• The University of Western Australia (M309), 35 Stirling Highway,

    6009 Perth


  • 595 Citations
  • 12 h-Index
1992 …2019
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Fingerprint Dive into the research topics where Anthony Akkari is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 10 Similar Profiles
Tropomyosin Medicine & Life Sciences
Baculoviridae Medicine & Life Sciences
Skeletal Muscle Medicine & Life Sciences
Genes Medicine & Life Sciences
Distal Myopathies Medicine & Life Sciences
Nemaline Myopathies Medicine & Life Sciences
Synucleins Medicine & Life Sciences
Chromosomes, Human, Pair 14 Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 1992 2019

  • 595 Citations
  • 12 h-Index
  • 16 Article
  • 6 Conference paper
  • 6 Other chapter contribution
  • 2 Review article

ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?

Mejzini, R., Flynn, L. L., Pitout, I. L., Fletcher, S., Wilton, S. D. & Akkari, P. A., 6 Dec 2019, In : Frontiers in Neuroscience. 13, 1310.

Research output: Contribution to journalReview article

Open Access
Amyotrophic Lateral Sclerosis
Research Personnel

Altered gut microbiome in Parkinson's disease and the influence of lipopolysaccharide in a human α-synuclein over-expressing mouse model

Gorecki, A. M., Preskey, L., Bakeberg, M. C., Kenna, J. E., Gildenhuys, C., MacDougall, G., Dunlop, S. A., Mastaglia, F. L., Anthony Akkari, P., Koengten, F. & Anderton, R. S., Aug 2019, In : Frontiers in Neuroscience. 13, JUL, 839.

Research output: Contribution to journalArticle

Open Access
Parkinson Disease
16S Ribosomal RNA
12 Citations (Scopus)

Translational development of splice-modifying antisense oligomers

Fletcher, S., Bellgard, M., Price, L., Akkari, A. & Wilton, S., 2 Jan 2017, In : Expert Opinion on Biological Therapy. 17, 1, p. 15-30 16 p.

Research output: Contribution to journalReview article

Spinal Muscular Atrophy
Duchenne Muscular Dystrophy
Patient Participation
42 Citations (Scopus)

An αtropomyosin mutation alters dimer preference in nemaline myopathy

Corbett, M. A., Akkari, P. A., Domazetovska, A., Cooper, S. T., North, K. N., Laing, N., Gunning, P. W. & Hardeman, E. C., 2005, In : Annals of Neurology. 57, 1, p. 42-49

Research output: Contribution to journalArticle

Nemaline Myopathies
Muscle Weakness
5 Citations (Scopus)
Affinity Chromatography

Projects 2003 2003