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Journal Abstract Search
181 related items for PubMed ID: 4196713
1. 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 05; 289(1):9-14. PubMed ID: 4196713 [No Abstract] [Full Text] [Related]
2. Letter: Enhancement of enzymatic activity in Fabry's disease. Christensen E. N Engl J Med; 1974 Mar 14; 290(11):629-30. PubMed ID: 4204696 [No Abstract] [Full Text] [Related]
3. 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]
7. Correction of the enzymic defect in cultured fibroblasts from patients with Fabry's disease: treatment with purified alpha-galactosidase from ficin. Dawson G, Matalon R, Li YT. Pediatr Res; 1973 Aug 14; 7(8):684-90. PubMed ID: 4732107 [No Abstract] [Full Text] [Related]
8. 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 14; 9(2):97-101. PubMed ID: 4215480 [No Abstract] [Full Text] [Related]
9. Renal transplantation in Fabry's disease. Peters PC, Leeber D, Hull AR, Philippart M. Trans Am Assoc Genitourin Surg; 1972 Mar 14; 64():36-8. PubMed ID: 4569857 [No Abstract] [Full Text] [Related]
10. 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 14; 78(6):989-90. PubMed ID: 4943510 [No Abstract] [Full Text] [Related]
11. 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 14; 72(2):203-11. PubMed ID: 4559379 [No Abstract] [Full Text] [Related]
12. [Fabry-Anderson's disease]. Andratschke C. Fortschr Med; 1975 Dec 04; 93(34):1697-702. PubMed ID: 811519 [Abstract] [Full Text] [Related]
13. Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. Alpha-galactosidase activities in plasma, serum, urine, and leukocytes. Desnick RJ, Allen KY, Desnick SJ, Raman MK, Bernlohr RW, Krivit W. J Lab Clin Med; 1973 Feb 04; 81(2):157-71. PubMed ID: 4683418 [No Abstract] [Full Text] [Related]
14. Reversal of an inborn sphingolipidosis (Fabry's disease) by kidney transplantation. Philippart M, Franklin SS, Gordon A. Ann Intern Med; 1972 Aug 04; 77(2):195-200. PubMed ID: 4565790 [No Abstract] [Full Text] [Related]
15. Absence of cross-reactive antigen in Fabry's disease. Beutler E, Kuhl W. N Engl J Med; 1973 Sep 27; 289(13):694-5. PubMed ID: 4199465 [No Abstract] [Full Text] [Related]