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Year | Number of Results |
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Page 1
Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscape.
Orphanet J Rare Dis. 2023 Mar 2;18(1):43. doi: 10.1186/s13023-023-02632-6.
Orphanet J Rare Dis. 2023.
PMID: 36859275
Free PMC article.
Guillain-Barré syndrome in children - High occurrence of Miller Fisher syndrome in East Asian region.
Chiu ATG, Chan RWK, Yau MLY, Yuen ACL, Lam AKF, Lau SWY, Lau AMC, Fung STH, Ma KH, Lau CWL, Yau MM, Ko CH, Tsui KW, Ma CK, Tai SM, Yau EKC, Fung E, Wu SP, Kwong KL, Chan SHS.
Chiu ATG, et al. Among authors: wu sp.
Brain Dev. 2022 Nov;44(10):715-724. doi: 10.1016/j.braindev.2022.07.003. Epub 2022 Jul 26.
Brain Dev. 2022.
PMID: 35906115
Free article.
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Correlation of urodynamic studies and somatosensory evoked potential and their prognostic value in children with closed spinal dysraphism.
Hung JW, Chow JS, Kuok MC, Lam AK, Lee JL, Yam FS, Chung KL, Wu SP, Cheung FC, Chan WK, Leung MW.
Hung JW, et al. Among authors: wu sp.
J Pediatr Urol. 2023 Apr;19(2):193.e1-193.e8. doi: 10.1016/j.jpurol.2022.12.004. Epub 2022 Dec 9.
J Pediatr Urol. 2023.
PMID: 36566130
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Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population.
Tsang MHY, Kwong AKY, Chan KLS, Fung JLF, Yu MHC, Mak CCY, Yeung KS, Rodenburg RJT, Smeitink JAM, Chan R, Tsoi T, Hui J, Wong SSN, Tai SM, Chan VCM, Ma CK, Fung STH, Wu SP, Chak WK, Chung BHY, Fung CW.
Tsang MHY, et al. Among authors: wu sp.
Hum Genomics. 2020 Sep 10;14(1):28. doi: 10.1186/s40246-020-00278-0.
Hum Genomics. 2020.
PMID: 32907636
Free PMC article.
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Spinal Muscular Atrophy With Respiratory Distress Type 1-A Child With Atypical Presentation.
Chiu ATG, Chan SHS, Wu SP, Ting SH, Chung BHY, Chan AOK, Wong VCN.
Chiu ATG, et al. Among authors: wu sp.
Child Neurol Open. 2018 Apr 19;5:2329048X18769811. doi: 10.1177/2329048X18769811. eCollection 2018.
Child Neurol Open. 2018.
PMID: 29761130
Free PMC article.
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Prevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy: A Territory Wide Collaborative Study in Hong Kong.
Chan SHS, Lo IFM, Cherk SWW, Cheng WW, Fung ELW, Yeung WL, Ngan M, Lee WC, Kwong L, Wong SN, Ma CK, Tai SM, Ng GSF, Wu SP, Wong VCN.
Chan SHS, et al. Among authors: wu sp.
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.
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Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease.
Yeung WL, Lam CW, Hui J, Tong SF, Wu SP.
Yeung WL, et al. Among authors: wu sp.
Brain Dev. 2006 Jul;28(6):389-91. doi: 10.1016/j.braindev.2005.10.012. Epub 2006 Jan 10.
Brain Dev. 2006.
PMID: 16376043
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