Chung BH - Search Results

1

Mutation of gene in spinal muscular atrophy respiratory distress type I.

Wong VC, Chung BH, Li S, Goh W, Lee SL. Wong VC, et al. Among authors: chung bh. Pediatr Neurol. 2006 Jun;34(6):474-7. doi: 10.1016/j.pediatrneurol.2005.10.022. Pediatr Neurol. 2006. PMID: 16765827

2

Survey of public awareness, attitudes, and understanding toward epilepsy in Hong Kong.

Wong V, Chung BH. Wong V, et al. Among authors: chung bh. Epilepsia. 2003 Feb;44(2):268-9; author reply 269-70. doi: 10.1046/j.1528-1157.2003.510023.x. Epilepsia. 2003. PMID: 12558589 Free article. No abstract available.

3

Subacute sclerosing panencephalitis in children: prevalence in South China.

Ip P, Chung BH, Wong VC, Chan KY. Ip P, et al. Among authors: chung bh. Pediatr Neurol. 2004 Jul;31(1):46-51. doi: 10.1016/j.pediatrneurol.2003.11.010. Pediatr Neurol. 2004. PMID: 15246492

4

The evaluation of Wallerian degeneration in chronic paediatric middle cerebral artery infarction using diffusion tensor MR imaging.

Khong PL, Zhou LJ, Ooi GC, Chung BH, Cheung RT, Wong VC. Khong PL, et al. Among authors: chung bh. Cerebrovasc Dis. 2004;18(3):240-7. doi: 10.1159/000079961. Epub 2004 Jul 23. Cerebrovasc Dis. 2004. PMID: 15273442

5

Acute fulminant subacute sclerosing panencephalitis with absent measles and PCR studies in cerebrospinal fluid.

Chung BH, Ip PP, Wong VC, Lo JY, Harding B. Chung BH, et al. Pediatr Neurol. 2004 Sep;31(3):222-4. doi: 10.1016/j.pediatrneurol.2004.03.016. Pediatr Neurol. 2004. PMID: 15351025

6

Spinal muscular atrophy: survival pattern and functional status.

Chung BH, Wong VC, Ip P. Chung BH, et al. Pediatrics. 2004 Nov;114(5):e548-53. doi: 10.1542/peds.2004-0668. Epub 2004 Oct 18. Pediatrics. 2004. PMID: 15492357

7

Neurologic complications in children hospitalized with influenza: comparison between USA and Hong Kong.

Chung BH, Tsang AM, Wong VC. Chung BH, et al. J Pediatr. 2007 Nov;151(5):e17-8; author reply e18-9. doi: 10.1016/j.jpeds.2007.07.048. J Pediatr. 2007. PMID: 17961673 No abstract available.

8

Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: report and a review of literature.

Liu AP, Tang WF, Lau ET, Chan KY, Kan AS, Wong KY, Tso WW, Jalal K, Lee SL, Chau CS, Chung BH. Liu AP, et al. Among authors: chung bh. Am J Med Genet A. 2013 Jun;161A(6):1309-18. doi: 10.1002/ajmg.a.35909. Epub 2013 Apr 30. Am J Med Genet A. 2013. PMID: 23633107 Review.

9

The clinical impact of chromosomal microarray on paediatric care in Hong Kong.

Tao VQ, Chan KY, Chu YW, Mok GT, Tan TY, Yang W, Lee SL, Tang WF, Tso WW, Lau ET, Kan AS, Tang MH, Lau YL, Chung BH. Tao VQ, et al. Among authors: chung bh. PLoS One. 2014 Oct 15;9(10):e109629. doi: 10.1371/journal.pone.0109629. eCollection 2014. PLoS One. 2014. PMID: 25333781 Free PMC article.

10

Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion.

Chiu ATG, Pei SLC, Mak CCY, Leung GKC, Yu MHC, Lee SL, Vreeburg M, Pfundt R, van der Burgt I, Kleefstra T, Frederic TM, Nambot S, Faivre L, Bruel AL, Rossi M, Isidor B, Küry S, Cogne B, Besnard T, Willems M, Reijnders MRF, Chung BHY. Chiu ATG, et al. Clin Genet. 2018 Apr;93(4):880-890. doi: 10.1111/cge.13196. Epub 2018 Feb 13. Clin Genet. 2018. PMID: 29240241

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