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Items: 21

1.

Establishment and 12-month progress of the New Zealand Motor Neurone Disease Registry.

Walker KL, Rodrigues MJ, Watson B, Reilly C, Scotter EL, Brunton H, Turnbull J, Roxburgh RH.

J Clin Neurosci. 2019 Feb;60:7-11. doi: 10.1016/j.jocn.2018.11.034. Epub 2018 Nov 22. Review.

PMID:
30473407
2.

Impacts for Children Living with Genetic Muscle Disorders and their Parents - Findings from a Population-Based Study.

Jones KM, O'Grady G, Rodrigues MJ, Ranta A, Roxburgh RH, Love DR, Theadom A; MD-PREV study group.

J Neuromuscul Dis. 2018;5(3):341-352. doi: 10.3233/JND-170287.

PMID:
30040738
3.

Peripheral nerves are pathologically small in cerebellar ataxia neuropathy vestibular areflexia syndrome: a controlled ultrasound study.

Pelosi L, Mulroy E, Leadbetter R, Kilfoyle D, Chancellor AM, Mossman S, Wing L, Wu TY, Roxburgh RH.

Eur J Neurol. 2018 Apr;25(4):659-665. doi: 10.1111/ene.13563. Epub 2018 Feb 26.

PMID:
29316033
4.

Neuronopathy and neuropathy in autosomal dominant spino-cerebellar ataxia (SCA): A preliminary peripheral nerve ultrasound study.

Pelosi L, Mulroy E, Rodrigues MJ, Roxburgh RH.

Clin Neurophysiol. 2017 Dec;128(12):2436-2437. doi: 10.1016/j.clinph.2017.09.114. Epub 2017 Oct 12. No abstract available.

PMID:
29096217
5.

The New Zealand Neuromuscular Disease Patient Registry; Five Years and a Thousand Patients.

Rodrigues MJ, O'Grady GL, Hammond-Tooke G, Kidd A, Love DO, Baker RK, Roxburgh RH.

J Neuromuscul Dis. 2017;4(3):183-188. doi: 10.3233/JND-170240.

6.

Corneal nerve microstructure in Parkinson's disease.

Misra SL, Kersten HM, Roxburgh RH, Danesh-Meyer HV, McGhee CN.

J Clin Neurosci. 2017 May;39:53-58. doi: 10.1016/j.jocn.2017.02.033. Epub 2017 Mar 3.

PMID:
28268149
7.

Ophthalmic findings in myotonic dystrophy type 2: a case series.

Kersten HM, Danesh-Meyer HV, Roxburgh RH.

J Neurol. 2016 Dec;263(12):2552-2554. Epub 2016 Nov 2. No abstract available.

PMID:
27807619
8.

Globus pallidus degeneration and clinicopathological features of Huntington disease.

Singh-Bains MK, Tippett LJ, Hogg VM, Synek BJ, Roxburgh RH, Waldvogel HJ, Faull RL.

Ann Neurol. 2016 Aug;80(2):185-201. doi: 10.1002/ana.24694. Epub 2016 Jun 24.

PMID:
27255697
9.

Optical coherence tomography findings in a patient with type 1 sialidosis.

Kersten HM, Roxburgh RH, Danesh-Meyer HV, Hutchinson DO.

J Clin Neurosci. 2016 Sep;31:199-201. doi: 10.1016/j.jocn.2016.02.015. Epub 2016 Apr 1.

PMID:
27052257
10.

Optical coherence tomography findings in Huntington's disease: a potential biomarker of disease progression.

Kersten HM, Danesh-Meyer HV, Kilfoyle DH, Roxburgh RH.

J Neurol. 2015 Nov;262(11):2457-65. doi: 10.1007/s00415-015-7869-2. Epub 2015 Aug 2.

PMID:
26233693
11.

Congestive myeloradiculopathy in a patient with Cowden syndrome.

Wu TY, Willoughby E, Hutchinson DO, Brew S, McGuinness B, Lopes R, Love DR, Roxburgh RH.

J Clin Neurosci. 2015 Feb;22(2):431-3. doi: 10.1016/j.jocn.2014.07.023. Epub 2014 Oct 7.

PMID:
25304432
12.

Autonomic dysfunction is a major feature of cerebellar ataxia, neuropathy, vestibular areflexia 'CANVAS' syndrome.

Wu TY, Taylor JM, Kilfoyle DH, Smith AD, McGuinness BJ, Simpson MP, Walker EB, Bergin PS, Cleland JC, Hutchinson DO, Anderson NE, Snow BJ, Anderson TJ, Paermentier LA, Cutfield NJ, Chancellor AM, Mossman SS, Roxburgh RH.

Brain. 2014 Oct;137(Pt 10):2649-56. doi: 10.1093/brain/awu196. Epub 2014 Jul 28. Erratum in: Brain. 2015 Feb;138(Pt 2):e329.

PMID:
25070514
13.

Ophthalmic manifestations of inherited neurodegenerative disorders.

Kersten HM, Roxburgh RH, Danesh-Meyer HV.

Nat Rev Neurol. 2014 Jun;10(6):349-62. doi: 10.1038/nrneurol.2014.79. Epub 2014 May 20. Review.

PMID:
24840976
14.

Epiretinal membrane: a treatable cause of visual disability in myotonic dystrophy type 1.

Kersten HM, Roxburgh RH, Child N, Polkinghorne PJ, Frampton C, Danesh-Meyer HV.

J Neurol. 2014 Jan;261(1):37-44. doi: 10.1007/s00415-013-7141-6. Epub 2013 Oct 17.

PMID:
24132671
15.

Thrombo-embolic cerebral infarction secondary to giant Lambl's excrescence.

Wu TY, Gerber IL, Roxburgh RH.

J Clin Neurosci. 2013 Nov;20(11):1632-4. doi: 10.1016/j.jocn.2012.08.015. Epub 2013 May 11.

PMID:
23669170
16.

The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestry.

Roxburgh RH, Marquis-Nicholson R, Ashton F, George AM, Lea RA, Eccles D, Mossman S, Bird T, van Gassen KL, Kamsteeg EJ, Love DR.

J Neurol. 2013 May;260(5):1286-94. doi: 10.1007/s00415-012-6792-z. Epub 2012 Dec 27.

PMID:
23269439
17.

The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington disease.

Roxburgh RH, Smith CO, Lim JG, Bachman DF, Byrd E, Bird TD.

J Neurol Sci. 2013 Jan 15;324(1-2):176-8. doi: 10.1016/j.jns.2012.09.030. Epub 2012 Oct 17.

PMID:
23083689
18.

No evidence of a significant role for CTLA-4 in multiple sclerosis.

Roxburgh RH, Sawcer S, Maranian M, Seaman S, Hensiek A, Yeo T, Deans J, Compston A.

J Neuroimmunol. 2006 Feb;171(1-2):193-7. Epub 2005 Dec 1.

PMID:
16325273
19.

Japanese encephalitis acquired during travel in China.

Cutfield NJ, Anderson NE, Brickell K, Hueston L, Pikholz C, Roxburgh RH.

Intern Med J. 2005 Aug;35(8):497-8. No abstract available.

PMID:
16176476
20.

Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity.

Roxburgh RH, Seaman SR, Masterman T, Hensiek AE, Sawcer SJ, Vukusic S, Achiti I, Confavreux C, Coustans M, le Page E, Edan G, McDonnell GV, Hawkins S, Trojano M, Liguori M, Cocco E, Marrosu MG, Tesser F, Leone MA, Weber A, Zipp F, Miterski B, Epplen JT, Oturai A, Sørensen PS, Celius EG, Lara NT, Montalban X, Villoslada P, Silva AM, Marta M, Leite I, Dubois B, Rubio J, Butzkueven H, Kilpatrick T, Mycko MP, Selmaj KW, Rio ME, Sá M, Salemi G, Savettieri G, Hillert J, Compston DA.

Neurology. 2005 Apr 12;64(7):1144-51.

PMID:
15824338
21.

Recurrent Guillain-Barré syndrome.

Roxburgh RH, Young AC.

Br J Hosp Med. 1996 Oct 2-15;56(7):369-70. No abstract available.

PMID:
8899229

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