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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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Published in Blood (01.03.2002)
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Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy
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
Published in American journal of medical genetics (15.08.2002)
Published in American journal of medical genetics (15.08.2002)
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Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease
Lohse, P, Maas, S, Lohse, P, Elleder, M, Kirk, J M, Besley, G T, Seidel, D
Published in Journal of lipid research (01.01.2000)
Published in Journal of lipid research (01.01.2000)
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