BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 4213051)

  • 1. Editorial: Therapy in genetic disease.
    Erbe RW
    N Engl J Med; 1974 Nov; 291(19):1028-9. PubMed ID: 4213051
    [No Abstract]   [Full Text] [Related]  

  • 2. Enzyme replacement therapy in Gaucher's and Fabry's disease.
    Pentchev PG
    Ann Clin Lab Sci; 1977; 7(3):251-3. PubMed ID: 404951
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An appraisal of human trials in enzyme replacement therapy of genetic diseases.
    Tager JM; Hamers MN; Schram AW; Van den Bergh FA; Rietra PJ; Loonen C; Koster JF; Slee R
    Birth Defects Orig Artic Ser; 1980; 16(1):343-59. PubMed ID: 6778527
    [No Abstract]   [Full Text] [Related]  

  • 4. Replacement therapy for inherited enzyme deficiency. Use of purified glucocerebrosidase in Gaucher's disease.
    Brady RO; Pentchev PG; Gal AE; Hibbert SR; Dekaban AS
    N Engl J Med; 1974 Nov; 291(19):989-93. PubMed ID: 4415565
    [No Abstract]   [Full Text] [Related]  

  • 5. Further developments in studies in sphingolipidoses: "missing enzymes".
    Brady RO
    Riv Patol Nerv Ment; 1970 Oct; 91(5):263-73. PubMed ID: 5525771
    [No Abstract]   [Full Text] [Related]  

  • 6. The lipid storage diseases: new concepts and control.
    Brady RO
    Ann Intern Med; 1975 Feb; 82(2):257-61. PubMed ID: 163609
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An enzymological approach to the lipidoses.
    Tallman JF; Pentchev PG; Brady RO
    Enzyme; 1974; 18(1):136-49. PubMed ID: 4211795
    [No Abstract]   [Full Text] [Related]  

  • 8. Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's disease.
    Brady RO; Tallman JF; Johnson WG; Gal AE; Leahy WR; Quirk JM; Dekaban AS
    N Engl J Med; 1973 Jul; 289(1):9-14. PubMed ID: 4196713
    [No Abstract]   [Full Text] [Related]  

  • 9. Genetic disorders of lysosomes.
    Hirschhorn R; Weissmann G
    Prog Med Genet; 1976; 1():49-101. PubMed ID: 180565
    [No Abstract]   [Full Text] [Related]  

  • 10. [Sphingolipidoses. Biochemistry and enzymatic mechanisms].
    Gajdos A
    Nouv Presse Med; 1972 Jun; 1(26):1789-92. PubMed ID: 5054020
    [No Abstract]   [Full Text] [Related]  

  • 11. [Recent acquisitions in sphingolipidosis].
    Durand P
    Minerva Pediatr; 1970 Jun; 22(24):1233-7. PubMed ID: 5515760
    [No Abstract]   [Full Text] [Related]  

  • 12. Repacement therapy in Gaucher disease.
    Beutler E; Dale GL; Kuhl W
    Birth Defects Orig Artic Ser; 1980; 16(1):369-81. PubMed ID: 6778528
    [No Abstract]   [Full Text] [Related]  

  • 13. Quantity and fatty acyl composition of the glycosphingolipids of Gaucher spleen.
    Kuske TT; Rosenberg A
    J Lab Clin Med; 1972 Oct; 80(4):523-9. PubMed ID: 4342231
    [No Abstract]   [Full Text] [Related]  

  • 14. [Biochemical aspects of sphingolipidosis].
    Douste-Blazy L; Thouvenot JP
    Ann Biol Clin (Paris); 1972; 30(6):623-35. PubMed ID: 4569435
    [No Abstract]   [Full Text] [Related]  

  • 15. Investigations in enzyme replacement therapy in lipid storage diseases.
    Brady RO; Pentchev PG; Gal AG
    Fed Proc; 1975 Apr; 34(5):1310-5. PubMed ID: 804420
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chemical chaperones--a new concept in drug research.
    Kolter T; Wendeler M
    Chembiochem; 2003 Apr; 4(4):260-4. PubMed ID: 12672104
    [No Abstract]   [Full Text] [Related]  

  • 17. Enzyme therapy for inborn errors of metabolism.
    Desnick RJ; Bernlohr RW; Krivit W
    Postgrad Med; 1973 Jan; 53(1):214-6. PubMed ID: 4508960
    [No Abstract]   [Full Text] [Related]  

  • 18. Renal transplantation in Type II Gaucher disease.
    Desnick SJ; Desnick RJ; Brady RO; Pentchev PG; Simmons RL; Najarian JS; Swaiman K; Sharp HL; Krivit W
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):109-19. PubMed ID: 4611522
    [No Abstract]   [Full Text] [Related]  

  • 19. Diagnostic and therapeutic applications of sphingolipid hydrolyzing enzymes.
    Brady RO
    Curr Top Cell Regul; 1985; 26():39-50. PubMed ID: 3935381
    [No Abstract]   [Full Text] [Related]  

  • 20. Enzyme replacement in Fabry disease: treatment of cultured skin fibroblasts with a purified alpha-galactosidase from ficin.
    Dawson G; Matalon R; Li YT
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):97-101. PubMed ID: 4215480
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.