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Journal Abstract Search
139 related items for PubMed ID: 5028965
1. Fabry's disease: absence of an -galactosidase isozyme. Wood S, Nadler HL. Am J Hum Genet; 1972 May; 24(3):250-5. PubMed ID: 5028965 [No Abstract] [Full Text] [Related]
2. Fabry's disease: evidence for a physically altered -galactosidase. Ho MW, Beutler S, Tennant L, O'Brien JS. Am J Hum Genet; 1972 May; 24(3):256-66. PubMed ID: 5028966 [No Abstract] [Full Text] [Related]
3. Biochemical and electrophoretic studies of -galactosidase in normal man, in patients with Fabry's disease, and in Equidae. Beutler E, Kuhl W. Am J Hum Genet; 1972 May; 24(3):237-49. PubMed ID: 5028964 [No Abstract] [Full Text] [Related]
4. Fabry's disease: differentiation between two forms of -galactosidase by myoinositol. Crawhall JC, Banfalvi M. Science; 1972 Aug 11; 177(4048):527-8. PubMed ID: 5050485 [Abstract] [Full Text] [Related]
5. Fabry's disease: the search for a regulator gene mutation in man. Sutton HE, Omenn GS. Am J Hum Genet; 1972 May 11; 24(3):343-7. PubMed ID: 5028973 [No Abstract] [Full Text] [Related]
6. Genetic inactivation of the alpha-galactosidase locus in carriers of Fabry's disease. Romeo G, Migeon BR. Science; 1970 Oct 09; 170(3954):180-1. PubMed ID: 5466114 [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 09; 7(8):684-90. PubMed ID: 4732107 [No Abstract] [Full Text] [Related]