Centre for Neuromuscular & Neurological Disorders

Research Output 1979 2019

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Letter
2016

Acute reversible seronegative cerebellar ataxia in a young woman with ovarian teratoma

Yau, W. Y., Fabis-Pedrini, M. J. & Kermode, A. G., 15 Oct 2016, In : Journal of the Neurological Sciences. 369, p. 227-228 2 p.

Research output: Contribution to journalLetter

10 Citations (Scopus)

Revising the ICD: stroke is a brain disease

Shakir, R., Davis, S., Norrving, B., Grisold, W., Carroll, W. M., Feigin, V. L. & Hachinski, V., 19 Nov 2016, In : The Lancet. 388, 10059, p. 2475-2476 2 p.

Research output: Contribution to journalLetter

6 Citations (Scopus)
2015
24 Citations (Scopus)

Helicobacter pylori infection as a protective factor against multiple sclerosis risk in females

Pedrini, M., Seewann-Gaitatzis, A., Bennett, K. A., Wood, A., James, I., Burton, J., Marshall, B., Carroll, B. & Kermode, A., Jun 2015, In : Journal of Neurology, Neurosurgery and Psychiatry. 86, 6, p. 603-607

Research output: Contribution to journalLetter

Open Access
Helicobacter Infections
Helicobacter pylori
Multiple Sclerosis
Hygiene Hypothesis
Parturition
2014
3 Citations (Scopus)

Pre-hospital stroke management: An Australian perspective

Blacker, D. & Hankey, G., Dec 2014, In : Internal Medicine Journal. 44, 12, p. 1151-1153

Research output: Contribution to journalLetter

Open Access
1 Citation (Scopus)

Reply: Evidence against volume conduction to explain normal MEPs in muscles with low motor power in SCI

Edwards, D., Cortés, M. L., Thickbroom, G., Rykman, A., Pascual- Leone, A. M. & Volpe, B. T., 2014, In : Spinal Cord. 52, 9, p. 1

Research output: Contribution to journalLetter

2013
602 Citations (Scopus)

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Beecham, A. H., Patsopoulos, N. A., Xifara, D. K., Davis, M. F., Kemppinen, A., Cotsapas, C. J., Shah, T. S., Spencer, C. C. A., Booth, D. R., Goris, A. N., Oturai, A. B., Saarela, J., Fontaine, B., Hemmer, B., Martin, C. F. C., Zipp, F., D'Alfonso, S., Martinelli-Boneschi, F., Taylor, B. V., Harbo, H. F. & 173 othersKockum, I., Hillert, J., Olsson, T. P., Ban, M., Oksenberg, J. R., Hintzen, R. Q., Barcellos, L. F., Agliardi, C., Alfredsson, L. S., Alizadeh, M., Anderson, C. A., Andrews, R., Søndergaard, H. B., Baker, A. P., Band, G., Baranzini, S. E., Barizzone, N., Barrett, J. C., Bellenguez, C., Bergamaschi, L., Bernardinelli, L., Berthele, A., Biberacher, V., Binder, T. M. C., Blackburn, H., Bomfim, I. L., Brambilla, P., Broadley, S. A., Brochet, B., Brundin, L., Buck, D., Butzkueven, H., Caillier, S. J., Camu, W., Carpentier, W., Cavalla, P., Celius, E. G., Coman, I., Comi, G., Corrado, L., Cosemans, L., Cournu-Rebeix, I., Cree, B. A. C., Cusi, D., Damotte, V., Defer, G. L., Delgado, S. R., Deloukas, P., Di Sapio, A., Dilthey, A. T., Donnelly, P. K., Dubois, B. D., Duddy, M. E., Edkins, S. J., Elovaara, I., Esposito, F., Evangelou, N., Fiddes, B., Field, J. G., Franke, A., Freeman, C. O., Frohlich, I. Y., Galimberti, D., Gieger, C., Gourraud, P. A. F. D., Graetz, C., Graham, A., Grummel, V., Guaschino, C., Hadjixenofontos, A., Hákonarson, H. H., Halfpenny, C. A., Hall, G., Hall, P., Hamsten, A., Harley, J., Harrower, T. P., Hawkins, C. P., Hellenthal, G., Hillier, C. E. M., Hobart, J. C., Hoshi, M., Hunt, S. E., Jagodić, M., Jelčić, I., Jochim, A., Kendall, B., Kermode, A., Kilpatrick, T. J., Koivisto, K. J., Konidari, I., Korn, T., Kronsbein, H. C., Langford, C., Larsson, M., Lathrop, M. G., Lebrun-Frénay, C., Lechner-Scott, J. S., Lee, M., Leone, M. A., Leppä, V., Liberatore, G., Lie, B. A., Lill, C. M., Lindén, M., Link, J., Luessi, F., Lycke, J. N., Macciardi, F. M., Männistö, S., Manrique, C. P., Martin, R., Martinelli, V., Mason, D. M. L., Mazibrada, G., Mccabe, C., Mero, I. L., Mescheriakova, J., Moutsianas, L., Myhr, K. M., Nagels, G., Nicholas, R. S. J., Nilsson, P. C., Piehl, F., Pirinen, M., Price, S. E., Quach, H. L., Reunanen, M. I., Robberecht, W., Robertson, N. P., Rodegher, M. E., Rog, D. J., Salvetti, M., Schnetz-Boutaud, N. C., Sellebjerg, F. T., Selter, R. C., Schaefer, C. A., Shaunak, S., Shen, L., Shields, S., Siffrin, V., Slee, M., Sørensen, P. S., Sorosina, M., Sospedra, M., Spurkland, A., Strange, A., Sundqvist, E., Thijs, V. N. S., Thorpe, J. W., Ticca, A. F., Tienari, P. J., Van Duijn, C. M. A., Visser, E. M., Vucic, S., Westerlind, H., Wiley, J. S., Wilkins, A., Wilson, J. F., Winkelmann, J., Zajicek, J. P., Zindler, E., Haines, J. L., Pericak-Vance, M. A., Ivinson, A. J., Stewart, G. J., Hafler, D. D., Hauser, S. L., Compston, A. D., Mcvean, G. A. T., De Jager, P. L., Sawcer, S. J. & Mccauley, J. L., 2013, In : Nature Genetics. 45, 11, p. 1353-1362

Research output: Contribution to journalLetter

Multiple Sclerosis
Genome-Wide Association Study
Major Histocompatibility Complex

Reply

Mcauliffe, W. & Kermode, A., 2013, In : American Journal of Neuroradiology. 34, p. E71

Research output: Contribution to journalLetter

Open Access
9 Citations (Scopus)

Translating the genomics revolution: The need for an international gene therapy consortium for monogenic diseases

Tremblay, J. P., Xiao, X., Aartsma-Rus, A. M., Barbas, C., Blau, H. M., Bogdanove, A. J., Boycott, K. M., Braun, S., Breakefield, X. O., Bueren, J. A., Buschmann, M. D., Byrne, B. J., Calos, M. P., Cathomen, T., Chamberlain, J. S., Chuah, M., Cornetta, K. G., Davies, K. E., Dickson, J. G., Duchateáu, P. N. & 30 othersFlotte, T. R., Gaudet, D., Gersbach, C. A., Gilbert, R., Glorioso, J. C., Herzog, R. W., High, K. A., Huang, W., Huard, J., Joung, J. K., Liu, D., Lochmüller, H., Lustig, L. R., Martens, J. R., Massie, B., Mavilio, F., Mendell, J. R., Nathwani, A. C., Ponder, K. P., Porteus, M. H., Puymirat, J., Samulski, R. J. S., Takeda, S., Thrasher, A. J., Vandendriessche, T. C., Wei, Y., Wilson, J. M., Wilton, S., Wolfe, J. H. & Gao, G., 2013, In : Molecular Therapy. 21, 2, p. 266-268

Research output: Contribution to journalLetter

Open Access
2012
1 Citation (Scopus)

Extreme Task Specificity: Is It Dystonia or Another Form of Motor Programming Abnormality?

Lang, A. E., Prashanth, L. K., Ghosh, S., Elahi, B. & Ghen, R., 2012, In : Movement Disorders. 27, 9, p. 1198-1199

Research output: Contribution to journalLetter

2009
11 Citations (Scopus)
Open Access
Robotics
Rehabilitation
Brain
Learning
Evidence-Based Medicine
2008

Exon skipping in Duchenne muscular dystrophy

Wilton, S., 2008, In : Neuromuscular Disorders. 18, p. 431-432

Research output: Contribution to journalLetter

1 Citation (Scopus)

Personal reflections on the neuropathology of kuru

Kakulas, B., 2008, In : PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES. 363, 1510, p. 3645-3646

Research output: Contribution to journalLetter

Open Access
2005
16 Citations (Scopus)

In reply to J Silver

Kakulas, B., 2005, In : Spinal Cord. 43, p. 327

Research output: Contribution to journalLetter

2004
8 Citations (Scopus)
2001
5 Citations (Scopus)

Craniocervical tetanus presenting with dysphagia:Diagnostic value of elecrophysiological studies

Mastaglia, F., Thickbroom, G., Day, T. & Bond, R., 2001, In : Journal of Neurology. 248, p. 903-904

Research output: Contribution to journalLetter

2000

Inclusion body myositis

Mastaglia, F., 2000, In : World Neurology. 15, 4, p. 9-10

Research output: Contribution to journalLetter

1999
8 Citations (Scopus)

Relapses in idiopathic inflammatory myopathies

Mastaglia, F., Phillips, B. A., Zilko, P. J. & Garlepp, M. J., 1999, In : Muscle and Nerve. 22, p. 1161-1162

Research output: Contribution to journalLetter

48 Citations (Scopus)

The alpha-synuclein gene is not a major risk factor in familial Parkinson's disease

Scott, W. K., Yamoaka, L. H., Stajich, J. M., Scott, B. L., Vance, J. M., Roses, A. D., Pericak-Vance, M. A., Watts, R. L., Nance, M., Hubble, J., Koller, W., Stern, M. B., Colcher, A., Allen Jr, F. H., Hiner, B. C., Jankovic, J., Ondo, W., Laing, N., Mastaglia, F., Goetz, C. & 5 othersPappert, E., Small, G. W., Masterman, D., Haines, J. L. & Davies, T. L., 1999, In : Neurogenetics. 2, p. 191-192

Research output: Contribution to journalLetter

1998
18 Citations (Scopus)

Topical tretinoin and fetal malformations

Colley, S. M. J., Walpole, I., Fabian, V. A. & Kakulas, B., 1998, In : Medical Journal of Australia. 168, 4, May, p. 467

Research output: Contribution to journalLetter

1996
24 Citations (Scopus)

Apolipoprotein E alleles in sporadic inclusion body myositis and hereditary inclusion body myositis

Garlepp, M. J. & Mastaglia, F., 1996, In : Annals of Neurology. 40, N/A, p. 264-265

Research output: Contribution to journalLetter

2 Citations (Scopus)

Apolipoprotein E and inclusion body myositis

Garlepp, M. J. & Mastaglia, F., 1996, In : Annals of Neurology. 40, 6, p. 826-828

Research output: Contribution to journalLetter

40 Citations (Scopus)

Apolipoprotein-E genotyping in diagnosis of Alzheimer's disease

Kakulas, B., Wilton, S., Fabian, V. A. & Jones, T. M., 1996, In : The Lancet. 348, 9025, p. 483

Research output: Contribution to journalLetter

5 Citations (Scopus)

Characterisation of the chicken Cu,Zn superoxide dismutase gene

Stanton, J. L., Wilton, S. & Laing, N., 1996, In : DNA Sequence. 6, p. 357-360

Research output: Contribution to journalLetter

Chickens
Genes
Xenopus laevis
DNA Sequence Analysis
Spinal Cord
24 Citations (Scopus)

Letter to Editor

Garlepp, M. J. & Mastaglia, F., 1996, In : Annals of Neurology. 40, 2, p. 264-265

Research output: Contribution to journalLetter

4 Citations (Scopus)

Long-range PCR: synthesis of products independent of size

Wilton, S. & Lim, L., 1996, In : Trends in Genetics. 12, p. 458

Research output: Contribution to journalLetter

2 Citations (Scopus)

Neuromuscular diseases: muscle

Kakulas, B., 1996, In : Current Opinion in Neurology. 9, p. 367-368

Research output: Contribution to journalLetter

1995
14 Citations (Scopus)
1994
2 Citations (Scopus)

Dystrophin in rimmed vacuoles

Nakazato, O., Johnsen, R., Morling, P. & Kakulas, B., 1994, In : Muscle and Nerve. 17, February, p. 252-253

Research output: Contribution to journalLetter

7 Citations (Scopus)

Enterovirus hypothesis for motor neurone disease

Swanson, N., Fox, S. A. & Mastaglia, F., 1994, In : BMJ: British Medical Journal. 309, p. 743

Research output: Contribution to journalLetter

45 Citations (Scopus)

Sporadic motor neurone disease due to a familial SOD1 mutation with low penetrance

Suthers, G., Laing, N., Wilton, S., Dorosz, S. & Waddy, H., 1994, In : Lancet. 344, p. 1773

Research output: Contribution to journalLetter

1992

Cortical activity preceeding self-initiated and externally triggered voluntary movement

Thickbroom, G. & Mastaglia, F., 1992, In : Movement Disorders. 7, 4, p. 390-390

Research output: Contribution to journalLetter

25 Citations (Scopus)

Intravenous immunoglobulin for multifocal motor neuropathy

Kermode, A. G., Laing, B. A., Carroll, W. M. & Mastaglia, F., 1992, In : The Lancet. 340, p. 920-921

Research output: Contribution to journalLetter