| case report | Q2782326 |
| scholarly article | Q13442814 |
| P2093 | author name string | Bettina Zinka | |
| Matthias Graw | |||
| Andreas Buettner | |||
| P2860 | cites work | Subacute necrotizing encephalomyelopathy in an infant | Q24564004 |
| Atypical presentations of leigh syndrome: a case series and review | Q30988726 | ||
| A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethality. | Q34295052 | ||
| Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency | Q42508837 | ||
| Cytochrome c oxidase partial deficiency-associated Leigh disease presenting as an extrapyramidal syndrome | Q42508840 | ||
| Leigh's syndrome | Q45169012 | ||
| MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome | Q46186157 | ||
| Mitochondrial diseases in children including Leigh syndrome--biochemical and molecular background | Q46353939 | ||
| [Newborn infant with cerebral symptoms. Leigh disease] | Q71797875 | ||
| [Adult Leigh syndrome. A rare differential diagnosis of central respiratory insufficiency] | Q72153664 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P304 | page(s) | 986302 | |
| P577 | publication date | 2010-06-10 | |
| P1433 | published in | Case Reports in Medicine | Q26853852 |
| P1476 | title | Leigh's Disease: The Acute Clinical Course of a Two-Year-Old Child with Subacute Necrotizing Encephalomyelopathy | |
| P478 | volume | 2010 |
| Q83229779 | Defined neuronal populations drive fatal phenotype in a mouse model of Leigh syndrome | cites work | P2860 |
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