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 *

115 related articles for article (PubMed ID: 4180556)

  • 1. Fructosaemia-"acute-tyrosinosis".
    Lindemann R; Gjessing LR; Merton B; Halvorsen S
    Lancet; 1969 Apr; 1(7600):891. PubMed ID: 4180556
    [No Abstract]   [Full Text] [Related]  

  • 2. Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis".
    Bakker HD; de Bree PK; van Sprang FJ; Wadman SK
    Clin Chim Acta; 1974 Aug; 55(1):41-7. PubMed ID: 4370029
    [No Abstract]   [Full Text] [Related]  

  • 3. [Disorders in the tyrosine metabolism. II. Tyrosinemia - a congenital metabolic disorder].
    Vulović D; Hajduković R; Sindjić M; FilipovićD ; Dozić S
    Srp Arh Celok Lek; 1974 Jan; 102(1):9-20. PubMed ID: 4368107
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. [Hypertyrosinemia with hypermethioninemia in the newborn in a case of fructose intolerance].
    Willems C; Heusden A; Renson P; Legat C; Monard Y; Stainier L
    Helv Paediatr Acta; 1971 Oct; 26(4):467-81. PubMed ID: 5123311
    [No Abstract]   [Full Text] [Related]  

  • 6. Significance of hypermethionaemia in acute tyrosinosis.
    Gaull GE; Rassin DK; Sturman JA
    Lancet; 1968 Jun; 1(7555):1318-9. PubMed ID: 4172182
    [No Abstract]   [Full Text] [Related]  

  • 7. Significance of hypermethionaemia in acute tyrosinosis.
    Scriver CR
    Lancet; 1968 Jun; 1(7555):1319. PubMed ID: 4172183
    [No Abstract]   [Full Text] [Related]  

  • 8. Inborn errors of metabolism: the essentials of clinical diagnosis.
    Roth KS
    Clin Pediatr (Phila); 1991 Mar; 30(3):183-90. PubMed ID: 2009725
    [No Abstract]   [Full Text] [Related]  

  • 9. Abnormal tyrosine metabolism in hereditary fructose intolerance.
    Grant DB; Alexander FW; Seakins JW
    Acta Paediatr Scand; 1970 Jul; 59(4):432-4. PubMed ID: 5447686
    [No Abstract]   [Full Text] [Related]  

  • 10. [Tyrosinosis].
    Halvorsen S
    Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):31-2. PubMed ID: 5398915
    [No Abstract]   [Full Text] [Related]  

  • 11. Inborn errors of organic acid metabolism.
    Green A
    Br J Hosp Med; 1989 May; 41(5):426-30, 432, 434. PubMed ID: 2663104
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neonatal hepatitis in premature infants simulating hereditary tyrosinosis.
    Yu JS; Walker-Smith JA; Burnard ED
    Arch Dis Child; 1971 Jun; 46(247):306-9. PubMed ID: 5090663
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Laboratory expands screening procedures.
    Murphree JT
    J Med Assoc State Ala; 1968 Nov; 38(5):404-5. PubMed ID: 5725300
    [No Abstract]   [Full Text] [Related]  

  • 14. Diagnosis and treatment of tyrosinosis.
    Fairney A; Francis D; Ersser RS; Seakins JW; Cottom D
    Arch Dis Child; 1968 Oct; 43(231):540-7. PubMed ID: 5696464
    [No Abstract]   [Full Text] [Related]  

  • 15. [1H-NMR urinalysis: simultaneous screening of inborn errors of metabolism of amino acid and organic acid disorders].
    Yamamoto H; Yamaguchi S
    Rinsho Byori; 1988 Feb; 36(2):182-90. PubMed ID: 3379790
    [No Abstract]   [Full Text] [Related]  

  • 16. Neurometabolic disorders in infancy, childhood and adolescence.
    Hagberg B
    Acta Neurol Scand; 1967; 43(S31):13-19. PubMed ID: 5583240
    [No Abstract]   [Full Text] [Related]  

  • 17. [Severe metabolic diseases in neonates. Diagnosis and treatment (author's transl)].
    Koepp P; Grüttner R
    Klin Padiatr; 1975 Jan; 187(1):14-9. PubMed ID: 1168276
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Neonatal diagnosis of hereditary metabolic diseases].
    Lambotte C
    Rev Med Liege; 1973 Dec; 28(24):837-51. PubMed ID: 4769974
    [No Abstract]   [Full Text] [Related]  

  • 19. [Tyrosinosis. A difficult diagnosis of late infancy].
    Bertolani MF; Pellegrino AM; Summa C; Scalera E
    Minerva Pediatr; 1990; 42(1-2):1-7. PubMed ID: 2159592
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Dietetics in hereditary enzyme deficiencies].
    Royer P
    Sem Hop; 1970 Feb; 46(10):653-9. PubMed ID: 4314674
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.