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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

300 related items for PubMed ID: 19507165

  • 1. Miglustat (Zavesca) in type 1 Gaucher disease: 5-year results of a post-authorisation safety surveillance programme.
    Hollak CE, Hughes D, van Schaik IN, Schwierin B, Bembi B.
    Pharmacoepidemiol Drug Saf; 2009 Sep; 18(9):770-7. PubMed ID: 19507165
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  • 3. Effect of miglustat on bone disease in adults with type 1 Gaucher disease: a pooled analysis of three multinational, open-label studies.
    Pastores GM, Elstein D, Hrebícek M, Zimran A.
    Clin Ther; 2007 Aug; 29(8):1645-54. PubMed ID: 17919546
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  • 4. Results from a 9-year Intensive Safety Surveillance Scheme (IS(3) ) in miglustat (Zavesca(®) )-treated patients.
    Brand M, Muller A, Alsop J, van Schaik IN, Bembi B, Hughes D.
    Pharmacoepidemiol Drug Saf; 2015 Mar; 24(3):329-33. PubMed ID: 25656910
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  • 6. Miglustat therapy in type 1 Gaucher disease: clinical and safety outcomes in a multicenter retrospective cohort study.
    Kuter DJ, Mehta A, Hollak CE, Giraldo P, Hughes D, Belmatoug N, Brand M, Muller A, Schaaf B, Giorgino R, Zimran A.
    Blood Cells Mol Dis; 2013 Aug; 51(2):116-24. PubMed ID: 23683771
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  • 9. Goal-oriented therapy with miglustat in Gaucher disease.
    Pastores GM, Giraldo P, Chérin P, Mehta A.
    Curr Med Res Opin; 2009 Jan; 25(1):23-37. PubMed ID: 19210136
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  • 10. Twelve years of experience with miglustat in the treatment of type 1 Gaucher disease: The Spanish ZAGAL project.
    Giraldo P, Andrade-Campos M, Alfonso P, Irun P, Atutxa K, Acedo A, Barez A, Blanes M, Diaz-Morant V, Fernández-Galán MA, Franco R, Gil-Cortes C, Giner V, Ibañez A, Latre P, Loyola I, Luño E, Hernández-Martin R, Medrano-Engay B, Puerta J, Roig I, de la Serna J, Salamero O, Villalón L, Pocovi M.
    Blood Cells Mol Dis; 2018 Feb; 68():173-179. PubMed ID: 27836529
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  • 11. Switching from imiglucerase to miglustat for the treatment of French patients with Gaucher disease type 1: a case series.
    Serratrice C, Swiader L, Serratrice J.
    J Med Case Rep; 2015 Jun 23; 9():146. PubMed ID: 26100396
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  • 12. Changes in the atherogenic profile of patients with type 1 Gaucher disease after miglustat therapy.
    Puzo J, Alfonso P, Irun P, Gervas J, Pocovi M, Giraldo P.
    Atherosclerosis; 2010 Apr 23; 209(2):515-9. PubMed ID: 19959168
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  • 13. Substrate reduction therapy.
    Platt FM, Jeyakumar M.
    Acta Paediatr; 2008 Apr 23; 97(457):88-93. PubMed ID: 18339196
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  • 16. Evaluation of miglustat as maintenance therapy after enzyme therapy in adults with stable type 1 Gaucher disease: a prospective, open-label non-inferiority study.
    Cox TM, Amato D, Hollak CE, Luzy C, Silkey M, Giorgino R, Steiner RD, Miglustat Maintenance Study Group.
    Orphanet J Rare Dis; 2012 Dec 27; 7():102. PubMed ID: 23270487
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  • 17. Long-term miglustat therapy in children with Niemann-Pick disease type C.
    Patterson MC, Vecchio D, Jacklin E, Abel L, Chadha-Boreham H, Luzy C, Giorgino R, Wraith JE.
    J Child Neurol; 2010 Mar 27; 25(3):300-5. PubMed ID: 19822772
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  • 18. Real-world clinical experience with long-term miglustat maintenance therapy in type 1 Gaucher disease: the ZAGAL project.
    Giraldo P, Alfonso P, Atutxa K, Fernández-Galán MA, Barez A, Franco R, Alonso D, Martin A, Latre P, Pocovi M.
    Haematologica; 2009 Dec 27; 94(12):1771-5. PubMed ID: 19608672
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  • 19. Successful switch from enzyme replacement therapy to miglustat in an adult patient with type 1 Gaucher disease: a case report.
    Giuffrida G, Lombardo R, Di Francesco E, Parrinello L, Di Raimondo F, Fiumara A.
    J Med Case Rep; 2016 Nov 08; 10(1):315. PubMed ID: 27821156
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