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Journal Abstract Search

338 related items for PubMed ID: 29289479

  • 21. Effect of alglucosidase alfa dosage on survival and walking ability in patients with classic infantile Pompe disease: a multicentre observational cohort study from the European Pompe Consortium.
    Ditters IAM, Huidekoper HH, Kruijshaar ME, Rizopoulos D, Hahn A, Mongini TE, Labarthe F, Tardieu M, Chabrol B, Brassier A, Parini R, Parenti G, van der Beek NAME, van der Ploeg AT, van den Hout JMP, European Pompe Consortium project group on classic infantile Pompe disease.
    Lancet Child Adolesc Health; 2022 Jan; 6(1):28-37. PubMed ID: 34822769
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  • 22. Effect of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in 12 patients with advanced late-onset Pompe disease.
    Papadopoulos C, Orlikowski D, Prigent H, Lacour A, Tard C, Furby A, Praline J, Solé G, Hogrel JY, De Antonio M, Semplicini C, Deibener-Kaminsky J, Kaminsky P, Eymard B, Taouagh N, Perniconi B, Hamroun D, Laforêt P, French Pompe Study Group.
    Mol Genet Metab; 2017 Sep; 122(1-2):80-85. PubMed ID: 28648663
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  • 29. Enzyme replacement therapy in late-onset Pompe disease: a systematic literature review.
    Toscano A, Schoser B.
    J Neurol; 2013 Apr; 260(4):951-9. PubMed ID: 22926164
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  • 30. Immune responses to alglucosidase in infantile Pompe disease: recommendations from an Italian pediatric expert panel.
    Gragnaniello V, Deodato F, Gasperini S, Donati MA, Canessa C, Fecarotta S, Pascarella A, Spadaro G, Concolino D, Burlina A, Parenti G, Strisciuglio P, Fiumara A, Casa RD.
    Ital J Pediatr; 2022 Mar 05; 48(1):41. PubMed ID: 35248118
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  • 38. Cessation and resuming of alglucosidase alfa in Pompe disease: a retrospective analysis.
    Hundsberger T, Rösler KM, Findling O.
    J Neurol; 2014 Sep 05; 261(9):1684-90. PubMed ID: 24923245
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