442 results on '"Howell, Neil"'
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2. Metabolic support in left ventricular hypertrophy
3. Mutations in Mitochondrial Cytochrome c Oxidase Genes Segregate with Late-Onset Alzheimer Disease
4. Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?
5. National administrative data produces an accurate and stable risk prediction model for short-term and 1-year mortality following cardiac surgery
6. Discontinuation of Aspirin in Heartmate 3 Left Ventricular Assist Device
7. MtDNA population variation in Myalgic encephalomyelitis/Chronic fatigue syndrome in two populations: a study of mildly deleterious variants
8. Cardiogenic Shock Due to End-Stage Heart Failure and Acute Myocardial Infarction: Characteristics and Outcome of Temporary Mechanical Circulatory Support
9. The effect of left ventricular assist device therapy in patients with heart failure and mixed pulmonary hypertension
10. Surgical management of left ventricular outflow obstruction in hypertrophic cardiomyopathy
11. Mitochondrial Dysfunction and Alzheimer’s Disease
12. Establishing risk of vision loss in Leber hereditary optic neuropathy
13. Patient-Prosthesis Mismatch in Patients With Aortic Stenosis Undergoing Isolated Aortic Valve Replacement Does Not Affect Survival
14. Ventricular assist device: destination UK
15. Cytoplasmic Transfer of DNA Containing Simian Virus 40 Sequences into Mouse 3T3 Cells
16. Planning Resources for Children in Care
17. The Geographical Allocation of Community Care Resources -- A Case Study
18. Mitochondrial Biogenesis in Neurospora crassa: I. An Ultrastructural and Biochemical Investigation of the Effects of Anaerobiosis and Chloramphenicol Inhibition
19. Relationship between plasma, atrial and ventricular perhexiline concentrations in humans: insights into factors affecting myocardial uptake
20. Coronary Ostial Compromise in Aortic Valve Replacement: A Rare But Avoidable Fatal Complication
21. Does the mitochondrial genome play a role in the etiology of Alzheimer’s disease?
22. Clinical expression of Leber Heredity Optic Neuropathy is affected by the mitochondrial DNA-haplogroup background
23. The Value of Lung Injury Score in Assessing the Outcome of Patients with Rib Fracture
24. Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigree
25. The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event
26. Mitochondrial DNA and survival after sepsis: a prospective study
27. Comparative genomics and the evolution of human mitochondrial DNA: assessing the effects of selection
28. Reply to the Editor
29. Putting the record straight on aprotinin as safe and effective: Results from a mixed treatment meta-analysis of trials of aprotinin
30. Origin and diffusion of mtDNA haplogroup X
31. Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy
32. The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates
33. Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups
34. Leber Hereditary Optic Neuropathy: How Do Mitochondrial DNA Mutations Cause Degeneration of the Optic Nerve?
35. Bleeding in cardiac surgery: The use of aprotinin does not affect survival
36. Pathogenic mitochondrial DNA mutations in genes that encode respiratory chain subunits
37. Relative Rates of Evolution in the Coding and Control Regions of African mtDNAs
38. mtDNA mutations that cause optic neuropathy: how do we know?
39. Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain
40. Development of 17α-Estradiol as a Neuroprotective Therapeutic Agent: Rationale and Results from a Phase I Clinical Study
41. Mitochondrial gene segregation in mammals: is the bottleneck always narrow?
42. African Haplogroup L mtDNA Sequences Show Violations of Clock-like Evolution
43. Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees
44. Electrochemical and spectral analysis of the long-range interactions between the Qo and Qi sites and the heme prosthetic groups in ubiquinol-cytochrome c oxidoreductase
45. Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene
46. Human Mitochondrial Diseases: Answering Questions and Questioning Answers
47. Restoring energy in a power crisis: mitochondrial targets for drug development
48. Mitochondrial DNA analysis: polymorphisms and pathogenicity
49. Clinical mitochondrial genetics
50. Metabolic Profiling of Aortic Stenosis and Hypertrophic Cardiomyopathy Identifies Mechanistic Contrasts in Substrate Utilisation
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