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Personal profile


  • Cellular mechanisms of neurodegeneration
  • Clinical neuroscience
  • Genetics and treatment of Parkinson's disease
  • Genetic susceptibility factors in degenerative diseases of brain and muscles
  • Pathogenesis and treatment of inflammatory muscle diseases
  • Therapeutic brain stimulation

Fingerprint Dive into the research topics where Frank Mastaglia is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 15 Similar Profiles
Inclusion Body Myositis Medicine & Life Sciences
Parkinson Disease Medicine & Life Sciences
Transcranial Magnetic Stimulation Medicine & Life Sciences
Motor Evoked Potentials Medicine & Life Sciences
Muscles Medicine & Life Sciences
Myositis Medicine & Life Sciences
Motor Cortex Medicine & Life Sciences
Hand Medicine & Life Sciences

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Research Output 1968 2019

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
2 Citations (Scopus)

Elevated Serum Homocysteine Levels Have Differential Gender-Specific Associations with Motor and Cognitive States in Parkinson's Disease

Bakeberg, M. C., Jefferson, A., Riley, M., Byrnes, M., Ghosh, S., Mastaglia, F. L., Horne, M. K., McGregor, S., Stell, R., Kenna, J., Walters, S., Hince, D. & Anderton, R. S., 2019, In : Parkinson's Disease. 8 p., 3124295.

Research output: Contribution to journalArticle

Open Access

Imaging in the diagnosis of idiopathic inflammatory myopathies; indications and utility

Paramalingam, S., Counsel, P., Mastaglia, F. L., Keen, H. & Needham, M., 1 Feb 2019, In : Expert Review of Neurotherapeutics. 19, 2, p. 173-184 12 p.

Research output: Contribution to journalReview article

Expert Testimony
Diagnostic Imaging
Early Diagnosis

Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): Case reports and epidemiology of ETFDH gene mutations

Chen, W., Zhang, Y., Ni, Y., Cai, S., Zheng, X., Mastaglia, F. L. & Wu, J., 18 Dec 2019, In : BMC Neurology. 19, 1, 330.

Research output: Contribution to journalArticle

Open Access
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
7 Citations (Scopus)

Projects 1998 2012