Keng WT - Search Results

1

Clinical, biochemical and genetic profiles of patients with mucopolysaccharidosis type IVA (Morquio A syndrome) in Malaysia: the first national natural history cohort study.

Leong HY, Abdul Azize NA, Chew HB, Keng WT, Thong MK, Mohd Khalid MKN, Hung LC, Mohamed Zainudin N, Ramlee A, Md Haniffa MA, Yakob Y, Ngu LH. Leong HY, et al. Among authors: keng wt. Orphanet J Rare Dis. 2019 Jun 14;14(1):143. doi: 10.1186/s13023-019-1105-6. Orphanet J Rare Dis. 2019. PMID: 31200731 Free PMC article.

2

Fructose-1,6-bisphosphatase deficiency as a cause of recurrent hypoglycemia and metabolic acidosis: Clinical and molecular findings in Malaysian patients.

Moey LH, Abdul Azize NA, Yakob Y, Leong HY, Keng WT, Chen BC, Ngu LH. Moey LH, et al. Among authors: keng wt. Pediatr Neonatol. 2018 Aug;59(4):397-403. doi: 10.1016/j.pedneo.2017.11.006. Epub 2017 Nov 13. Pediatr Neonatol. 2018. PMID: 29203193 Free article.

3

Neonatal intrahepatic cholestasis associated with citrin deficiency (NICCD): a case series of 11 Malaysian patients.

Chew HB, Ngu LH, Zabedah MY, Keng WT, Balasubramaniam S, Hanifah MJ, Kobayashi K. Chew HB, et al. Among authors: keng wt. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S489-95. doi: 10.1007/s10545-010-9248-6. Epub 2010 Dec 16. J Inherit Metab Dis. 2010. PMID: 21161389

4

Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation (ROHHAD): a case with additional features and review of the literature.

Chew HB, Ngu LH, Keng WT. Chew HB, et al. Among authors: keng wt. BMJ Case Rep. 2011 Mar 1;2011:bcr0220102706. doi: 10.1136/bcr.02.2010.2706. BMJ Case Rep. 2011. PMID: 22715259 Free PMC article. Review.

5

Treatment of Lesch-Nyhan disease with S-adenosylmethionine: experience with five young Malaysians, including a girl.

Chen BC, Balasubramaniam S, McGown IN, O'Neill JP, Chng GS, Keng WT, Ngu LH, Duley JA. Chen BC, et al. Among authors: keng wt. Brain Dev. 2014 Aug;36(7):593-600. doi: 10.1016/j.braindev.2013.08.013. Epub 2013 Sep 18. Brain Dev. 2014. PMID: 24055166

6

Mowat-Wilson syndrome: the first two Malaysian cases.

Balasubramaniam S, Keng WT, Ngu LH, Michel LG, Irina G. Balasubramaniam S, et al. Among authors: keng wt. Singapore Med J. 2010 Mar;51(3):e54-7. Singapore Med J. 2010. PMID: 20428734 Free article.

7

Pilot study of newborn screening of inborn error of metabolism using tandem mass spectrometry in Malaysia: outcome and challenges.

Yunus ZM, Rahman SA, Choy YS, Keng WT, Ngu LH. Yunus ZM, et al. Among authors: keng wt. J Pediatr Endocrinol Metab. 2016 Sep 1;29(9):1031-9. doi: 10.1515/jpem-2016-0028. J Pediatr Endocrinol Metab. 2016. PMID: 27544719

8

Combination of Multiple Ligation-Dependent Probe Amplification and Illumina MiSeq Amplicon Sequencing for TSC1/TSC2 Gene Analyses in Patients with Tuberous Sclerosis Complex.

Ismail NF, Rani AQ, Nik Abdul Malik NM, Boon Hock C, Mohd Azlan SN, Abdul Razak S, Keng WT, Ngu LH, Silawati AR, Yahya NA, Mohd Yusoff N, Sasongko TH, Zabidi-Hussin ZA. Ismail NF, et al. Among authors: keng wt. J Mol Diagn. 2017 Mar;19(2):265-276. doi: 10.1016/j.jmoldx.2016.10.009. Epub 2017 Jan 11. J Mol Diagn. 2017. PMID: 28087349 Free article.

9

Two novel gross deletions of TSC2 in Malaysian patients with tuberous sclerosis complex and TSC2/PKD1 contiguous deletion syndrome.

Ismail NF, Nik Abdul Malik NM, Mohseni J, Rani AM, Hayati F, Salmi AR, Narazah MY, Zabidi-Hussin ZA, Silawati AR, Keng WT, Ngu LH, Sasongko TH. Ismail NF, et al. Among authors: keng wt. Jpn J Clin Oncol. 2014 May;44(5):506-11. doi: 10.1093/jjco/hyu024. Epub 2014 Mar 30. Jpn J Clin Oncol. 2014. PMID: 24683199

10

Mutational analyses on X-linked adrenoleukodystrophy reveal a novel cryptic splicing and three missense mutations in the ABCD1 gene.

Hung KL, Wang JS, Keng WT, Chen HJ, Liang JS, Ngu LH, Lu JF. Hung KL, et al. Among authors: keng wt. Pediatr Neurol. 2013 Sep;49(3):185-90. doi: 10.1016/j.pediatrneurol.2013.04.021. Epub 2013 Jul 5. Pediatr Neurol. 2013. PMID: 23835273

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