27 results on '"Turnbull, Douglass M."'
Search Results
2. Mitochondrial Abnormality Associates with Type-Specific Neuronal Loss and Cell Morphology Changes in the Pedunculopontine Nucleus in Parkinson Disease
3. Defining cardiac adaptations and safety of endurance training in patients with m.3243A>G-related mitochondrial disease
4. A neurological perspective on mitochondrial disease
5. Mitochondrial medicine: A metabolic perspective on the pathology of oxidative phosphorylation disorders
6. Mitochondrial DNA and survival after sepsis: a prospective study
7. Childhood neurological presentation of a novel mitochondrial tRNA Val gene mutation
8. The neurology of mitochondrial DNA disease
9. A high frequency of mtDNA polymorphisms in HeLa cell sublines
10. The mitochondrial genome and mitochondrial muscle disorders
11. An antigenomic strategy for treating heteroplasmic mtDNA disorders
12. Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load
13. A novel mitochondrial tRNA Glu ( MTTE) gene mutation causing chronic progressive external ophthalmoplegia at low levels of heteroplasmy in muscle
14. Neuromuscular disease presentation with three genetic defects involving two genomes
15. A multiplex real-time PCR method to detect and quantify mitochondrial DNA deletions in individual cells
16. Distal weakness with respiratory insufficiency caused by the m.8344A > G “MERRF” mutation
17. Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?
18. Searching for the needle in the Haystacks
19. Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain
20. Mitochondrial DNA and disease
21. Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): A clinical, biochemical and molecular study
22. Measurement of the activity of individual respiratory chain complexes in isolated fibroblast mitochondria
23. Organic aciduria in fasted rats caused by 2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate (etomoxir)
24. 27 - Identification of Mitochondrial Dysfunction at Coupling Site II
25. 4 - Study of Skeletal Muscle Mitochondrial Dysfunction
26. Chapter 88 - Metabolic Myopathies (Including Mitochondrial Diseases)
27. Vomiting, anorexia, and mitochondrial DNA disease
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