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2. Diagnosis of glycosphingolipidoses by urinary-sediment analysis. Desnick RJ; Dawson G; Desnick SJ; Sweeley CC; Krivit W N Engl J Med; 1971 Apr; 284(14):739-44. PubMed ID: 5548035 [No Abstract] [Full Text] [Related]
3. Pathologic lysosomes and increased urinary glycosylceramide excretion in Fabry's disease. Studies on a family with evidence of linkage with the sex-linked blood group Xg. Malmqvist E; Ivemark BI; Lindsten J; Maunsbach AB; MÃ¥rtensson E Lab Invest; 1971 Jul; 25(1):1-14. PubMed ID: 4326523 [No Abstract] [Full Text] [Related]
10. 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]
11. Fine structure of the skin in angiokeratoma corporis diffusum (Fabry's disease). van Mullem PJ; Ruiter M J Pathol; 1970 Jul; 101(3):221-6. PubMed ID: 4098426 [No Abstract] [Full Text] [Related]
12. 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]
13. Fabry's disease as an -galactosidosis: evidence for an -configuration in trihexosyl ceramide. Bensaude I; Callahan J; Philippart M Biochem Biophys Res Commun; 1971 May; 43(4):913-8. PubMed ID: 5563756 [No Abstract] [Full Text] [Related]
16. 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; 72(2):203-11. PubMed ID: 4559379 [No Abstract] [Full Text] [Related]
17. 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]