Tyrosinaemia type I: considerations of treatment strategy and experiences with risk assessment, diet and transplantation

Journal of Inherited Metabolic Disease

Volumn 18, Issue 2, 1995, Pages 111-114

  van Spronsen, F J ^a   Smit, G P A ^a   Wijburg, F A ^a   Thomasse, Y ^a   Visser, G ^a   Heymans, H S A ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXANE DERIVATIVE; NITISINONE; UNCLASSIFIED DRUG;

ADOLESCENT; CHILD; CONFERENCE PAPER; CONTROLLED STUDY; DIET THERAPY; DISEASE CLASSIFICATION; DISEASE COURSE; GENETIC HETEROGENEITY; HUMAN; INFANT; LIVER TRANSPLANTATION; MAJOR CLINICAL STUDY; NEWBORN; RISK ASSESSMENT; TREATMENT PLANNING; TYROSINEMIA;

AMINO ACID METABOLISM, INBORN ERRORS; CHILD, PRESCHOOL; GRAFT REJECTION; HUMAN; INFANT; INFANT, NEWBORN; LIVER TRANSPLANTATION; RISK ASSESSMENT; SURVIVAL RATE; TREATMENT OUTCOME; TYROSINE;

EID: 0029037373     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/BF00711742     Document Type: Article

References (15)

1. Hereditary tyrosinemia type I (chronic form): pathologic findings in the liver
2. Liver transplantation for hereditary tyrosinemia in the presence of hepatocellular carcinoma
3. The effects of early treatment of hereditary tyrosinemia type I in infancy for orthotopic liver transplantation
4. Early liver transplantation is indicated for tyrosinemia type I
5. Tyrosinemia
6. Treatment of hereditary tyrosinemia type I by inhibition of 4-hydroxyphenyl-pyruvate dioxygenase
7. Liver transplantation for tyrosinemia. A review of 10 cases from the university of Pittsburgh
8. Neurological crises in hereditary tyrosinemia
9. Liver transplantation for hereditary tyrosinemia: early transplantation following the patient's stabilization
10. Pediatric liver transplantation
11. Tyrosinaemia type I: orthotopic liver transplantation as the only definitive answer to a metabolic as well as an oncological problem
12. Indication and timing of liver replacement in inherited metabolic disorders
13. Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatment
14. The occurrence of hepatoma in the chronic form of hereditary tyrosinemia
15. Liver transplantation in tyrosinemia type I: the Groningen experience