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PUBMED FOR HANDHELDS

Journal Abstract Search

306 related items for PubMed ID: 17703370

  • 1.
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  • 2. Baseline characteristics and outcome in Romanian patients with Gaucher disease type 1.
    Grigorescu-Sido P, Drugan C, Alkhzouz C, Zimmermann A, Coldea C, Denes C, Grigorescu MD, Cret V, Bucerzan S.
    Eur J Intern Med; 2010 Apr; 21(2):104-13. PubMed ID: 20206881
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  • 3. [Alglucerase treatment of type I Gaucher's disease. Preliminary results in Spain. Spanish Group on Gaucher's Disease].
    Pérez-Calvo JI, Giraldo P, Giralt M.
    Sangre (Barc); 1997 Jun; 42(3):189-94. PubMed ID: 9381260
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  • 4. [A retrospective study on enzyme replacement therapy in patients with Gaucher disease].
    Duan YL, Zhang YH, Zang Y, Shi HP, Zhang WM, Hu YM.
    Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):653-6. PubMed ID: 17217655
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  • 5. Enzyme therapy in Gaucher disease type 1: dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months.
    Pastores GM, Sibille AR, Grabowski GA.
    Blood; 1993 Jul 15; 82(2):408-16. PubMed ID: 8392397
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  • 7. Enzyme replacement and substrate reduction therapy for Gaucher disease.
    Shemesh E, Deroma L, Bembi B, Deegan P, Hollak C, Weinreb NJ, Cox TM.
    Cochrane Database Syst Rev; 2015 Mar 27; 2015(3):CD010324. PubMed ID: 25812601
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  • 8. Plasma chitotriosidase activity versus CCL18 level for assessing type I Gaucher disease severity: protocol for a systematic review with meta-analysis of individual participant data.
    Raskovalova T, Deegan PB, Yang R, Pavlova E, Stirnemann J, Labarère J, Zimran A, Mistry PK, Berger M.
    Syst Rev; 2017 Apr 20; 6(1):87. PubMed ID: 28427477
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  • 9. Velaglucerase alfa for the management of type 1 Gaucher disease.
    Morris JL.
    Clin Ther; 2012 Feb 20; 34(2):259-71. PubMed ID: 22264444
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  • 10. Outcomes after 8 years of eliglustat therapy for Gaucher disease type 1: Final results from the Phase 2 trial.
    Lukina E, Watman N, Dragosky M, Lau H, Avila Arreguin E, Rosenbaum H, Zimran A, Foster MC, Gaemers SJM, Peterschmitt MJ.
    Am J Hematol; 2019 Jan 20; 94(1):29-38. PubMed ID: 30264864
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  • 11. Serum chitotriosidase activity in Gaucher patients on enzyme replacement therapy (ERT).
    Czartoryska B, Tylki-Szymańska A, Górska D.
    Clin Biochem; 1998 Jul 20; 31(5):417-20. PubMed ID: 9721443
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  • 12. Enzyme replacement therapy for Gaucher disease in Australia.
    Goldblatt J, Szer J, Fletcher JM, McGill J, Rowell JA, Wilson M.
    Intern Med J; 2005 Mar 20; 35(3):156-61. PubMed ID: 15737135
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  • 13. Effect of treatment on biclonal gammopathy associated with Gaucher disease.
    Decaux O, Ruelland A, Grosbois B.
    J Inherit Metab Dis; 2007 Oct 20; 30(5):824. PubMed ID: 17879146
    [Abstract] [Full Text] [Related]

  • 14. The clinical course of untreated Gaucher disease in 22 patients over 10 years: hematological and skeletal manifestations.
    Piran S, Roberts A, Patterson MA, Amato D.
    Blood Cells Mol Dis; 2009 Oct 20; 43(3):289-93. PubMed ID: 19793665
    [Abstract] [Full Text] [Related]

  • 15. Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry.
    Weinreb NJ, Charrow J, Andersson HC, Kaplan P, Kolodny EH, Mistry P, Pastores G, Rosenbloom BE, Scott CR, Wappner RS, Zimran A.
    Am J Med; 2002 Aug 01; 113(2):112-9. PubMed ID: 12133749
    [Abstract] [Full Text] [Related]

  • 16. Therapeutic goals in Gaucher disease.
    Mistry P, Germain DP.
    Rev Med Interne; 2006 Mar 01; 27 Suppl 1():S30-8. PubMed ID: 16644400
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  • 20. Enzyme replacement therapy with imiglucerase in Taiwanese patients with type I Gaucher disease.
    Hsu CC, Chien YH, Lai MY, Hwu WL.
    J Formos Med Assoc; 2002 Sep 01; 101(9):627-31. PubMed ID: 12645190
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