(Q34063889)

30 July 2017

1 reference

title

Mitochondrial encephalomyopathy. (English)

1 reference

30 July 2017

Goto Y

1

1 reference

30 July 2017

1 September 2000

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30 July 2017

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30 July 2017

20 Suppl

1 reference

30 July 2017

S82-4

1 reference

A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

30 July 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

BCL-2 family members and the mitochondria in apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1789.2000.00304.X

10.1046/J.1440-1789.2000.00304.X

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference

PubMed ID

11037195