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 *

121 related articles for article (PubMed ID: 5694370)

  • 1. Hereditary tyrosinemia.
    JAMA; 1968 Mar; 203(12):1062. PubMed ID: 5694370
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hereditary tyrosinemia. IV. Pathogenesis. New therapeutic perspectives].
    Bélanger L; Larochelle J; Bélanger M; Privé L
    Pediatrie; 1973; 28(1):35-55. PubMed ID: 4715466
    [No Abstract]   [Full Text] [Related]  

  • 3. Biochemical observations on so-called hereditary tyrosinemia.
    Gaull GE; Rassin DK; Solomon GE; Harris RC; Sturman JA
    Pediatr Res; 1970 Jul; 4(4):337-44. PubMed ID: 4393588
    [No Abstract]   [Full Text] [Related]  

  • 4. Hereditary tyrosinemia. 3. On the differential diagnosis and the lack of effect of early dietary treatment.
    Bodegård G; Gentz J; Lindblad B; Lindstedt S; Zetterström R
    Acta Paediatr Scand; 1969 Jan; 58(1):37-48. PubMed ID: 5789740
    [No Abstract]   [Full Text] [Related]  

  • 5. Hereditary tyrosinemia: metabolic studies in a patient with partial p-hydroxyphenylpyruvate hydroxylase activity.
    Jagenburg R; Landblad B; De Maré JM; Rödjer S
    J Pediatr; 1972 Jun; 80(6):994-1004. PubMed ID: 5026040
    [No Abstract]   [Full Text] [Related]  

  • 6. [Dietary management of hereditary tyrosinemia. Apropos of 7 cases].
    Jehan P; Buchman M; Odièvre M
    Ann Pediatr (Paris); 1984 Jan; 31(1):33-40. PubMed ID: 6712098
    [No Abstract]   [Full Text] [Related]  

  • 7. [Juvenile form of tyrosinemia type I].
    Nothjunge J; Rosendahl W
    Klin Padiatr; 1989; 201(6):458-63. PubMed ID: 2601281
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dietary treatment of tyrosinemia type I: importance of methionine restriction.
    Michals K; Matolon R; Wong PW
    J Am Diet Assoc; 1978 Nov; 73(5):507-14. PubMed ID: 701680
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hereditary tyrosinemia and tyrosyluria in a French Canadian geographic isolate.
    Scriver CR; Larochelle J; Silverberg M
    Am J Dis Child; 1967 Jan; 113(1):41-6. PubMed ID: 6016174
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hereditary tyrosinemia and vitamin-dependent rickets in Saguenay. A genetic and demographic approach].
    Bouchard G; Laberge C; Scriver CR
    Union Med Can; 1985 Aug; 114(8):633-6. PubMed ID: 4060342
    [No Abstract]   [Full Text] [Related]  

  • 11. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia.
    Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R
    Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976
    [No Abstract]   [Full Text] [Related]  

  • 12. Hereditary tyrosinemia in the province of Quebec: prevalence at birth and geographic distribution.
    Bergeron P; Laberge C; Grenier A
    Clin Genet; 1974; 5(2):157-62. PubMed ID: 4829425
    [No Abstract]   [Full Text] [Related]  

  • 13. [Hereditary tyrosinemia].
    Halvorsen S
    Ugeskr Laeger; 1979 Sep; 141(37):2540-1. PubMed ID: 483445
    [No Abstract]   [Full Text] [Related]  

  • 14. Recovery after dietary treatment of an infant with features of tyrosinosis.
    Harries JT; Seakins JW; Ersser RS; Lloyd JK
    Arch Dis Child; 1969 Apr; 44(234):258-67. PubMed ID: 5779435
    [No Abstract]   [Full Text] [Related]  

  • 15. Evidence for liver disease preceding amino acid abnormalities in hereditary tyrosinemia.
    Hostetter MK; Levy HL; Winter HS; Knight GJ; Haddow JE
    N Engl J Med; 1983 May; 308(21):1265-7. PubMed ID: 6188953
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A rare cause of neonatal hyperphenylalaninemia: tyrosinemia type I].
    Sarles J; Maurin N; Giraud F
    Pediatrie; 1992; 47(12):809-11. PubMed ID: 1338924
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Chronic hereditary tyrosinemia].
    Morán-Vázquez JO; Sánchez-Corona J; Pérez-Molina J; Viruete-Alcaraz M; Venegas-Mesina R
    Bol Med Hosp Infant Mex; 1987 Sep; 44(9):540-5. PubMed ID: 3663321
    [No Abstract]   [Full Text] [Related]  

  • 18. [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]  

  • 19. The enzymatic deficiency in tyrosinemia.
    Du BN
    Can Med Assoc J; 1967 Oct; 97(18):1076-8. PubMed ID: 6050909
    [No Abstract]   [Full Text] [Related]  

  • 20. Cholestasis and hypermethioninemia during dietary management of hereditary tyrosinemia type 1.
    Ameen VZ; Powell GK; Rassin DK
    J Pediatr; 1986 Jun; 108(6):949-52. PubMed ID: 2872285
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.