BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 8127063)

  • 21. Neonatal screen for hereditary tyrosinaemia type I.
    Holme E; Lindstedt S
    Lancet; 1992 Oct; 340(8823):850. PubMed ID: 1357267
    [No Abstract]   [Full Text] [Related]  

  • 22. Prenatal diagnosis of tyrosinaemia type I by use of stable isotope dilution mass spectrometry.
    Jakobs C; Kvittingen EA; Berger R; Haagen A; Kleijer W; Niermeijer M
    Eur J Pediatr; 1985 Jul; 144(2):209-10. PubMed ID: 4043138
    [No Abstract]   [Full Text] [Related]  

  • 23. Concentrations of succinylacetone after homogentisate and tyrosine loading in healthy individuals with low fumarylacetoacetase activity.
    Kvittingen EA; Leonard JV; Pettit BR; King GS
    Clin Chim Acta; 1985 Nov; 152(3):271-9. PubMed ID: 4064334
    [TBL] [Abstract][Full Text] [Related]  

  • 24. First-trimester prenatal diagnosis of tyrosinemia type I by amniotic fluid succinylacetone determination.
    Jakobs C; Stellaard F; Kvittingen EA; Henderson M; Lilford R
    Prenat Diagn; 1990 Feb; 10(2):133-4. PubMed ID: 2343022
    [No Abstract]   [Full Text] [Related]  

  • 25. Urinary phenylalanine excretion in hyperphenylalaninemic children.
    Güttler F; Rosleff F
    Acta Paediatr Scand; 1973 Jul; 62(4):333-6. PubMed ID: 4729684
    [No Abstract]   [Full Text] [Related]  

  • 26. Tyrosinaemia II.
    Colditz PB; Yu JS; Billson FA; Rogers M; Molloy HF; O'Halloran M; Wilcken B
    Med J Aust; 1984 Aug; 141(4):244-5. PubMed ID: 6482766
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Renal function in tyrosinaemia type I after liver transplantation: a long-term follow-up.
    Pierik LJ; van Spronsen FJ; Bijleveld CM; van Dael CM
    J Inherit Metab Dis; 2005; 28(6):871-6. PubMed ID: 16435179
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Succinylacetone inhibits delta-aminolevulinate dehydratase and potentiates the drug and steroid induction of delta-aminolevulinate synthase in liver.
    Sassa S; Kappas A
    Trans Assoc Am Physicians; 1982; 95():42-52. PubMed ID: 7182986
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Richner-Hanhart syndrome (oculocutaneous tyrosinaemia, tyrosinaemia type II).
    Paige DG; Clayton P; Bowron A; Harper JI
    J R Soc Med; 1992 Dec; 85(12):759-60. PubMed ID: 1362969
    [No Abstract]   [Full Text] [Related]  

  • 30. Increased excretion of coproporphyrin I in a patient with hereditary tyrosinaemia type I: relevant changes with NTBC treatment.
    Depetris-Boldini C; Galetto R; Videla MP; de Kremer Dodelson R
    J Inherit Metab Dis; 1999 May; 22(3):227-30. PubMed ID: 10384374
    [No Abstract]   [Full Text] [Related]  

  • 31. A case of tyrosinaemia type I with normal level of succinylacetone in the amniotic fluid.
    Grenier A; Cederbaum S; Laberge C; Gagné R; Jakobs C; Tanguay RM
    Prenat Diagn; 1996 Mar; 16(3):239-42. PubMed ID: 8710777
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemia.
    Grenier A; Lescault A; Laberge C; Gagné R; Mamer O
    Clin Chim Acta; 1982 Aug; 123(1-2):93-9. PubMed ID: 7116642
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Two siblings with tyrosinaemia type 2.
    Aydin OF; Zorlu P; Kunak B; Tezic T; Eken A
    Eur J Pediatr; 2003 Feb; 162(2):81-3. PubMed ID: 12548382
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Tyrosinemia].
    Salo MK
    Duodecim; 1992; 108(9):841-3. PubMed ID: 1366298
    [No Abstract]   [Full Text] [Related]  

  • 35. Familial tyrosinaemia with eye and skin lesions. Presentation of two cases.
    Bardelli AM; Borgogni P; Farnetani MA; Fois A; Frezzotti R; Mattei R; Molinelli M; Sargentini I
    Ophthalmologica; 1977; 175(1):5-9. PubMed ID: 20595
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis of hereditary tyrosinaemia: measurement of succinylacetone in amniotic fluid.
    Gagné R; Lescault A; Grenier A; Laberge C; Mélançon SB; Dallaire L
    Prenat Diagn; 1982 Jul; 2(3):185-8. PubMed ID: 7145846
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Liver transplantation in two children with tyrosinaemia type I: biochemical aspects.
    Riudor E; Ribes A; Lloret J; Friden J; Holme E; Jakobs C; Martinez Ibanez V
    J Inherit Metab Dis; 1991; 14(3):281-4. PubMed ID: 1770775
    [No Abstract]   [Full Text] [Related]  

  • 38. Richner-Hanhart syndrome (tyrosinaemia-II) (report of four cases without ocular involvement).
    Rehák A; Selim MM; Yadav G
    Br J Dermatol; 1981 Apr; 104(4):469-75. PubMed ID: 6453606
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hereditary tyrosinemia of chronic course without rickets and renal tubular dysfunction.
    Søvik O; Kvittingen EA; Steen-Johnsen J; Halvorsen S
    Acta Paediatr Scand; 1990 Nov; 79(11):1063-8. PubMed ID: 2267924
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Tyrosinemia].
    Saelzer E; Norero C; Young T
    Rev Chil Pediatr; 1980; 51(6):450-3. PubMed ID: 7221079
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.