(Q33759088)

29 July 2017

1 reference

title

Mitochondrial respiratory chain disorders and the liver (English)

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29 July 2017

Morris AA

1

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29 July 2017

publication date

1 October 1999

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29 July 2017

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29 July 2017

volume

19

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29 July 2017

issue

5

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29 July 2017

page(s)

357-368

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Oxidative phosphorylation at the fin de siècle

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

21 January 2018

Mitochondrial evolution

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Molecular genetic aspects of human mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Hepatic failure and lactic acidosis due to fialuridine (FIAU), an investigational nucleoside analogue for chronic hepatitis B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Mitochondrial DNA polymerase gamma deficiency and mtDNA depletion in a child with Alpers' syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Early childhood hepatocerebral degeneration misdiagnosed as valproate hepatotoxicity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Fatal infantile liver failure associated with mitochondrial DNA depletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.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/10.1111%2FJ.1478-3231.1999.TB00063.X

Infantile Diffuse Cerebral Degeneration With Hepatic Cirrhosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Liver involvement in Alpers disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

The treatment of congenital lactic acidoses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Mitochondrial genetics '98 is the bottleneck cracked?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Hepatic failure in disorders of oxidative phosphorylation with neonatal onset

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Mitochondrial DNA rearrangements with onset as chronic diarrhea with villous atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

Prenatal diagnosis of systemic disorders of the respiratory chain in cultured chorionic villus fibroblasts by study of ATP-synthesis in digitonin-permeabilized cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

31P NMR examination of two patients with NADH-CoQ reductase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00063.X

10.1111/J.1478-3231.1999.TB00063.X

21 January 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference