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Journal Abstract Search

126 related items for PubMed ID: 5444922

  • 21. Enzyme transplants.
    Lancet; 1972 Dec 09; 2(7789):1235-6. PubMed ID: 4117717
    [No Abstract] [Full Text] [Related]

  • 22. Correction of enzymatic deficiencies by renal transplantation: Fabry's disease.
    Desnick RJ, Simmons RL, Allen KY, Woods JE, Anderson CF, Najarian JS, Krivit W.
    Surgery; 1972 Aug 09; 72(2):203-11. PubMed ID: 4559379
    [No Abstract] [Full Text] [Related]

  • 23. Treatment of Fabry's disease: correction of the enzymatic deficiency by renal transplantation.
    Desnick RJ, Allen KY, Simmons RL, Najarian JS, Krivit W.
    J Lab Clin Med; 1971 Dec 09; 78(6):989-90. PubMed ID: 4943510
    [No Abstract] [Full Text] [Related]

  • 24. [Absent renal ceramide-trihexosidase activity in Fabry's disease].
    Dubach UC, Enderlin F, Mannhart M.
    Ger Med Mon; 1969 Jan 09; 14(1):34-5. PubMed ID: 5352743
    [No Abstract] [Full Text] [Related]

  • 25. Enzymes in amniotic fluid.
    Watkins BF, Bermes EW.
    Ann Clin Lab Sci; 1977 Jan 09; 7(3):231-40. PubMed ID: 193424
    [Abstract] [Full Text] [Related]

  • 26. [Enzyme defects in lipid metabolism].
    Braunsteiner H, Sailer S, Sandhofer F.
    Wien Klin Wochenschr; 1970 Oct 18; 82(42):724-7. PubMed ID: 4097155
    [No Abstract] [Full Text] [Related]

  • 27.
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  • 28. The prenatal diagnosis of inborn errors of metabolism.
    Milunsky A, Littlefield JW.
    Annu Rev Med; 1972 Oct 18; 23():57-76. PubMed ID: 4264784
    [No Abstract] [Full Text] [Related]

  • 29.
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  • 30. [Enzyme defects of fat metabolism].
    Sailer S, Sandhofer F.
    Wien Klin Wochenschr; 1971 Sep 03; 83(35):623-4. PubMed ID: 4109072
    [No Abstract] [Full Text] [Related]

  • 31. Identification of a possible subunit of hexosaminidase A and B.
    Robinson D, Carrol M, Stirling JL.
    Nature; 1973 Jun 15; 243(5407):415-6. PubMed ID: 4743635
    [No Abstract] [Full Text] [Related]

  • 32.
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  • 33. [Histological and histochemical study of a case of angiokeratoma corporis diffusum: Fabry's disease].
    Papilian VV, Grun I.
    Neurol Psihiatr Neurochir; 1970 Jun 15; 15(5):401-9. PubMed ID: 5492050
    [No Abstract] [Full Text] [Related]

  • 34. Gm-gangliosidosis type I: in utero detection and fetal manifestations.
    Kaback MM, Sloan HR, Sonneborn M, Herndon RM, Percy AK.
    J Pediatr; 1973 Jun 15; 82(6):1037-41. PubMed ID: 4702895
    [No Abstract] [Full Text] [Related]

  • 35.
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  • 36. Enzyme replacement therapy by renal allotransplantation in Fabry's disease.
    Clarke JT, Guttmann RD, Wolfe LS, Beaudoin JG, Morehouse DD.
    N Engl J Med; 1972 Dec 14; 287(24):1215-8. PubMed ID: 4563677
    [No Abstract] [Full Text] [Related]

  • 37. Beta-galactosidase in tissue culture derived from human skin and bone marrow. Enzyme defect in GM1 gangliosidosis.
    Sloan HR, Uhlendorf BW, Jacobson CB, Fredrickson DS.
    Pediatr Res; 1969 Nov 14; 3(6):532-7. PubMed ID: 5361691
    [No Abstract] [Full Text] [Related]

  • 38. Prenatal diagnosis of Tay-Sachs disease.
    Schneck L, Valenti C, Amsterdam D, Friedland J, Adachi M, Volk BW.
    Lancet; 1970 Mar 21; 1(7647):582-4. PubMed ID: 4190540
    [No Abstract] [Full Text] [Related]

  • 39. -L-fucosidase and other glycosidases in human placenta, foetus liver and amniotic fluid at various stages of gestation.
    Wiederschain GY, Rosenfeld EL, Brusilovsky AI, Kolibaba LG.
    Clin Chim Acta; 1971 Nov 21; 35(1):99-107. PubMed ID: 5127012
    [No Abstract] [Full Text] [Related]

  • 40. [Fabry's disease].
    Wolfe LS, Mossard JM, Jossot G.
    Presse Med (1893); 1970 Nov 07; 78(47):2051-2. PubMed ID: 5483194
    [No Abstract] [Full Text] [Related]

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