Byron Kakulas
Affiliations: | Perth, Perth, Western Australia, Australia |
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Sign in to add trainee| Frank L. Mastaglia | research scientist | ||
| Edward P. Richardson Jr. | research scientist | 1977-1977 | Perth |
| Edward P. Richardson Jr. | research scientist | 1987-1987 | Perth |
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Publications
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| Mastaglia FL, Byrnes ML, Johnsen RD, et al. (2003) Prevalence of cerebral vascular amyloid-beta deposition and stroke in an aging Australian population: a postmortem study. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 10: 186-9 |
| Mastaglia FL, Johnsen RD, Byrnes ML, et al. (2003) Prevalence of amyloid-beta deposition in the cerebral cortex in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 18: 81-6 |
| Mastaglia FL, Johnsen RD, Kakulas BA. (2002) Prevalence of stroke in Parkinson's disease: a postmortem study. Movement Disorders : Official Journal of the Movement Disorder Society. 17: 772-4 |
| Nowak KJ, Walsh P, Jacob RL, et al. (2000) Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion. Neuromuscular Disorders : Nmd. 10: 100-7 |
| Mastaglia FL, Nowak KJ, Stell R, et al. (1999) Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 174-9 |
| Mastaglia FL, Harker N, Phillips BA, et al. (1998) Dominantly inherited proximal myotonic myopathy and leukoencephalopathy in a family with an incidental CLCN1 mutation. Journal of Neurology, Neurosurgery, and Psychiatry. 64: 543-7 |
| Howell JM, Fletcher S, Kakulas BA, et al. (1997) Use of the dog model for Duchenne muscular dystrophy in gene therapy trials. Neuromuscular Disorders : Nmd. 7: 325-8 |
| Kakulas BA. (1997) Problems and potential for gene therapy in Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 7: 319-24 |
| Kwok JB, Taddei K, Hallupp M, et al. (1997) Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype. Neuroreport. 8: 1537-42 |
| Jongpiputvanich S, Walsh PJ, Kakulas BA. (1995) Minicores and congential fibre type disproportion observed in a family. Journal of Paediatrics and Child Health. 31: 253-7 |