Sue CM - Search Results

1

Dystonia Responsive to Dopamine: POLG Mutations Should Be Considered If Sensory Neuropathy Is Present.

Qiu J, Kumar KR, Watson E, Ahmad K, Sue CM, Hayes MW. Qiu J, et al. Among authors: sue cm. J Mov Disord. 2021 May;14(2):157-160. doi: 10.14802/jmd.20159. Epub 2021 May 26. J Mov Disord. 2021. PMID: 34062649 Free PMC article.

2

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: sue cm. Muscle Nerve. 2010 Mar;41(3):412-5. doi: 10.1002/mus.21610. Muscle Nerve. 2010. PMID: 20120005

3

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: sue cm. 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

4

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

5

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: sue cm. 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

6

POLG mutations in Australian patients with mitochondrial disease.

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

7

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: sue cm. Mov Disord. 2012 Jul;27(8):1034-40. doi: 10.1002/mds.25033. Epub 2012 Jun 26. Mov Disord. 2012. PMID: 22736418

8

Frequency of the D620N mutation in VPS35 in Parkinson disease.

Kumar KR, Weissbach A, Heldmann M, Kasten M, Tunc S, Sue CM, Svetel M, Kostić VS, Segura-Aguilar J, Ramirez A, Simon DK, Vieregge P, Münte TF, Hagenah J, Klein C, Lohmann K. Kumar KR, et al. Among authors: sue cm. Arch Neurol. 2012 Oct;69(10):1360-4. doi: 10.1001/archneurol.2011.3367. Arch Neurol. 2012. PMID: 22801713

9

Phenotypic variability of parkin mutations in single kindred.

Koentjoro B, Park JS, Ha AD, Sue CM. Koentjoro B, et al. Among authors: sue cm. Mov Disord. 2012 Sep 1;27(10):1299-303. doi: 10.1002/mds.25041. Epub 2012 Jul 17. Mov Disord. 2012. PMID: 22807239

10

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

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