26 results on '"Sue, Carolyn M."'
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2. 3.
3. 43.
4. 62. Rotenone toxicity in parkin mutated olfactory cell cultures
5. 55. Mutations in PARK9 (ATP13A2) causing Kufor-Rakeb syndrome, provide insights into cellular dysfunction in Parkinson’s disease
6. 70. A case series of intra-arterial embolectomy for acute ischemic stroke
7. 56. Mitochondrial abnormalities in a new cell model of MNGIE syndrome
8. 57. Benign infantile cytochrome c oxidase deficiency myopathy: Reversible or not?
9. 215. Pathogenic effects of novel mutations in ATP13A2 (PARK9) Causing Kufor-Rakeb Syndrome, an Autosomal Recessive Form of Early-onset Parkinsonism
10. 222. Mutation Analysis of Spastin (SPG4) in Patients with Hereditary Spastic Paraplegia
11. 227. Leber‘s hereditary optic neuropathy associated with multiple sclerosis
12. 412: Measurement of clinical severity in patients with mitochondrial disease
13. 422: Abnormalities of gastrointestinal transit in MELAS syndrome
14. 439: Detection of large-scale deletions in mitochondrial DNA using DNA extracted from salivary samples
15. 410: Autosomal dominant late-onset Parkinson’s disease due to a novel A1442P mutation in the LRRK2 gene
16. 411: Hsp60 gene mutations in patients with hereditary spastic paraplegia: A pilot study
17. 409: Efficient screening method for PINK1 gene mutations using DHPLC
18. 642: Population prevalence of patients with Parkinson’s disease in the Australian community
19. 634: ATP synthesis and apoptosis in mitochondrial disorders
20. 308: Olfactory stem cells can be used as cell model for neurological disease
21. 625: Mitochondrial DNA A1555G point mutation and age-related hearing loss
22. 307: Prevalence of LRRK2 mutations in Australians with Parkinson’s Disease
23. 63.: Cortical dysfunction in hereditary spastic paraparesis patients with the spastin mutation
24. 43.: Mitochondrial dysfunction in PINK1 mutant human olfactory neurospheres is rescued by overexpression of PGC-1a
25. 3.: Microtubule dysfunction in whispering dysphonia (DYT4 dystonia)
26. 117. Clinical, neurophysiological and genetic observations in kufor-rakeb syndrome: report of a new kindred with compound heterozygous mutations in the ATP13A2 Gene.
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