These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 8929295)

  • 1. Imaging features of type 1 hereditary tyrosinemia: a review of 30 patients.
    Dubois J; Garel L; Patriquin H; Paradis K; Forget S; Filiatrault D; Grignon A; Russo P; St-Vil D
    Pediatr Radiol; 1996 Dec; 26(12):845-51. PubMed ID: 8929295
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The kidney in children with tyrosinemia: sonographic, CT and biochemical findings.
    Forget S; Patriquin HB; Dubois J; Lafortune M; Merouani A; Paradis K; Russo P
    Pediatr Radiol; 1999 Feb; 29(2):104-8. PubMed ID: 9933329
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary tyrosinemia type I--an overview.
    Kvittingen EA
    Scand J Clin Lab Invest Suppl; 1986; 184():27-34. PubMed ID: 3296130
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Liver transplantation for hereditary tyrosinemia: the Quebec experience.
    Paradis K; Weber A; Seidman EG; Larochelle J; Garel L; Lenaerts C; Roy CC
    Am J Hum Genet; 1990 Aug; 47(2):338-42. PubMed ID: 2378360
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pediatric case of the day. Hepatorenal tyrosinemia (tyrosinemia type I).
    Gallant JM; Barnewolt CE; Buonomo C
    Radiographics; 1996 Sep; 16(5):1221-4. PubMed ID: 8888402
    [No Abstract]   [Full Text] [Related]  

  • 6. Tyrosinemia: the Quebec experience.
    Paradis K
    Clin Invest Med; 1996 Oct; 19(5):311-6. PubMed ID: 8889268
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Visceral pathology of hereditary tyrosinemia type I.
    Russo P; O'Regan S
    Am J Hum Genet; 1990 Aug; 47(2):317-24. PubMed ID: 2378357
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hepatic imaging with computed tomography of chronic tyrosinaemia type 1.
    Macvicar D; Dicks-Mireaux C; Leonard JV; Wight DG
    Br J Radiol; 1990 Aug; 63(752):605-8. PubMed ID: 2400875
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tyrosinemia type 1 should be suspected in infants with severe coagulopathy even in the absence of other signs of liver failure.
    Croffie JM; Gupta SK; Chong SK; Fitzgerald JF
    Pediatrics; 1999 Mar; 103(3):675-8. PubMed ID: 10049978
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The effects of early treatment of hereditary tyrosinemia type I in infancy by orthotopic liver transplantation.
    Flye MW; Riely CA; Hainline BE; Sassa S; Gusberg RJ; Blakemore KJ; Barwick KW; Horwich AL
    Transplantation; 1990 May; 49(5):916-21. PubMed ID: 2336709
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pathological case of the month. Hereditary tyrosinemia type I.
    Barness L; Gilbert-Barness E
    Am J Dis Child; 1992 Jun; 146(6):769-70. PubMed ID: 1595638
    [No Abstract]   [Full Text] [Related]  

  • 12. [Sepsis, as the presenting form of hereditary tyrosinemia type I].
    Iglesias Niubo J; Riudor Taravilla E; Goma Brufau AR; Civit Colas MA; Suñé Gracia JM; Bertrán Sanges JM; Gallart Catalá A
    An Esp Pediatr; 1988 Sep; 29(3):235-8. PubMed ID: 3057981
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nephropathy of tyrosinemia and its long-term outlook.
    Paradis K; D'Angata ID
    J Pediatr Gastroenterol Nutr; 1997 Jan; 24(1):113-4. PubMed ID: 9093996
    [No Abstract]   [Full Text] [Related]  

  • 14. [Surgical and metabolic aspects of liver transplantation for tyrosinemia].
    Bruneau N; St-Vil D; Luks FI; LaBerge JM; Bensoussan AL; Blanchard H
    Ann Chir; 1993; 47(9):803-9. PubMed ID: 8141543
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The nephropathy of type I tyrosinemia after liver transplantation.
    Laine J; Salo MK; Krogerus L; Kärkkäinen J; Wahlroos O; Holmberg C
    Pediatr Res; 1995 May; 37(5):640-5. PubMed ID: 7603784
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Surgical and metabolic aspects of liver transplantation for tyrosinemia.
    Luks FI; St-Vil D; Hancock BJ; Laberge JM; Bensoussan AL; Russo P; Mitchell G; Lambert M; Blanchard H
    Transplantation; 1993 Dec; 56(6):1376-80. PubMed ID: 8279006
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neurologic crises in hereditary tyrosinemia.
    Mitchell G; Larochelle J; Lambert M; Michaud J; Grenier A; Ogier H; Gauthier M; Lacroix J; Vanasse M; Larbrisseau A
    N Engl J Med; 1990 Feb; 322(7):432-7. PubMed ID: 2153931
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rapid improvement in the renal tubular dysfunction associated with tyrosinemia following hepatic replacement.
    Shoemaker LR; Strife CF; Balistreri WF; Ryckman FC
    Pediatrics; 1992 Feb; 89(2):251-5. PubMed ID: 1734392
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Special imaging casebook. Hereditary tyrosinemia, acute type I.
    Herman TE; McAlister WH; Siegel MJ
    J Perinatol; 1997; 17(1):87-90. PubMed ID: 9069074
    [No Abstract]   [Full Text] [Related]  

  • 20. A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type I.
    Grompe M; St-Louis M; Demers SI; al-Dhalimy M; Leclerc B; Tanguay RM
    N Engl J Med; 1994 Aug; 331(6):353-7. PubMed ID: 8028615
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.