| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0967-5868(96)90063-6 |
| P698 | PubMed publication ID | 18638883 |
| P2093 | author name string | S J Read | |
| M P Pender | |||
| J D Harrison | |||
| P2860 | cites work | Multiple sclerosis presenting with progressive visual failure | Q33620218 |
| Autoimmune optic neuropathy: evaluation and treatment | Q33630496 | ||
| New diagnostic criteria for multiple sclerosis: guidelines for research protocols | Q34271601 | ||
| Connective tissue disease mimicking multiple sclerosis | Q38434863 | ||
| Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis | Q44557768 | ||
| Primary Sjögren's syndrome with central nervous system disease mimicking multiple sclerosis | Q48369443 | ||
| Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation | Q48450898 | ||
| The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation | Q48706853 | ||
| A collagen disorder of the nervous system presenting as multiple sclerosis. | Q51114814 | ||
| Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation | Q67588111 | ||
| Autoimmunity in multiple sclerosis | Q68278584 | ||
| Optic neuropathy in systemic lupus erythematosus | Q70025996 | ||
| Antinuclear antibodies in multiple sclerosis | Q70251695 | ||
| Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation | Q70655012 | ||
| Association of the 11778 mitochondrial DNA mutation and demyelinating disease | Q72643592 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 264-267 | |
| P577 | publication date | 1996-07-01 | |
| P1433 | published in | Journal of Clinical Neuroscience | Q6294963 |
| P1476 | title | Progressive visual loss: an unusual presentation of multiple sclerosis | |
| P478 | volume | 3 |
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