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10篇 您的检索式:作者名="Matem D"
    题名 作者 年代 出处 被引量
1Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders 显示文摘Shell J J Matem D Millington D S 2000Inherit Metab Dis2000,23,1:1
2Molecular genetic analysis of 40 patients with glycogen storage disease type la: 100% mutation detection rateand 5 novel mutations显示文摘Seydewitz HH Matem D 2000Hum Murat2000,15,:1
3Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency 显示文摘Matem D Schehata BM Shekhawa P 2001Mol Genet Metab2001,72,:1
4Biosynthesis of coumarins显示文摘Matem U Kreusch D 1999Comprechensive Natural Products Chemistry1999,1,1:1
5Influence ofdietary fatty acid chain - length on metabolic tolerance inmouse models of inherited defects in mitochondrial fattyacid beta - oxidation 显示文摘Schuler A M Gower B A Matem D 2004Mol Genet Metab2004,83,4:1
6Molecular cloning, induction, and taxonomic distribution of caffeoyl-CoA 3-Omethyltransferase, an enzyme involved in disease resistance显示文摘Schmitt D Pakusch A E Matem U 1991J Biol Chem1991,,17:1
7Acute fatty liver of pregnancy associated with short-chain acyl-coezyme a dehydrogenase defieiency 显示文摘Matem D Hart P Murtha AP 2001J Pediat2001,138,4:1
8Newborn screening for lysosomal storage disorders 显示文摘Matem D Gavrilov D Oqlesbee D 2015Semin Perinatol2015,39,3:1
9Inhibition of phytosterol biosynthesis in elicitor-treated cultures of Ammimajus显示文摘Fulton D C Kroon P A Matem U 1993Phytochemistry1993,34,:1
10Type I glycogen storage dis-eases :disorders of the glucose-6-phosphatase complex 显示文摘Chou J Matem D Mansfield B 2002Curr MolMed2002,2,2:1
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