HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase.

AuthorsM A Vilaseca, P Briones, A Ribes, E Carreras, A Llácer, J Querol
JournalJournal of inherited metabolic disease (J Inherit Metab Dis) Vol. 14 Issue 3 Pg. 285-8 ( 1991) ISSN: 0141-8955 [Print] United States
PMID1663190 (Publication Type: Journal Article)
Chemical References
  • Amino Acids
  • Isothiocyanates
  • Thiocyanates
  • phenylisothiocyanate
  • Succinate Cytochrome c Oxidoreductase
Topics
  • Acidosis, Lactic (blood, complications, enzymology)
  • Amino Acids (blood)
  • Fanconi Syndrome (complications, enzymology, metabolism)
  • Female
  • Gas Chromatography-Mass Spectrometry
  • Humans
  • Infant
  • Isothiocyanates
  • Liver Diseases (complications, enzymology, metabolism)
  • Male
  • Succinate Cytochrome c Oxidoreductase (deficiency)
  • Thiocyanates

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: