Brady RO - Search Results

1

Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease.

Barton NW, Brady RO, Dambrosia JM, Di Bisceglie AM, Doppelt SH, Hill SC, Mankin HJ, Murray GJ, Parker RI, Argoff CE, et al. Barton NW, et al. Among authors: brady ro. N Engl J Med. 1991 May 23;324(21):1464-70. doi: 10.1056/NEJM199105233242104. N Engl J Med. 1991. PMID: 2023606 Free article. Clinical Trial.

2

MRI of multiple platyspondyly in Gaucher disease: response to enzyme replacement therapy.

Hill SC, Parker CC, Brady RO, Barton NW. Hill SC, et al. Among authors: brady ro. J Comput Assist Tomogr. 1993 Sep-Oct;17(5):806-9. doi: 10.1097/00004728-199309000-00026. J Comput Assist Tomogr. 1993. PMID: 8370839

3

Treatment of Gaucher's disease.

Barton NW, Brady RO, Dambrosia JM. Barton NW, et al. Among authors: brady ro. N Engl J Med. 1993 May 27;328(21):1564-5; author reply 1567-8. N Engl J Med. 1993. PMID: 8479496 No abstract available.

4

Analysis of the lipids of normal and Gaucher bone marrow.

Miller SP, Zirzow GC, Doppelt SH, Brady RO, Barton NW. Miller SP, et al. Among authors: brady ro. J Lab Clin Med. 1996 Apr;127(4):353-8. doi: 10.1016/s0022-2143(96)90183-3. J Lab Clin Med. 1996. PMID: 8656038

5

Enzyme replacement and gene therapy for Gaucher's disease.

Brady RO, Barton NW. Brady RO, et al. Lipids. 1996 Mar;31 Suppl:S137-9. doi: 10.1007/BF02637065. Lipids. 1996. PMID: 8729108

6

Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease.

Schiffmann R, Heyes MP, Aerts JM, Dambrosia JM, Patterson MC, DeGraba T, Parker CC, Zirzow GC, Oliver K, Tedeschi G, Brady RO, Barton NW. Schiffmann R, et al. Among authors: brady ro. Ann Neurol. 1997 Oct;42(4):613-21. doi: 10.1002/ana.410420412. Ann Neurol. 1997. PMID: 9382473 Clinical Trial.

7

Management of neutralizing antibody to Ceredase in a patient with type 3 Gaucher disease.

Brady RO, Murray GJ, Oliver KL, Leitman SF, Sneller MC, Fleisher TA, Barton NW. Brady RO, et al. Pediatrics. 1997 Dec;100(6):E11. doi: 10.1542/peds.100.6.e11. Pediatrics. 1997. PMID: 9382912

8

Comparative efficacy of dose regimens in enzyme replacement therapy of type I Gaucher disease.

Altarescu G, Schiffmann R, Parker CC, Moore DF, Kreps C, Brady RO, Barton NW. Altarescu G, et al. Among authors: brady ro. Blood Cells Mol Dis. 2000 Aug;26(4):285-90. doi: 10.1006/bcmd.2000.0310. Blood Cells Mol Dis. 2000. PMID: 11042029 Clinical Trial.

9

The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's disease.

Altarescu G, Hill S, Wiggs E, Jeffries N, Kreps C, Parker CC, Brady RO, Barton NW, Schiffmann R. Altarescu G, et al. Among authors: brady ro. J Pediatr. 2001 Apr;138(4):539-47. doi: 10.1067/mpd.2001.112171. J Pediatr. 2001. PMID: 11295718

10

Gaucher disease: abdominal MR imaging findings in 46 patients.

Hill SC, Damaska BM, Ling A, Patterson K, Di Bisceglie AM, Brady RO, Barton NW. Hill SC, et al. Among authors: brady ro. Radiology. 1992 Aug;184(2):561-6. doi: 10.1148/radiology.184.2.1620865. Radiology. 1992. PMID: 1620865

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