Tomlinson B - Search Results

1

Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy.

Baum L, Haerian BS, Ng HK, Wong VC, Ng PW, Lui CH, Sin NC, Zhang C, Tomlinson B, Wong GW, Tan HJ, Raymond AA, Mohamed Z, Kwan P. Baum L, et al. Among authors: tomlinson b. Hum Genet. 2014 May;133(5):651-9. doi: 10.1007/s00439-013-1405-1. Epub 2013 Dec 13. Hum Genet. 2014. PMID: 24337656

2

Fatal accidental aconitine poisoning following ingestion of Chinese herbal medicine: a report of two cases.

Dickens P, Tai YT, But PP, Tomlinson B, Ng HK, Yan KW. Dickens P, et al. Among authors: tomlinson b. Forensic Sci Int. 1994 Jun 28;67(1):55-8. doi: 10.1016/0379-0738(94)90412-x. Forensic Sci Int. 1994. PMID: 8082861

3

Compound heterozygosity of Leu252Val and Leu252Arg causing lipoprotein lipase deficiency in a chinese patient with hypertriglyceridemia.

Chan L, Mak Y, Tomlinson B, Baum L, Wu X, Masarei J, Pang C. Chan L, et al. Among authors: tomlinson b. Eur J Clin Invest. 2000 Jan;30(1):33-40. doi: 10.1046/j.1365-2362.2000.00587.x. Eur J Clin Invest. 2000. PMID: 10619999

4

Genotype-phenotype studies of six novel LPL mutations in Chinese patients with hypertriglyceridemia.

Chan LY, Lam CW, Mak YT, Tomlinson B, Tsang MW, Baum L, Masarei JR, Pang CP. Chan LY, et al. Among authors: tomlinson b. Hum Mutat. 2002 Sep;20(3):232-3. doi: 10.1002/humu.9054. Hum Mutat. 2002. PMID: 12204001

5

Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes.

Yang T, Pang CP, Tsang MW, Lam CW, Poon PM, Chan LY, Wu XQ, Tomlinson B, Baum L. Yang T, et al. Among authors: tomlinson b. Hum Mutat. 2003 Apr;21(4):453. doi: 10.1002/humu.9134. Hum Mutat. 2003. PMID: 12655575

6

APOA5-1131T>C polymorphism is associated with triglyceride levels in Chinese men.

Baum L, Tomlinson B, Thomas GN. Baum L, et al. Among authors: tomlinson b. Clin Genet. 2003 May;63(5):377-9. doi: 10.1034/j.1399-0004.2003.00063.x. Clin Genet. 2003. PMID: 12752569

7

Methylenetetrahydrofolate reductase gene A222V polymorphism and risk of ischemic stroke.

Baum L, Wong KS, Ng HK, Tomlinson B, Rainer TH, Chan DK, Thomas GN, Chen X, Poon P, Cheung WS, Woo KS. Baum L, et al. Among authors: tomlinson b. Clin Chem Lab Med. 2004;42(12):1370-6. doi: 10.1515/CCLM.2004.256. Clin Chem Lab Med. 2004. PMID: 15576298

8

Effect of hepatic lipase -514C->T polymorphism and its interactions with apolipoprotein C3 -482C->T and apolipoprotein E exon 4 polymorphisms on the risk of nephropathy in chinese type 2 diabetic patients.

Baum L, Ng MC, So WY, Lam VK, Wang Y, Poon E, Tomlinson B, Cheng S, Lindpaintner K, Chan JC. Baum L, et al. Among authors: tomlinson b. Diabetes Care. 2005 Jul;28(7):1704-9. doi: 10.2337/diacare.28.7.1704. Diabetes Care. 2005. PMID: 15983323

9

Paraoxonase 1 gene Q192R polymorphism affects stroke and myocardial infarction risk.

Baum L, Ng HK, Woo KS, Tomlinson B, Rainer TH, Chen X, Cheung WS, Chan DK, Thomas GN, Tong CS, Wong KS. Baum L, et al. Among authors: tomlinson b. Clin Biochem. 2006 Mar;39(3):191-5. doi: 10.1016/j.clinbiochem.2006.01.010. Epub 2006 Feb 9. Clin Biochem. 2006. PMID: 16472799

10

Associations of apolipoprotein E exon 4 and lipoprotein lipase S447X polymorphisms with acute ischemic stroke and myocardial infarction.

Baum L, Ng HK, Wong KS, Tomlinson B, Rainer TH, Chen X, Cheung WS, Tang J, Tam WW, Goggins W, Tong CS, Chan DK, Thomas GN, Chook P, Woo KS. Baum L, et al. Among authors: tomlinson b. Clin Chem Lab Med. 2006;44(3):274-81. doi: 10.1515/CCLM.2006.047. Clin Chem Lab Med. 2006. PMID: 16519597 Free article.

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