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Outcomes after 18 months of eliglustat therapy in treatment-naïve adults with Gaucher disease type 1: The phase 3 ENGAGE trial.
Am J Hematol. 2017 Nov;92(11):1170-1176. doi: 10.1002/ajh.24877. Epub 2017 Oct 3.
Am J Hematol. 2017.
PMID: 28762527
Free PMC article.
Clinical Trial.
Eliglustat maintains long-term clinical stability in patients with Gaucher disease type 1 stabilized on enzyme therapy.
Cox TM, Drelichman G, Cravo R, Balwani M, Burrow TA, Martins AM, Lukina E, Rosenbloom B, Goker-Alpan O, Watman N, El-Beshlawy A, Kishnani PS, Pedroso ML, Gaemers SJM, Tayag R, Peterschmitt MJ.
Cox TM, et al. Among authors: tayag r.
Blood. 2017 Apr 27;129(17):2375-2383. doi: 10.1182/blood-2016-12-758409. Epub 2017 Feb 6.
Blood. 2017.
PMID: 28167660
Free PMC article.
Clinical Trial.
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Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study.
Khan N, Cabo R, Tan WH, Tayag R, Bird LM.
Khan N, et al. Among authors: tayag r.
Mol Genet Genomic Med. 2019 Jul;7(7):e00734. doi: 10.1002/mgg3.734. Epub 2019 May 14.
Mol Genet Genomic Med. 2019.
PMID: 31090212
Free PMC article.
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An observational study of pediatric healthcare burden in Angelman syndrome: results from a real-world study.
Khan N, Cabo R, Tan WH, Tayag R, Bird LM.
Khan N, et al. Among authors: tayag r.
Orphanet J Rare Dis. 2019 Nov 4;14(1):239. doi: 10.1186/s13023-019-1210-6.
Orphanet J Rare Dis. 2019.
PMID: 31684986
Free PMC article.
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