22 results on '"Carelli V."'
Search Results
2. Radon in indoor air of primary schools: a systematic survey to evaluate factors affecting radon concentration levels and their variability
3. Narcolepsy marks DNMT1-associated disorders: EP3264
4. Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?
5. Optic nerve and melanopsin retinal ganglion cells involvement in relation to circadian dysfunction in Alzheimer’s disease: O331
6. Secondary headache in children
7. Multi-system neurological disease is common in patients with OPA1 mutations
8. Pathophysiology of mitochondrial optic neuropathies: are LHON and DOA a variation on the same theme?: 3311
9. Choline pivaloyl ester strengthened the benefit effects of Tacrine and Galantamine on electroencephalographic and cognitive performances in nucleus basalis magnocellularis-lesioned and aged rats
10. The 13042G→A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype
11. The role of mitochondria in health, ageing, and diseases affecting vision
12. Colour vision defects in asymptomatic carriers of the Leber’s hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study
13. Caspase-independent death of Leberʼs hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G
14. Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber’s hereditary optic neuropathy
15. Correlation between retinal nerve fibre layer thickness and optic nerve head size: an optical coherence tomography study
16. Matrices for site-specific controlled-delivery of 5-fluorouracil to descending colon
17. Dominance in mitochondrial disorders
18. Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leberʼs hereditary optic neuropathy
19. Leberʼs hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases
20. Familial Colpocephaly, Corpus Callosum Hypogenesis, Visual Failure, and Epilepsy.
21. Familial Epileptic Encephalopathy and Optic Atrophy Harboring an mtDNA Haplotype Associated with Leber's Hereditary Optic Neuropathy
22. Lack of association between mitochondrial tRNA (Leu)(UUR) point mutation and cluster headache
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