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29篇 您的检索式：作者名="Goodman SI"

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	题名	作者	年代	出处	被引量
1	Glutaric aciduria:a ‘ new' inborn error of amino acid metabolism显示文摘	Goodman SI Moe PG Markey SP	1974	Am J Hum Genet1974，26，：	1
2	Critical appraisal of ceftaroline in the management of community-acquired bacterial pneumonia and skin infections 显示文摘	Goodman JJ Martin SI	2012	Ther Clin Risk Manag2012，8，：	1
3	A molecular perspective on mammalian evolution from the gene encoding interphotoreceptor retinoid binding protein显示文摘	Stanhope M J Czelusniak J Si J-S Nickerson J Goodman M	1992	Mol Phylog Evol1992，1，：	1
4	IGF-1 and bFGF reduce glutaric acid and 3-hydroxyglutaric acid toxicity in striatal cultures显示文摘	Bjugstad KB Zawada WM Goodman SI	2001	J Inherit Metab Dis2001，24，6：	1
5	Glutaric acidemia type Ⅱ:heterogeneity of clinical and biochemical phenotypes显示文摘	Loehr JP Goodman SI Frurman FE	1990	Pediatr Res1990，27，：	1
6	Binding, hydration, and decarboxylation of the reaction intermediate glutaconyl-coenzyme A by human glutaryl-CoA dehydrogenase显示文摘	Westover JB Goodman SI Frerman FE	2001	Biochemistry2001，40，14：	1
7	Glutaric aciduria:A 'new' di-sorder of amino acid metabolism显示文摘	Goodman SI Markey SP Moe PG	1975	Biochem Med1975，12，1：	1
8	Glutaryl-CoA dehydrogenase deficiency and newborn screening:Retrospective analysis of a low excretor provides further evidence that some cases may be missed显示文摘	Gallagher RC Cowan TM Goodman SI	2005	Mol Genet Metab2005，86，3：	1
9	Molecular cloningand expression of a cDNA encoding human electron transferflavoprotein:ubiquinone oxidoreductase显示文摘	Goodman SI Axtell KM Bindoff LA	1994	Eur J Biochem1994，219，：	1
10	Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblasts显示文摘	Frerman FE Goodman SI		0，，01：	1
11	Glutaric aciduria; a 'new' disorder of amino acid metabolism显示文摘	Goodman SI Markey SP Moe PG	1975	Biochem Med1975，12，1：	1
12	Cloning of glutaryl- CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli显示文摘	Goodman SI Kratz IrE DiGiulio KA	1995	Hum Mol Genet1995，4，9：	1
13	Deficiency of electron transfer flavo- protein or electron transfer flavoprotein: ubiquinone oxidoreduc- tase in glutarie acidemia type II fibroblasts 显示文摘	Frerman FE Goodman SI	1985	Proc Natl Aead Sci U S A1985，82，13：	1
14	Glutaric aciduria:a 'new' disorder of amino acid metabolism显示文摘	Goodman SI Markey SP Moe PG	1975	Biochem Med1975，12，：	1
15	Glutaric aciduria; a 'new' disorder of amino acid metabolism 显示文摘	Goodman SI Markey SP Moe PG Miles BS Teng CC	1975	Biochem Med1975，12，1：	1
16	Glutaric academia type Ⅱ:heterogeneity of clinical and biochemical phenotypes显示文摘	Loehr JP Goodman SI Frerman FE		0，，：	1
17	Glutaryl-CoA dehydrogenase deficiency and newborn screening:retrospective analysis of a low excretor provides futher evidence that some cases may be missed显示文摘	Gallagher RC Cowan TM Goodman SI	2006	Mol Genet Metab2006，86，：	1
18	Glutaric aciduria; a“new” disorder of amino acid metabolism 显示文摘	Goodman SI Markey SP Moe PG	1975	Biochem Med1975，12，1：	1
19	Glyceroluria, psychomotor retardation, spasticity, dystrophic myopathy, and osteoporosis in sibship显示文摘	McCabe ERB Guggenheim MA Fennessey PV O'Brien D Miles BS Goodman SI	1977	Pediair Res1977，11，4：	1
20	Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type Ⅰ):review and report of thirty novel mutations显示文摘	Goodman SI Stein DE Schlesinger S	1998	Hum Murat1998，12，：	1

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