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4. Anomeric structure of ceramide digalactoside isolated from the kidney of a patient with Fabry's disease. Li YT; Li SC; Dawson G Biochim Biophys Acta; 1972 Jan; 260(1):88-92. PubMed ID: 5012456 [No Abstract] [Full Text] [Related]
8. Absence of cross-reactive antigen in Fabry's disease. Beutler E; Kuhl W N Engl J Med; 1973 Sep; 289(13):694-5. PubMed ID: 4199465 [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; 64():36-8. PubMed ID: 4569857 [No Abstract] [Full Text] [Related]
10. Evidence for a terminal -D-galactopyranosyl residue in galactosylgalactosylglucosylceramide from human kidney. Clarke JT; Wolfe LS; Perlin AS J Biol Chem; 1971 Sep; 246(18):5563-9. PubMed ID: 5096082 [No Abstract] [Full Text] [Related]
11. 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; 7(8):684-90. PubMed ID: 4732107 [No Abstract] [Full Text] [Related]
12. Reversal of an inborn sphingolipidosis (Fabry's disease) by kidney transplantation. Philippart M; Franklin SS; Gordon A Ann Intern Med; 1972 Aug; 77(2):195-200. PubMed ID: 4565790 [No Abstract] [Full Text] [Related]
13. Fabry's disease: differentiation between two forms of -galactosidase by myoinositol. Crawhall JC; Banfalvi M Science; 1972 Aug; 177(4048):527-8. PubMed ID: 5050485 [TBL] [Abstract][Full Text] [Related]
14. The biochemical abnormalities in Fabry's disease. Kint JA; Dacremont G Arch Int Physiol Biochim; 1970 Feb; 78(1):169-71. PubMed ID: 4100872 [No Abstract] [Full Text] [Related]
15. 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; 81(2):157-71. PubMed ID: 4683418 [No Abstract] [Full Text] [Related]
16. Kidney transplantation in Fabry's disease. Philippart M; Franklin SS; Leeber DA; Hull AR; Peters PC N Engl J Med; 1973 Aug; 289(5):270-1. PubMed ID: 4197403 [No Abstract] [Full Text] [Related]
17. [Autopsy case of Fabry's disease]. Yoshitoshi Y; Nagata N; Nakamura K; Nishio I Naika; 1971 May; 27(5):983-7. PubMed ID: 5572502 [No Abstract] [Full Text] [Related]
18. 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]