Childhood-Onset Progressive Dystonia With Mitochondrial DNA G14459A Mutation: Efficacy of Long-Term Sodium Succinate Treatment.

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Childhood-Onset Progressive Dystonia With Mitochondrial DNA G14459A Mutation: Efficacy of Long-Term Sodium Succinate Treatment.

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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Childhood-Onset Progressive Dy ...... rm Sodium Succinate Treatment.

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Childhood-Onset Progressive Dy ...... rm Sodium Succinate Treatment.

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label

Childhood-Onset Progressive Dy ...... rm Sodium Succinate Treatment.

@en

Childhood-Onset Progressive Dy ...... rm Sodium Succinate Treatment.

@nl

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Childhood-Onset Progressive Dy ...... rm Sodium Succinate Treatment.

@en

Childhood-Onset Progressive Dy ...... rm Sodium Succinate Treatment.

@nl

P1476

Childhood-Onset Progressive Dy ...... rm Sodium Succinate Treatment.

@en

P2093

Ayaka Koide

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Hiroshi Ozawa

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Masaya Kubota

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Yuichi Goto

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P2860

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

Pediatric-onset dystonia associated with bilateral striatal necrosis and G14459A mutation in a Korean family: a case report.

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.

Persistent diffusion abnormalities in the brain stem of three children with mitochondrial diseases.

Successful treatment with succinate in a patient with MELAS.

Leber's hereditary optic neuropathy with dystonia in a Japanese family.

Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy.

Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation.

P304

2329048X14550677

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scholarly article

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10.1177/2329048X14550677

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P433

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P478

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P577

2014-07-01T00:00:00Z

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P5875

285316391

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P698

28503583

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P921

mitochondrial DNA

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5388318

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