Leung GK - Search Results

1

A novel patient with an attenuated Costello syndrome phenotype due to an HRAS mutation affecting codon 146-Literature review and update.

Chiu AT, Leung GK, Chu YW, Gripp KW, Chung BH. Chiu AT, et al. Among authors: leung gk. Am J Med Genet A. 2017 Apr;173(4):1109-1114. doi: 10.1002/ajmg.a.38118. Am J Med Genet A. 2017. PMID: 28328122

2

Mosaic KRAS mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension.

McDonell LM, Leung GK, Daoud H, Ip J, Chim S, Luk HM, Lan L; Care4Rare Canada Consortium; Boycott KM, Chung BH. McDonell LM, et al. Among authors: leung gk. Am J Med Genet A. 2018 Nov;176(11):2523-2527. doi: 10.1002/ajmg.a.40349. Epub 2018 Oct 5. Am J Med Genet A. 2018. PMID: 30289595 No abstract available.

3

Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autism.

Yeung KS, Tso WWY, Ip JJK, Mak CCY, Leung GKC, Tsang MHY, Ying D, Pei SLC, Lee SL, Yang W, Chung BH. Yeung KS, et al. Mol Autism. 2017 Dec 20;8:66. doi: 10.1186/s13229-017-0182-4. eCollection 2017. Mol Autism. 2017. PMID: 29296277 Free PMC article.

4

Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10.

Mak ASL, Chiu ATG, Leung GKC, Mak CCY, Chu YWY, Mok GTK, Tang WF, Chan KYK, Tang MHY, Lau Yim ET, So KW, Tao VQ, Fung CW, Wong VCN, Uddin M, Lee SL, Marshall CR, Scherer SW, Kan ASY, Chung BHY. Mak ASL, et al. Mol Autism. 2017 Jun 26;8:31. doi: 10.1186/s13229-017-0136-x. eCollection 2017. Mol Autism. 2017. PMID: 28670437 Free PMC article.

5

Exome sequencing identifies molecular diagnosis in children with drug-resistant epilepsy.

Tsang MH, Leung GK, Ho AC, Yeung KS, Mak CC, Pei SL, Yu MH, Kan AS, Chan KY, Kwong KL, Lee SL, Yung AW, Fung CW, Chung BH. Tsang MH, et al. Among authors: leung gk. Epilepsia Open. 2018 Dec 6;4(1):63-72. doi: 10.1002/epi4.12282. eCollection 2019 Mar. Epilepsia Open. 2018. PMID: 30868116 Free PMC article.

6

Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong.

Chung CCY, Chan KYK, Hui PW, Au PKC, Tam WK, Li SKM, Leung GKC, Fung JLF, Chan MCY, Luk HM, Mak ASL, Leung KY, Tang MHY, Chung BHY, Kan ASY. Chung CCY, et al. BMC Pregnancy Childbirth. 2020 Feb 14;20(1):109. doi: 10.1186/s12884-020-2772-y. BMC Pregnancy Childbirth. 2020. PMID: 32059709 Free PMC article.

7

Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay.

Yeung KS, Ho MSP, Lee SL, Kan ASY, Chan KYK, Tang MHY, Mak CCY, Leung GKC, So PL, Pfundt R, Marshall CR, Scherer SW, Choufani S, Weksberg R, Hon-Yin Chung B. Yeung KS, et al. J Med Genet. 2018 Dec;55(12):847-852. doi: 10.1136/jmedgenet-2018-105328. Epub 2018 Jul 14. J Med Genet. 2018. PMID: 30007940

8

Sirtuin 5 (SIRT5) Suppresses Tumor Growth by Regulating Mitochondrial Metabolism and Synaptic Remodeling in Gliomas.

Tang W, Chen B, Leung GK, Kiang KM. Tang W, et al. Among authors: leung gk. Int J Mol Sci. 2024 Aug 22;25(16):9125. doi: 10.3390/ijms25169125. Int J Mol Sci. 2024. PMID: 39201811 Free PMC article.

9

Acute calcitriol treatment mitigates vitamin D deficiency-associated mortality after intracerebral haemorrhage.

Chan AA, Lam TL, Liu J, Ng AC, Zhang C, Kiang KM, Leung GK. Chan AA, et al. Among authors: leung gk. Neurosci Lett. 2024 Aug 24;838:137922. doi: 10.1016/j.neulet.2024.137922. Epub 2024 Aug 8. Neurosci Lett. 2024. PMID: 39127125

10

Interventions in the workplace to reduce risk factors for noncommunicable diseases: an umbrella review of systematic reviews of effectiveness.

Turon H, Bezzina A, Lamont H, Barnes C, Lum M, Hodder RK, Leung GKW, Peeters A, Wolfenden L, Yoong S. Turon H, et al. Among authors: leung gkw. J Occup Health. 2024 Jan 4;66(1):uiae044. doi: 10.1093/joccuh/uiae044. J Occup Health. 2024. PMID: 39096275 Free article. Review.

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