6 results for author:"Engelke U.F." in Literature citations
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| Mitochondrial involvement and erythronic acid as a novel biomarker in transaldolase deficiency. Engelke U.F., Zijlstra F.S., Mochel F., Valayannopoulos V., Rabier D., Kluijtmans L.A., Perl A., Verhoeven-Duif N.M., de Lonlay P., Wamelink M.M. et al. Biochim. Biophys. Acta 1802:1028-1035(2010) · Mapped (4) |
| Free sialic acid storage disease without sialuria. Mochel F., Yang B., Barritault J., Thompson J.N., Engelke U.F., McNeill N.H., Benko W.S., Kaneski C.R., Adams D.R., Tsokos M. et al. Ann. Neurol. 65:753-757(2009) · Mapped (4) |
| Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluids. Engelke U.F., Tassini M., Hayek J., de Vries M., Bilos A., Vivi A., Valensin G., Buoni S., Zannolli R., Brussel W. et al. NMR Biomed 22:538-544(2009) · Mapped (2) |
| Aminoacylase I deficiency: a novel inborn error of metabolism. Van Coster R.N., Gerlo E.A., Giardina T.G., Engelke U.F., Smet J.E., De Praeter C.M., Meersschaut V.A., De Meirleir L.J., Seneca S.H., Devreese B. et al. Biochem. Biophys. Res. Commun. 338:1322-1326(2005) · UniProtKB (1) · Mapped (4) |
| Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency. Binzak B.A., Wevers R.A., Moolenaar S.H., Lee Y.-M., Hwu W.-L., Poggi-Bach J., Engelke U.F.H., Hoard H.M., Vockley J.G., Vockley J. Am. J. Hum. Genet. 68:839-847(2001) · UniProtKB (1) |
| Defect in dimethylglycine dehydrogenase, a new inborn error of metabolism: NMR spectroscopy study. Moolenaar S.H., Poggi-Bach J., Engelke U.F.H., Corstiaensen J.M.B., Heerschap A., de Jong J.G.N., Binzak B.A., Vockley J., Wevers R.A. Clin. Chem. 45:459-464(1999) · UniProtKB (1) |