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Prevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy: A Territory Wide Collaborative Study in Hong Kong.
Child Neurol Open. 2015 May 26;2(2):2329048X15585345. doi: 10.1177/2329048X15585345. eCollection 2015 Apr-Jun.
Child Neurol Open. 2015.
PMID: 28503591
Free PMC article.
Reduction in Myoclonus and Ataxia Following the Use of Perampanel in Patient With Sialidosis Type 1.
So ECT, Mak CM, Ng GSF, Tsui KW, Ma KH, Yeung WL.
So ECT, et al. Among authors: ng gsf.
Pediatr Neurol. 2020 Aug;109:91-93. doi: 10.1016/j.pediatrneurol.2020.03.004. Epub 2020 Apr 13.
Pediatr Neurol. 2020.
PMID: 32299749
No abstract available.
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Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.
Siu WK, Lam CW, Mak CM, Lau ET, Tang MH, Tang WF, Poon-Mak RS, Lee CC, Hung SF, Leung PW, Kwong KL, Yau EK, Ng GS, Fong NC, Chan KY.
Siu WK, et al.
Clin Transl Med. 2016 Dec;5(1):18. doi: 10.1186/s40169-016-0098-1. Epub 2016 May 16.
Clin Transl Med. 2016.
PMID: 27271878
Free PMC article.
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Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.
Law CY, Chang ST, Cho SY, Yau EK, Ng GS, Fong NC, Lam CW.
Law CY, et al.
Clin Chim Acta. 2015 Dec 7;451(Pt B):292-6. doi: 10.1016/j.cca.2015.10.011. Epub 2015 Oct 17.
Clin Chim Acta. 2015.
PMID: 26485252
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DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.
Lam CW, Li CK, Lai CK, Tong SF, Chan KY, Ng GS, Yuen YP, Cheng AW, Chan YW.
Lam CW, et al.
Mol Genet Metab. 2002 Jan;75(1):91-5. doi: 10.1006/mgme.2001.3267.
Mol Genet Metab. 2002.
PMID: 11825068
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