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Page 1
Gaucher disease: Progress and ongoing challenges.
Mistry PK, Lopez G, Schiffmann R, Barton NW, Weinreb NJ, Sidransky E. Mistry PK, et al. Among authors: barton nw. Mol Genet Metab. 2017 Jan-Feb;120(1-2):8-21. doi: 10.1016/j.ymgme.2016.11.006. Epub 2016 Nov 17. Mol Genet Metab. 2017. PMID: 27916601 Free PMC article. Review.
Roscoe Owen Brady, MD: Remembrances of co-investigators and colleagues.
Desnick RJ, Barton NW, Furbish S, Grabowski GA, Karlsson S, Kolodny EH, Medin JA, Murray GJ, Mistry PK, Patterson MC, Schiffmann R, Weinreb NJ. Desnick RJ, et al. Among authors: barton nw. Mol Genet Metab. 2017 Jan-Feb;120(1-2):1-7. doi: 10.1016/j.ymgme.2016.10.010. Epub 2016 Nov 12. Mol Genet Metab. 2017. PMID: 27866832
Retroviral transfer of the glucocerebrosidase gene into CD34+ cells from patients with Gaucher disease: in vivo detection of transduced cells without myeloablation.
Dunbar CE, Kohn DB, Schiffmann R, Barton NW, Nolta JA, Esplin JA, Pensiero M, Long Z, Lockey C, Emmons RV, Csik S, Leitman S, Krebs CB, Carter C, Brady RO, Karlsson S. Dunbar CE, et al. Among authors: barton nw. Hum Gene Ther. 1998 Nov 20;9(17):2629-40. doi: 10.1089/hum.1998.9.17-2629. Hum Gene Ther. 1998. PMID: 9853529 Clinical Trial.
Outcome of partial splenectomy for type I Gaucher disease.
Zimran A, Elstein D, Schiffmann R, Abrahamov A, Goldberg M, Bar-Maor JA, Brady RO, Guzzetta PC, Barton NW. Zimran A, et al. Among authors: barton nw. J Pediatr. 1995 Apr;126(4):596-7. doi: 10.1016/s0022-3476(95)70358-6. J Pediatr. 1995. PMID: 7699540
Physiological characterization of neuropathy in Fabry's disease.
Luciano CA, Russell JW, Banerjee TK, Quirk JM, Scott LJ, Dambrosia JM, Barton NW, Schiffmann R. Luciano CA, et al. Among authors: barton nw. Muscle Nerve. 2002 Nov;26(5):622-9. doi: 10.1002/mus.10236. Muscle Nerve. 2002. PMID: 12402283
91 results