Liang C - Search Results

1

Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations.

Sue CM, Balasubramaniam S, Bratkovic D, Bonifant C, Christodoulou J, Coman D, Crawley K, Edema-Hildebrand F, Ellaway C, Ghaoui R, Kava M, Kearns LS, Lee J, Liang C, Mackey DA, Murray S, Needham M, Rius R, Russell J, Smith NJC, Thyagarajan D, Wools C. Sue CM, et al. Among authors: liang c. Intern Med J. 2022 Jan;52(1):110-120. doi: 10.1111/imj.15505. Epub 2021 Nov 19. Intern Med J. 2022. PMID: 34505344 Free PMC article.

2

Axonal hyperpolarization in inclusion-body myopathy, Paget disease of the bone, and frontotemporal dementia (IBMPFD).

Kumar KR, Liang C, Needham M, Burke D, Sue CM, Ng K. Kumar KR, et al. Among authors: liang c. Muscle Nerve. 2011 Aug;44(2):191-6. doi: 10.1002/mus.22020. Epub 2011 May 23. Muscle Nerve. 2011. PMID: 21607982

3

Necrotizing autoimmune myopathy.

Liang C, Needham M. Liang C, et al. Curr Opin Rheumatol. 2011 Nov;23(6):612-9. doi: 10.1097/BOR.0b013e32834b324b. Curr Opin Rheumatol. 2011. PMID: 21885975 Review.

4

POLG mutations in Australian patients with mitochondrial disease.

Woodbridge P, Liang C, Davis RL, Vandebona H, Sue CM. Woodbridge P, et al. Among authors: liang c. Intern Med J. 2013 Feb;43(2):150-6. doi: 10.1111/j.1445-5994.2012.02847.x. Intern Med J. 2013. PMID: 22647225

5

SPAST mutations in Australian patients with hereditary spastic paraplegia.

Vandebona H, Kerr NP, Liang C, Sue CM. Vandebona H, et al. Among authors: liang c. Intern Med J. 2012 Dec;42(12):1342-7. doi: 10.1111/j.1445-5994.2012.02941.x. Intern Med J. 2012. PMID: 23252998

6

Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegia.

Kumar KR, Blair NF, Vandebona H, Liang C, Ng K, Sharpe DM, Grünewald A, Gölnitz U, Saviouk V, Rolfs A, Klein C, Sue CM. Kumar KR, et al. Among authors: liang c. J Neurol. 2013 Oct;260(10):2516-22. doi: 10.1007/s00415-013-7008-x. Epub 2013 Jun 28. J Neurol. 2013. PMID: 23812641

7

Fibroblast growth factor 21 is a sensitive biomarker of mitochondrial disease.

Davis RL, Liang C, Edema-Hildebrand F, Riley C, Needham M, Sue CM. Davis RL, et al. Among authors: liang c. Neurology. 2013 Nov 19;81(21):1819-26. doi: 10.1212/01.wnl.0000436068.43384.ef. Epub 2013 Oct 18. Neurology. 2013. PMID: 24142477

8

The broadening spectrum of mitochondrial disease: shifts in the diagnostic paradigm.

Liang C, Ahmad K, Sue CM. Liang C, et al. Biochim Biophys Acta. 2014 Apr;1840(4):1360-7. doi: 10.1016/j.bbagen.2013.10.040. Epub 2013 Nov 13. Biochim Biophys Acta. 2014. PMID: 24239706 Free article. Review.

9

Systematic review of cardiac electrical disease in Kearns-Sayre syndrome and mitochondrial cytopathy.

Kabunga P, Lau AK, Phan K, Puranik R, Liang C, Davis RL, Sue CM, Sy RW. Kabunga P, et al. Among authors: liang c. Int J Cardiol. 2015 Feb 15;181:303-10. doi: 10.1016/j.ijcard.2014.12.038. Epub 2014 Dec 13. Int J Cardiol. 2015. PMID: 25540845 Review.

10

Expanding the phenotype of GMPPB mutations.

Cabrera-Serrano M, Ghaoui R, Ravenscroft G, Johnsen RD, Davis MR, Corbett A, Reddel S, Sue CM, Liang C, Waddell LB, Kaur S, Lek M, North KN, MacArthur DG, Lamont PJ, Clarke NF, Laing NG. Cabrera-Serrano M, et al. Among authors: liang c. Brain. 2015 Apr;138(Pt 4):836-44. doi: 10.1093/brain/awv013. Epub 2015 Feb 12. Brain. 2015. PMID: 25681410

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