Mitochondrial liver diseases;Pathologies hépatiques mitochondriales

Gastroenterologie Clinique et Biologique

Volumn 25, Issue 4 SUPPL., 2001, Pages

  Larrey, D ^a  

^a HÔPITAL SAINT ELOI   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AGING; ALCOHOL LIVER DISEASE; CONFERENCE PAPER; CYTOPATHOLOGY; DISEASE ASSOCIATION; FATTY ACID OXIDATION; FATTY LIVER; HEPATITIS; HUMAN; LIVER DISEASE; LIVER INJURY; MITOCHONDRION; MORPHOLOGY; OXIDATIVE PHOSPHORYLATION; PREGNANCY; RESPIRATORY CHAIN; REYE SYNDROME; STEATOSIS;

DNA, MITOCHONDRIAL; HUMANS; LIVER DISEASES; METABOLISM, INBORN ERRORS; MITOCHONDRIA, LIVER; MUTATION;

EID: 0034924262     PISSN: 03998320     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (22)

1. Drug-induced liver injury
2. Drug-induced steatosis and steatohepatitis
3. Rôle de mitochondries dans l'hépatotoxicité des médicaments
4. Vieillissement, alcool et mitochondries
5. Microvesicular steatosis and steatohepatitis: Role of mitochondrial dysfunction and lipid peroxidation
6. Uncoupling of rat and human mitochondria: A possible explanation for tacrine-induced liver dysfunction
7. Long PCR analysis of human gamete mtDNA suggests defective mitochondrial maintenance in spermatozoa and supports the bottleneck theory for oocytes
8. Mitochondrial DNA mutations and pathogenesis
9. Epidemiology of the A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokeide episodes: Prevalence of the mutation in an adult population
10. Liver failure associated with mitochondrial DNA depletion
11. Fatal neonatal liver failure and mitochondrial cytopathy (oxidative phosphorylation deficiency): A light and electron microscopy study of the liver
12. Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria
13. Three RFLPs defining a haplotype associated with the common mutation in human medium chain acyl-CoA dehydrogenase (MCAD) deficiency occur in Alu repeats
14. Ammonium inhibition of fatty acide oxidation in rat liver mitochondria. A possible cause of fatty liver in Reye's syndrome and urea cycle defects
15. Mitochondrial toxicity of antiviral drugs
16. La stéatose aiguë gravidique: Une maladie aisément curable
17. Assessment of the prevalence of genetic metabolic defects in acute fatty liver of pregnancy
18. Impaired mitochondrial function in microvesicular steatosis. Effects of drugs, ethanol, hormones and cytokines
19. Non-alcoholic steatohepatitis
20. Non-alcoholic steatohepatitis: Another disease of affluence