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    1.3-methylglutaconic aciduria in a Chinese patient with glycogen storage disease Ib

    Law, LK, Tang, NLS,     More...

    JOURNAL OF INHERITED METABOLIC DISEASE[0141-8955], Published 2003, Volume 26, Issue 7, Pages 705-709

    收錄情况: WOS SCOPUS

    WOS核心合集引用: 11  2023影響因子:  4.2  发表年影響因子:  1.799 

    2.Association of 3-methylglutaconic aciduria type IV in patients with glycogen storage disease I

    Law, LK, Tang, NLS,     More...

    JOURNAL OF INHERITED METABOLIC DISEASE[0141-8955], Published 2007, Volume 30, Pages 40-40

    收錄情况: WOS

    WOS核心合集引用:  2023影響因子:  4.2  发表年影響因子:  1.668 

    3.Detection of fatty acid oxidation defects using simultaneous measurements of total fatty acid beta-oxidation flux and acylcarnitine profiling in fibroblasts cultured with (2)H31-palmitate by isotope ratio mass spectrometry and electrospray tandem mass spectrometry

    Law, LK, Tang, NLS,     More...

    JOURNAL OF INHERITED METABOLIC DISEASE[0141-8955], Published 2007, Volume 30, Pages 46-46

    收錄情况: WOS

    WOS核心合集引用:  2023影響因子:  4.2  发表年影響因子:  1.668 

    4.Total acylcarnitine level determined by in-vitro probe assay using (2)H31-palmitate can differentiate carnitine uptake defect from other fatty acid oxidation disorders

    Law, LK, Tang, NLS,     More...

    JOURNAL OF INHERITED METABOLIC DISEASE[0141-8955], Published 2007, Volume 30, Pages 47-47

    收錄情况: WOS

    WOS核心合集引用:  2023影響因子:  4.2  发表年影響因子:  1.668 

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