| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1046113273 |
| P356 | DOI | 10.1038/EYE.2011.2 |
| P932 | PMC publication ID | 3094220 |
| P698 | PubMed publication ID | 21378995 |
| P5875 | ResearchGate publication ID | 50290140 |
| P50 | author | Patrick Yu-Wai-Man | Q28321954 |
| Patrick F. Chinnery | Q67217990 | ||
| P2093 | author name string | P G Griffiths | |
| A Atawan | |||
| M Bailie | |||
| P2860 | cites work | OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes | Q24304868 |
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| Multi-system neurological disease is common in patients with OPA1 mutations | Q24619312 | ||
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| Detection of glaucoma progression with stratus OCT retinal nerve fiber layer, optic nerve head, and macular thickness measurements | Q33509470 | ||
| The prevalence and natural history of dominant optic atrophy due to OPA1 mutations | Q33693684 | ||
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| Infliximab in serpiginous choroiditis | Q43267967 | ||
| Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance. | Q44306523 | ||
| Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy | Q45209829 | ||
| Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations | Q45209833 | ||
| Axonal loss occurs early in dominant optic atrophy | Q46080771 | ||
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| An investigation of the retinal nerve fibre layer in progressive multiple sclerosis using optical coherence tomography | Q46868407 | ||
| eOPA1: an online database for OPA1 mutations | Q48142349 | ||
| Histogenesis of the intravitreal membrane and secondary vitreous in the mouse. | Q50697248 | ||
| Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations. | Q51751759 | ||
| Reduction of inner retinal thickness in patients with autosomal dominant optic atrophy associated with OPA1 mutations. | Q53532046 | ||
| The natural history of OPA1-related autosomal dominant optic atrophy | Q56582242 | ||
| Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy | Q71814832 | ||
| Reproducibility of peripapillary retinal nerve fiber thickness measurements with stratus OCT in glaucomatous eyes | Q80811906 | ||
| Hereditary optic neuropathies | Q80981275 | ||
| P433 | issue | 5 | |
| P921 | main subject | retinal ganglion cell | Q927337 |
| optic atrophy | Q3629049 | ||
| P304 | page(s) | 596-602 | |
| P577 | publication date | 2011-03-04 | |
| P1433 | published in | Eye | Q10278937 |
| P1476 | title | Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations | |
| P478 | volume | 25 |
| Q28072026 | A neurodegenerative perspective on mitochondrial optic neuropathies |
| Q50074079 | Characterization of Charcot-Marie-Tooth optic neuropathy. |
| Q91133950 | Clinical utility gene card for: inherited optic neuropathies including next-generation sequencing-based approaches |
| Q42286795 | Complex I inhibition in the visual pathway induces disorganization of the node of Ranvier |
| Q98943954 | Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report |
| Q38605002 | Diagnostic genetic testing for patients with bilateral optic neuropathy and comparison of clinical features according to OPA1 mutation status |
| Q35928805 | Disorders of the optic nerve in mitochondrial cytopathies: new ideas on pathogenesis and therapeutic targets |
| Q38285228 | Disturbed mitochondrial dynamics and neurodegenerative disorders |
| Q30459784 | Dominant optic atrophy. |
| Q26752831 | Genetic manipulation for inherited neurodegenerative diseases: myth or reality? |
| Q40523875 | Genotype-phenotype heterogeneity of ganglion cell and inner plexiform layer deficit in autosomal-dominant optic atrophy |
| Q35221288 | Homocysteine-mediated modulation of mitochondrial dynamics in retinal ganglion cells |
| Q37625339 | Mitochondrial Dynamics in Retinal Ganglion Cell Axon Regeneration and Growth Cone Guidance |
| Q36358765 | Mitochondrial dynamics regulate growth cone motility, guidance, and neurite growth rate in perinatal retinal ganglion cells in vitro. |
| Q36439203 | Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets |
| Q27009498 | OCT: New perspectives in neuro-ophthalmology |
| Q86018970 | Optical coherence tomography shows early loss of the inferior temporal quadrant retinal nerve fiber layer in autosomal dominant optic atrophy |
| Q45483589 | Physiological evidence for impairment in autosomal dominant optic atrophy at the pre-ganglion level |
| Q43116350 | Reply: Sensorineural hearing loss in OPA1-linked disorders |
| Q42739188 | Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation |
| Q42581056 | SDOCT thickness measurements of various retinal layers in patients with autosomal dominant optic atrophy due to OPA1 mutations |
| Q50726746 | Selective retinal ganglion cell loss in familial dysautonomia. |
| Q36315354 | Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy |
| Q37616208 | The Pattern of Retinal Ganglion Cell Loss in OPA1-Related Autosomal Dominant Optic Atrophy Inferred From Temporal, Spatial, and Chromatic Sensitivity Losses |
| Q47677362 | Thickness mapping of individual retinal layers and sectors by Spectralis SD-OCT in Autosomal Dominant Optic Atrophy. |
| Q38040328 | Treatment of hereditary optic neuropathies |
| Q33595163 | Treatment strategies for inherited optic neuropathies: past, present and future |
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