Mitochondrial Hepatopathy

A liver disorder caused by primary or secondary defects in the function of the mitochondria in the hepatocytes.
National Institutes of Health

Topic mentions per year

Topic mentions per year

2003-2017
02420032017

Papers overview

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2017
2017
The French-Canadian variant of Leigh Syndrome (LSFC) is an autosomal recessive oxidative phosphorylation (OXPHOS) disorder caused… (More)
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2017
2017
Mitochondrial disorders are among the most prevalent inborn errors of metabolism but largely lack treatments and have poor… (More)
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2013
2013
3-Methylglutaconic aciduria (3-MGCA) type IV is defined as a heterogeneous group of inborn errors featuring in common 3-MGCA and… (More)
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2012
2012
BACKGROUND & AIMS Liver is a target organ in many mitochondrial disorders, especially if the complex III assembly factor BCS1L is… (More)
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Review
2012
Review
2012
Cholestatic liver diseases are characterized by blockade of bile flow from the liver to the intestine, and accumulation of… (More)
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2011
2011
UNLABELLED Mitochondrial dysfunction is an important cause for neonatal liver disease. Disruption of genes encoding oxidative… (More)
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2011
2011
Chronic cholestasis is characterized by mitochondrial dysfunction, associated with loss of mitochondrial membrane potential… (More)
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2011
2011
CONTEXT AND OBJECTIVE In children, hepatic steatosis may be related to inborn errors of metabolism (IEMs) or to non-alcoholic… (More)
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Review
2011
Review
2011
Mitochondrial disorders recognized in the neonatal period usually present as a metabolic crisis combined with one or several… (More)
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2003
2003
OBJECTIVES To document 2 apparently incongruous clinical disorders occurring in the same infant: congenital myopathy with… (More)
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