Liver failure associated with mitochondrial DNA depletion (Q74497818)

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11 November 2019

title

Liver failure associated with mitochondrial DNA depletion (English)

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11 November 2019

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2

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11 November 2019

Peter Theodore Clayton

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ORCID Public Data File 2021

Anthony H V Schapira

10

object named as

A H Schapira

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4

J M Cooper

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author name string

A A Morris

1

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11 November 2019

J Blake

3

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11 November 2019

B D Lake

5

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11 November 2019

M Malone

6

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11 November 2019

S Love

7

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P T Clayton

8

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J V Leonard

9

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publication date

1 April 1998

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11 November 2019

published in

Journal of Hepatology

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11 November 2019

volume

28

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issue

4

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page(s)

556-563

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describes a project that uses

11 November 2019

1 reference

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980278-X

7 January 2021

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

1 reference

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Deficiency of respiratory chain complex I is a common cause of Leigh disease.

1 reference

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Molecular mechanisms in mitochondrial DNA depletion syndrome

1 reference

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7 January 2021

Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

1 reference

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7 January 2021

A rapid protocol for the purification of mitochondrial DNA suitable for studying restriction fragment length polymorphisms

1 reference

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7 January 2021

Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Changes in the number of mitochondrial genomes during human development

1 reference

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7 January 2021

Mitochondrial gene expression during bovine cardiac growth and development.

1 reference

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7 January 2021

Fatal infantile liver failure associated with mitochondrial DNA depletion

1 reference

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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

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7 January 2021

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

1 reference

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7 January 2021

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980278-X

7 January 2021

Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study

1 reference

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7 January 2021

Early-onset fatal encephalomyopathy associated with severe mtDNA depletion

1 reference

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7 January 2021

Familial cardiomyopathy with cataracts and lactic acidosis: a defect in complex I (NADH-dehydrogenase) of the mitochondria respiratory chain

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980278-X

7 January 2021

Mitochondrial electron transport chain defect presenting as hypoglycemia

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980278-X

7 January 2021

Fatal cytochrome c oxidase-deficient myopathy of infancy associated with mtDNA depletion. Differential involvement of skeletal muscle and cultured fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2898%2980278-X

7 January 2021

10.1016/S0168-8278(98)80278-X

Identifiers

DOI

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11 November 2019

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