26 results on '"Sue, Carolyn M."'
Search Results
2. The pathogenesis of Parkinson's disease
3. Mitochondrial disease in adults: recent advances and future promise
4. Depression in Parkinson's disease: Perspectives from an Australian cohort
5. Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes
6. Outcome measures for hereditary spastic paraplegia clinical trials: Learnings from an Australian HSP center
7. Maximizing benefits of the levodopa/carbidopa intestinal gel: Systematic considerations, challenging convention and individualizing approaches
8. Loss of ATP13A2 impairs glycolytic function in Kufor-Rakeb syndrome patient-derived cell models
9. Functional hyperspectral imaging captures subtle details of cell metabolism in olfactory neurosphere cells, disease-specific models of neurodegenerative disorders
10. Systematic review of cardiac electrical disease in Kearns–Sayre syndrome and mitochondrial cytopathy
11. Peripheral neuropathy in hereditary spastic paraplegia due to spastin (SPG4) mutation – A neurophysiological study using excitability techniques
12. The commercial genetic testing landscape for Parkinson's disease
13. Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings
14. Generation of human-induced pluripotent-stem-cell-derived cortical neurons for high-throughput imaging of neurite morphology and neuron maturation
15. ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome
16. Infantile encephalopathy associated with the MELAS A3243G mutation
17. The gut microbiota: A novel therapeutic target in Parkinson's disease?
18. Olfactory Impairment in Older Adults Is Associated With Depressive Symptoms and Poorer Quality of Life Scores
19. 63.: Cortical dysfunction in hereditary spastic paraparesis patients with the spastin mutation
20. 43.: Mitochondrial dysfunction in PINK1 mutant human olfactory neurospheres is rescued by overexpression of PGC-1a
21. 3.: Microtubule dysfunction in whispering dysphonia (DYT4 dystonia)
22. 642: Population prevalence of patients with Parkinson’s disease in the Australian community
23. 634: ATP synthesis and apoptosis in mitochondrial disorders
24. 625: Mitochondrial DNA A1555G point mutation and age-related hearing loss
25. 308: Olfactory stem cells can be used as cell model for neurological disease
26. 307: Prevalence of LRRK2 mutations in Australians with Parkinson’s Disease
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