Ng K - Search Results

1

The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome.

Ha AD, Parratt KL, Rendtorff ND, Lodahl M, Ng K, Rowe DB, Sue CM, Hayes MW, Tranebjaerg L, Fung VS. Ha AD, et al. Among authors: ng k. Mov Disord. 2012 Jul;27(8):1034-40. doi: 10.1002/mds.25033. Epub 2012 Jun 26. Mov Disord. 2012. PMID: 22736418

2

Facial nerve palsy after intracisternal papaverine application during aneurysm surgery--case report.

Lang EW, Neugebauer M, Ng K, Fung V, Clouston P, Dorsch NW. Lang EW, et al. Among authors: ng k. Neurol Med Chir (Tokyo). 2002 Dec;42(12):565-7. doi: 10.2176/nmc.42.565. Neurol Med Chir (Tokyo). 2002. PMID: 12513030 Free article.

3

A novel CLCN1 mutation (G1652A) causing a mild phenotype of thomsen disease.

Kumar KR, Ng K, Vandebona H, Davis MR, Sue CM. Kumar KR, et al. Among authors: ng k. Muscle Nerve. 2010 Mar;41(3):412-5. doi: 10.1002/mus.21610. Muscle Nerve. 2010. PMID: 20120005

4

Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings.

Kumar KR, Needham M, Mina K, Davis M, Brewer J, Staples C, Ng K, Sue CM, Mastaglia FL. Kumar KR, et al. Among authors: ng k. Neuromuscul Disord. 2010 May;20(5):330-4. doi: 10.1016/j.nmd.2010.03.002. Epub 2010 Mar 23. Neuromuscul Disord. 2010. PMID: 20335036

5

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: ng k. Muscle Nerve. 2011 Aug;44(2):191-6. doi: 10.1002/mus.22020. Epub 2011 May 23. Muscle Nerve. 2011. PMID: 21607982

6

Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation--a neurophysiological study using excitability techniques.

Kumar KR, Sue CM, Burke D, Ng K. Kumar KR, et al. Among authors: ng k. Clin Neurophysiol. 2012 Jul;123(7):1454-9. doi: 10.1016/j.clinph.2011.11.080. Epub 2011 Dec 21. Clin Neurophysiol. 2012. PMID: 22192498

7

Axonal excitability during ischemia in MELAS.

Ng K, Kumar KR, Sue C, Burke D. Ng K, et al. Muscle Nerve. 2013 May;47(5):762-5. doi: 10.1002/mus.23733. Epub 2013 Mar 29. Muscle Nerve. 2013. PMID: 23553640

8

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: ng k. J Neurol. 2013 Oct;260(10):2516-22. doi: 10.1007/s00415-013-7008-x. Epub 2013 Jun 28. J Neurol. 2013. PMID: 23812641

9

High Degree of Genetic Heterogeneity for Hereditary Cerebellar Ataxias in Australia.

Kang C, Liang C, Ahmad KE, Gu Y, Siow SF, Colebatch JG, Whyte S, Ng K, Cremer PD, Corbett AJ, Davis RL, Roscioli T, Cowley MJ, Park JS, Sue CM, Kumar KR. Kang C, et al. Among authors: ng k. Cerebellum. 2019 Feb;18(1):137-146. doi: 10.1007/s12311-018-0969-7. Cerebellum. 2019. PMID: 30078120

10

Motor Evoked Potentials in Hereditary Spastic Paraplegia-A Systematic Review.

Siow SF, Cameron Smail R, Ng K, Kumar KR, Sue CM. Siow SF, et al. Among authors: ng k. Front Neurol. 2019 Sep 18;10:967. doi: 10.3389/fneur.2019.00967. eCollection 2019. Front Neurol. 2019. PMID: 31620065 Free PMC article.

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