Sui-Fan Tong
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Explore the profile of Sui-Fan Tong including associated specialties, affiliations and a list of published articles.
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Articles
31
Citations
159
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Recent Articles
1.
Mak C, Lam C, Tam S, Lai C, Chan L, Fan S, et al.
J Hum Genet
. 2020 Feb;
53(4):375.
PMID: 32041379
The correct name of the eighth author should be given as Sik-To Lai, not Jak-Yiu Lai.
2.
Cho S, Lam C, Tong S, Siu W
Clin Chim Acta
. 2013 Sep;
426:75-8.
PMID: 24055370
Background: Glycogen storage disease (GSD) is a group of inherited metabolic disorders due to enzymatic deficiency involved in glycogen breakdown. In various subtypes of GSD, GSD IXa is an X-linked...
3.
Wu J, Leung K, Tong S, Lam C
Rapid Commun Mass Spectrom
. 2011 Dec;
26(2):123-32.
PMID: 22173800
Organochlorines possess special isotopic patterns that obey the chlorine rule. In the case of triclosan (TCS), which contains three chlorine atoms, the isotopic patterns are composed of seven obvious peaks...
4.
Zha Y, Chen X, Lam C, Lee S, Tong S, Gao Z
Laryngoscope
. 2011 Jul;
121(8):1760-4.
PMID: 21792967
Objectives/hypothesis: Three Chinese patients with head and neck paragangliomas have been reported to carry the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene. In addition, in our hospital,...
5.
Siu W, Ma R, Lam C, Mak C, Yuen Y, Ivan Lo F, et al.
Chin Med J (Engl)
. 2011 Mar;
124(2):237-41.
PMID: 21362373
Background: Von Hippel-Lindau (VHL) syndrome is an autosomal dominant familial cancer syndrome predisposing the affected individuals to multiple tumours in various organs. The genetic basis of VHL in Southern Chinese...
6.
Lam C, Lau K, Tong S
Adv Clin Chem
. 2011 Feb;
52:1-18.
PMID: 21275337
The combination of single nucleotide polymorphisms (SNPs) database and high-density SNP array allows the use of SNPs as informative polymorphic markers for Mendelian diseases with complex traits efficiently. With the...
7.
Chau C, Kwok K, Ng D, Lam C, Tong S, Chan Y, et al.
Sleep Breath
. 2009 Aug;
14(2):161-5.
PMID: 19669818
Introduction: Leigh Syndrome is an uncommon cause of infantile apnea. Case Summary: We report a 5-month-old girl with sudden respiratory arrest followed by episodic hyper- and hypo-ventilation, encephalopathy, and persistent...
8.
WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b
Yuen Y, Cheng W, Tong S, Chan Y, Chan Y, Lam C
Mol Genet Metab
. 2009 Mar;
PMID: 19321372
This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can...
9.
Lam C, Kong A, Tsui T, Ozaki R, Chan H, Tong S, et al.
Clin Chim Acta
. 2008 Sep;
398(1-2):157-8.
PMID: 18760270
No abstract available.
10.
Mak C, Lam C, Tam S, Lai C, Chan L, Fan S, et al.
J Hum Genet
. 2007 Nov;
53(1):55-63.
PMID: 18034201
Wilson disease (WD), an autosomal recessive disorder of copper transport, is the most common inherited liver disorder in Hong Kong Chinese. This was the first local study to elucidate the...