Mitochondrial hepatopathies

This publication has 23 references indexed in Scilit:

• Clinical, biochemical and morphological features of hepatocerebral syndrome with mitochondrial DNA depletion due to deoxyguanosine kinase deficiency
  Journal of Hepatology, 2005
• Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase- A
  Brain, 2005
• A Case of Sporadic Infantile Histiocytoid Cardiomyopathy Caused by the A8344G (MERRF) Mitochondrial DNA Mutation
  Pediatric Cardiology, 2004
• POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion
  Annals of Neurology, 2004
• Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene
  Annals of Neurology, 2003
• A Mutation in Mitochondrial DNA-Encoded Cytochrome c Oxidase II Gene in a Child With Alpers-Huttenlocher-Like Disease
  Pediatrics, 2003
• Familial childhood onset neuropathy and cirrhosis with the 4977bp mitochondrial DNA deletion
  American Journal of Medical Genetics, 2002
• A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure
  Nature Genetics, 2001
• Mitochondrial respiratory chain disorders and the liver
  Liver International, 1999
• Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylation
  The Journal of Pediatrics, 1997