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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.
Health-related quality of life of children with epilepsy in Hong Kong: how does it compare with that of youth with epilepsy in Canada?
Yam WK, Ronen GM, Cherk SW, Rosenbaum P, Chan KY, Streiner DL, Cheng SW, Fung CW, Ho JC, Kwong KL, Ma LC, Ma DK, Tsui KW, Wong V, Wong TY.
Yam WK, et al.
Epilepsy Behav. 2008 Apr;12(3):419-26. doi: 10.1016/j.yebeh.2007.11.007. Epub 2007 Dec 26.
Epilepsy Behav. 2008.
PMID: 18158271
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Factor structure and construct validity of the Chinese Health-Related Quality of Life Measure for Youth with Epilepsy.
Yam WK, Ma DK, Cherk SW; Working Group for Multi-Centre Study on Quality of Life Measures for Youth with Epilepsy.
Yam WK, et al.
Epilepsy Behav. 2006 Dec;9(4):606-18. doi: 10.1016/j.yebeh.2006.08.016. Epub 2006 Sep 29.
Epilepsy Behav. 2006.
PMID: 17011241
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Health-related quality of life in Chinese boys with Duchenne muscular dystrophy and their families.
Liang R, Chan SHS, Ho FKW, Tang OC, Cherk SWW, Ip P, Lau EYY.
Liang R, et al. Among authors: cherk sww.
J Child Health Care. 2019 Sep;23(3):495-506. doi: 10.1177/1367493519857423. Epub 2019 Jun 20.
J Child Health Care. 2019.
PMID: 31220930
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Anti-N-methyl-d-aspartate receptor encephalitis in children: Incidence and experience in Hong Kong.
Ho AC, Chan SH, Chan E, Wong SS, Fung ST, Cherk SW, Fung EL, Ma KH, Tsui KW, Yau EK, Wong VC.
Ho AC, et al.
Brain Dev. 2018 Jun;40(6):473-479. doi: 10.1016/j.braindev.2018.02.005. Epub 2018 Mar 26.
Brain Dev. 2018.
PMID: 29599011
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Hyperekplexia: a Chinese adolescent with 2 novel mutations of the GLRA1 gene.
Chan KK, Cherk SW, Lee HH, Poon WT, Chan AY.
Chan KK, et al.
J Child Neurol. 2014 Jan;29(1):111-3. doi: 10.1177/0883073812465338. Epub 2012 Nov 8.
J Child Neurol. 2014.
PMID: 23143726
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A novel ALDH5A1 mutation in a patient with succinic semialdehyde dehydrogenase deficiency.
Kwok JS, Yuen CL, Law LK, Tang NL, Cherk SW, Yuen YP.
Kwok JS, et al.
Pathology. 2012 Apr;44(3):280-2. doi: 10.1097/PAT.0b013e32835140c2.
Pathology. 2012.
PMID: 22437753
No abstract available.
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Review of children with severe trauma or thermal injury requiring intensive care in a Hong Kong hospital: retrospective study.
Ng DK, Cherk SW, Yu WL, Lau MY, Ho JC, Chau CK.
Ng DK, et al.
Hong Kong Med J. 2002 Apr;8(2):82-6.
Hong Kong Med J. 2002.
PMID: 11937661
Free article.
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