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 *

116 related articles for article (PubMed ID: 5428587)

  • 1. [New data on pathologic enzymology].
    Dreyfus JC; Schapira F; Kaplan JC; Nordmann Y; Allard D
    Ann Med Interne (Paris); 1970; 121(6):625-8. PubMed ID: 5428587
    [No Abstract]   [Full Text] [Related]  

  • 2. [Our experience of 2 years oferythrocyte enzymology in pediatrics. Apropos of 250 cases].
    Cotte J; Kissin C; Mathieu M; Cuivré M; Freycon F
    Ann Biol Clin (Paris); 1967; 25(10):1129-54. PubMed ID: 4967311
    [No Abstract]   [Full Text] [Related]  

  • 3. Detection of inborn errors of metabolism in 1,117 patients studied because of suspected inherited disease.
    Vaca G; Hernández A; Ibarra B; Velázquez A; Olivares N; Sanchez-Corona J; Medina C; Cantú JM
    Arch Invest Med (Mex); 1981; 12(3):341-8. PubMed ID: 7294941
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Intra-erythrocyte enzyme activities in normal and pathological states].
    Vovan L; Orsini A
    Poumon Coeur; 1971; 27(7):673-81. PubMed ID: 5144943
    [No Abstract]   [Full Text] [Related]  

  • 5. The critically ill child: acute metabolic disease in infancy and early childhood.
    O'Brien D; Goodman SI
    Pediatrics; 1970 Oct; 46(4):620-6. PubMed ID: 5503697
    [No Abstract]   [Full Text] [Related]  

  • 6. [Advances and significance of genetics in pediatrics. Hereditary enzyme defects].
    Prader A
    Monatsschr Kinderheilkd (1902); 1966 Apr; 114(4):188-93. PubMed ID: 5985791
    [No Abstract]   [Full Text] [Related]  

  • 7. [Early diagnosis of enzymatic disorders in protein and carbohydrate metabolism].
    Otter G
    Offentl Gesundheitswes; 1970 Jan; 32(1):11-7. PubMed ID: 4245079
    [No Abstract]   [Full Text] [Related]  

  • 8. On the screening for inborn errors of galactose metabolism.
    Vaca G; Sànchez-Corona J; Olivares N; Medina C; Ibarra B; Cantú JM
    Ann Genet; 1983; 26(3):191-2. PubMed ID: 6606384
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Genetic heterogeneity of hereditary enzymopathies].
    Krasnopol'skaia KD; Bochkov NP
    Vestn Akad Med Nauk SSSR; 1982; (9):56-64. PubMed ID: 7148122
    [No Abstract]   [Full Text] [Related]  

  • 10. [Importance of the study of glucose-6-phosphate dehydrogenase in clinical medicine].
    Seringe P; Kaplan JC; Rosa J; Hoeffel JC; Bertrand C
    Recenti Prog Med; 1968 Oct; 45(4):363-86. PubMed ID: 5755669
    [No Abstract]   [Full Text] [Related]  

  • 11. [Double erythrocyte enzymopathy. Acquired pyruvate kinase and inherited glucose-6-phosphate dehydrogenase deficiencies].
    Herbeuval R; Vigneron C; Aymard JP; Lederlin P; Witz F; Guerci O; Thibaut G
    Nouv Rev Fr Hematol Blood Cells; 1977; 18(1):232-4. PubMed ID: 896451
    [No Abstract]   [Full Text] [Related]  

  • 12. Inborn errors of metabolism. Variability within single diseases.
    Danks DM
    Clin Pediatr (Phila); 1971 Jan; 10(1):1-3. PubMed ID: 5545904
    [No Abstract]   [Full Text] [Related]  

  • 13. Enzyme defects.
    Kirkman HN
    Prog Med Genet; 1972; 8():125-68. PubMed ID: 4551876
    [No Abstract]   [Full Text] [Related]  

  • 14. Serum lysosomal enzyme abnormalities in galactosaemia.
    Jaeken J; Kint J; Spaapen L
    Lancet; 1992 Dec; 340(8833):1472-3. PubMed ID: 1360589
    [No Abstract]   [Full Text] [Related]  

  • 15. Lichen planus; an inborn error of metabolism.
    Cotton DW; Van den Hurk JJ; Van der Staak WB
    Br J Dermatol; 1972 Oct; 87(4):341-6. PubMed ID: 4404021
    [No Abstract]   [Full Text] [Related]  

  • 16. Genetic aspects of enzymopathy.
    Swarup-Mitra S
    Bull Calcutta Sch Trop Med; 1970 Jul; 18(3):88-90. PubMed ID: 5525729
    [No Abstract]   [Full Text] [Related]  

  • 17. [Incidence of erythrocyte deficiency of glucose-6-phosphate dehydrogenase and its relations to jaundice].
    De Virgiliis S; Falorni A; Cao A; Angioni G
    Minerva Ginecol; 1968 Nov; 20(22):1778. PubMed ID: 5751797
    [No Abstract]   [Full Text] [Related]  

  • 18. [Enzyme defects as molecular diseases].
    Aebi H
    Verh Dtsch Ges Inn Med; 1972; 78():304-13. PubMed ID: 4665667
    [No Abstract]   [Full Text] [Related]  

  • 19. Adverse effects of antidepressant drugs.
    Med Lett Drugs Ther; 1975 Jan; 17(1):3-4. PubMed ID: 1109185
    [No Abstract]   [Full Text] [Related]  

  • 20. Metabolic disease of the neonate and young infant.
    Seashore MR; Rinaldo P
    Semin Perinatol; 1993 Oct; 17(5):318-29. PubMed ID: 8290974
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.