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Page 1
alpha-Galactosidase A deficient mice: a model of Fabry disease.
Ohshima T, Murray GJ, Swaim WD, Longenecker G, Quirk JM, Cardarelli CO, Sugimoto Y, Pastan I, Gottesman MM, Brady RO, Kulkarni AB. Ohshima T, et al. Among authors: quirk jm. Proc Natl Acad Sci U S A. 1997 Mar 18;94(6):2540-4. doi: 10.1073/pnas.94.6.2540. Proc Natl Acad Sci U S A. 1997. PMID: 9122231 Free PMC article.
Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease.
Schiffmann R, Murray GJ, Treco D, Daniel P, Sellos-Moura M, Myers M, Quirk JM, Zirzow GC, Borowski M, Loveday K, Anderson T, Gillespie F, Oliver KL, Jeffries NO, Doo E, Liang TJ, Kreps C, Gunter K, Frei K, Crutchfield K, Selden RF, Brady RO. Schiffmann R, et al. Among authors: quirk jm. Proc Natl Acad Sci U S A. 2000 Jan 4;97(1):365-70. doi: 10.1073/pnas.97.1.365. Proc Natl Acad Sci U S A. 2000. PMID: 10618424 Free PMC article. Clinical Trial.
Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course.
Branton MH, Schiffmann R, Sabnis SG, Murray GJ, Quirk JM, Altarescu G, Goldfarb L, Brady RO, Balow JE, Austin Iii HA, Kopp JB. Branton MH, et al. Among authors: quirk jm. Medicine (Baltimore). 2002 Mar;81(2):122-38. doi: 10.1097/00005792-200203000-00003. Medicine (Baltimore). 2002. PMID: 11889412 Free article. No abstract available.
35 results