排序方式:
1.3-methylglutaconic aciduria in a Chinese patient with glycogen storage disease Ib
Law, LK, Tang, NLS,
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Law, LK, Tang, NLS, Hui, J, Lam, CWK, Fok, TF
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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,
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Law, LK, Tang, NLS, Chien, YH, Hui, J, But, BWM, Ma, KC, Hwu, WL, Shek, CC, Fok, TF, Lam, CWK
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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: 0
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,
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Law, LK, Tang, NLS, Hui, J, Pang, EWH, Ho, CS, Ruiter, J, Fok, TF, Wanders, RJA, Lam, CWK
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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: 0
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,
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Law, LK, Tang, NLS, Hui, J, Chien, YH, Hwu, WL, Pang, EWH, Fung, SLM, Ho, CS, Ruiter, J, Fok, TF, Wanders, RJA, Lam, CWK
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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: 0
2023影響因子:
4.2
发表年影響因子:
1.668