3 results for author:"Burin M.G." in Literature citations
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| Comparison between the biochemical properties of plasma chitotriosidase from normal individuals and from patients with Gaucher disease, GM1-gangliosidosis, Krabbe disease and heterozygotes for Gaucher disease. Wajner A., Michelin K., Burin M.G., Pires R.F., Pereira M.L., Giugliani R., Coelho J.C. Clin. Biochem. 40:365-369(2007) · Mapped (3) |
| Mucopolysaccharidosis type VI: Identification of novel mutations on the arylsulphatase B gene in South American patients. Petry M.F., Nonemacher K., Sebben J.C., Schwartz I.V., Azevedo A.C., Burin M.G., de Rezende A.R., Kim C.A., Giugliani R., Leistner-Segal S. J. Inherit. Metab. Dis. 28:1027-1034(2005) · Mapped (2) |
| Mucopolysaccharidosis VII: clinical, biochemical and molecular investigation of a Brazilian family. Schwartz I., Silva L.R., Leistner S., Todeschini L.A., Burin M.G., Pina-Neto J.M., Islam R.M., Shah G.N., Sly W.S., Giugliani R. Clin. Genet. 64:172-175(2003) · UniProtKB (1) |