Norman W Barton, MD, PhD

Affiliations: 
2013-2018 Neuroscience Shire 
 2018- Rare Diseases Takeda 
Area:
Leukodystrophies, Neurochemistry
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"Norman Barton"
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Publications

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Mistry PK, Lopez G, Schiffmann R, et al. (2016) Gaucher disease circa 2016: Progress and ongoing challenges. Molecular Genetics and Metabolism
Desnick RJ, Barton NW, Furbish S, et al. (2016) Roscoe Owen Brady, MD: Remembrances of co-investigators and colleagues. Molecular Genetics and Metabolism
Ben Turkia H, Gonzalez DE, Barton NW, et al. (2013) Velaglucerase alfa enzyme replacement therapy compared with imiglucerase in patients with Gaucher disease. American Journal of Hematology. 88: 179-84
Gonzalez DE, Turkia HB, Lukina EA, et al. (2013) Enzyme replacement therapy with velaglucerase alfa in Gaucher disease: Results from a randomized, double-blind, multinational, Phase 3 study. American Journal of Hematology. 88: 166-71
Mehta A, Turkia HB, Gonzalez D, et al. (2011) Two-Year Safety and Tolerability of Velaglucerase Alfa in Patients with Type 1 Gaucher Disease, Including Patients Switched From Imiglucerase: Phase III Trial HGT-GCB-039 and Extension, Blood. 118: 3214-3214
Luciano CA, Russell JW, Banerjee TK, et al. (2002) Physiological characterization of neuropathy in Fabry's disease. Muscle & Nerve. 26: 622-9
Schiffmann R, Mankin H, Dambrosia JM, et al. (2002) Decreased bone density in splenectomized Gaucher patients receiving enzyme replacement therapy Blood Cells, Molecules, and Diseases. 28: 288-296
Altarescu G, Hill S, Wiggs E, et al. (2001) The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's disease. The Journal of Pediatrics. 138: 539-47
Altarescu G, Schiffmann R, Parker CC, et al. (2000) Comparative efficacy of dose regimens in enzyme replacement therapy of type I Gaucher disease. Blood Cells, Molecules & Diseases. 26: 285-90
Scott LJ, Griffin JW, Luciano C, et al. (1999) Quantitative analysis of epidermal innervation in Fabry disease. Neurology. 52: 1249-54
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