dorland, L., Koning, T. J., Poll‐The, B. T., Duran, M., Mandell, R., Shih, V. E., Berger, R., Olpin, S. E., Besley, G. T. N.

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Relationship of Octanoylcarnitine Concentrations to Age at Sampling in Unaffected Newborns Screened for Medium-Chain Acyl-CoA Dehydrogenase Deficiency von KHALID, Javaria M, OERTON, Juliet, DEZATEUX, Carol, BESLEY, Guy, DALTON, Neil, DOWNING, Melanie, GREEN, Anne, HENDERSON, Mick, KRYWAWYCH, Steve, WILEY, Veronica, WILCKEN, Bridget

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