Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency.

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Leigh's Disease: The Acute Clinical Course of a Two-Year-Old Child with Subacute Necrotizing Encephalomyelopathy.Cranial ultrasound in metabolic disorders presenting in the neonatal period: characteristic features and comparison with MR imaging

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Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency.

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2001 nî lūn-bûn

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2001年の論文

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2001年学术文章

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2001年学术文章

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2001年学术文章

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2001年学术文章

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2001年学术文章

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2001年學術文章

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2001年學術文章

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2001年學術文章

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Leigh disease: clinical, neuro ...... tochrome c oxidase deficiency.

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Leigh disease: clinical, neuro ...... tochrome c oxidase deficiency.

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Leigh disease: clinical, neuro ...... tochrome c oxidase deficiency.

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Leigh disease: clinical, neuro ...... tochrome c oxidase deficiency.

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Leigh disease: clinical, neuro ...... tochrome c oxidase deficiency.

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Leigh disease: clinical, neuro ...... tochrome c oxidase deficiency.

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SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

Subacute necrotizing encephalomyelopathy in an infant

Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

Subacute necrotizing encephalomyelopathy. A review and a study of two families.

Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.

Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literature.

Disorders of movement in Leigh syndrome.

Pathogenic factors underlying the lesions in Leigh's disease. Tissue responses to cellular energy deprivation and their clinico-pathological consequences.

Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (Leigh disease).

A single cell complementation class is common to several cases of cytochrome c oxidase-defective Leigh's syndrome.

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608-613

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scholarly article

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10.1177/088307380101600816

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Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency.

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P2860

P2860

Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency.

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