(Q51718920)

10 April 2018

title

Progressive reversion of clinical and molecular phenotype in a child with liver mitochondrial DNA depletion. (English)

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10 April 2018

main subject

mitochondrial DNA

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author name string

Pierre-Henri Ducluzeau

1

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10 April 2018

Alain Lachaux

2

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10 April 2018

Raymonde Bouvier

3

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10 April 2018

Hervé Duborjal

4

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10 April 2018

Georges Stepien

5

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10 April 2018

Dominique Bozon

6

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10 April 2018

Bénédicte Mousson de Camaret

7

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10 April 2018

publication date

1 May 2002

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10 April 2018

published in

Journal of Hepatology

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10 April 2018

volume

36

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10 April 2018

issue

5

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10 April 2018

page(s)

698-703

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10 April 2018

Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900021-1

7 January 2021

Clinical manifestations of mitochondrial DNA depletion

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Mitochondrial DNA depletion in a patient with long survival

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7 January 2021

Clinical heterogeneity associated with mitochondrial DNA depletion in muscle

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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900021-1

7 January 2021

Fatal infantile liver failure associated with mitochondrial DNA depletion

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900021-1

7 January 2021

Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease

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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900021-1

7 January 2021

Liver failure associated with mitochondrial DNA depletion

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7 January 2021

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

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7 January 2021

Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy

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7 January 2021

Depletion of mitochondrial DNA associated with infantile cholestasis and progressive liver fibrosis.

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7 January 2021

Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts

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7 January 2021

Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylation

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7 January 2021

Molecular mechanisms in mitochondrial DNA depletion syndrome

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7 January 2021

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

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7 January 2021

Mitochondrial DNA depletion: prevalence in a pediatric population referred for neurologic evaluation.

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7 January 2021

Mitochondrial DNA depletion syndrome is expressed in amniotic fluid cell cultures.

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7 January 2021

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

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7 January 2021

Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency

1 reference

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7 January 2021

Mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900021-1

7 January 2021

The augmenter of liver regeneration induces mitochondrial gene expression in rat liver and enhances oxidative phosphorylation capacity of liver mitochondria

1 reference

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7 January 2021

10.1016/S0168-8278(02)00021-1

Identifiers

DOI

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10 April 2018

1 reference

10 April 2018