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Journal Abstract Search

491 related items for PubMed ID: 18525427

  • 21.
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  • 22. Enzyme replacement therapy in severe adult-onset glycogen storage disease type II.
    Ravaglia S, Danesino C, Pichiecchio A, Repetto A, Poloni GU, Rossi M, Fratino P, Moglia A, Costa A.
    Adv Ther; 2008 Aug; 25(8):820-9. PubMed ID: 18704279
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  • 24. Pompe disease: a neuromuscular disease with respiratory muscle involvement.
    Mellies U, Lofaso F.
    Respir Med; 2009 Apr; 103(4):477-84. PubMed ID: 19131232
    [Abstract] [Full Text] [Related]

  • 25. New therapeutic approaches for Pompe disease: enzyme replacement therapy and beyond.
    Kishnani PS, Beckemeyer AA.
    Pediatr Endocrinol Rev; 2014 Sep; 12 Suppl 1():114-24. PubMed ID: 25345093
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  • 26. [Myopathy associated with respiratory insufficiency: diagnostic difficulties in adult-onset Pompe disease].
    Merkli H, Pál E, Nagy F, Horváth R, Várdi VK, Komoly S, Illés Z.
    Orv Hetil; 2006 Jul 30; 147(30):1421-4. PubMed ID: 16977780
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  • 27. Differential muscular glycogen clearance after enzyme replacement therapy in a mouse model of Pompe disease.
    Hawes ML, Kennedy W, O'Callaghan MW, Thurberg BL.
    Mol Genet Metab; 2007 Aug 30; 91(4):343-51. PubMed ID: 17572127
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  • 31. Correlation of acid alpha-glucosidase and glycogen content in skin fibroblasts with age of onset in Pompe disease.
    Umapathysivam K, Hopwood JJ, Meikle PJ.
    Clin Chim Acta; 2005 Nov 30; 361(1-2):191-8. PubMed ID: 15993875
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  • 33. Significance of early diagnosis and treatment of adult late-onset Pompe disease on the effectiveness of enzyme replacement therapy in improving muscle strength and respiratory function: a case report.
    Mir M, Rouhani K, Rouhani K, Hassani M, Damirchi M, Yazdansetad S, Aghaei M.
    J Med Case Rep; 2024 Oct 08; 18(1):486. PubMed ID: 39375771
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  • 34. Enzyme replacement therapy in late-onset Pompe's disease: a three-year follow-up.
    Winkel LP, Van den Hout JM, Kamphoven JH, Disseldorp JA, Remmerswaal M, Arts WF, Loonen MC, Vulto AG, Van Doorn PA, De Jong G, Hop W, Smit GP, Shapira SK, Boer MA, van Diggelen OP, Reuser AJ, Van der Ploeg AT.
    Ann Neurol; 2004 Apr 08; 55(4):495-502. PubMed ID: 15048888
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  • 35. The new era of Pompe disease: advances in the detection, understanding of the phenotypic spectrum, pathophysiology, and management.
    Kishnani PS, Beckemeyer AA, Mendelsohn NJ.
    Am J Med Genet C Semin Med Genet; 2012 Feb 15; 160C(1):1-7. PubMed ID: 22253049
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  • 36. Advances in diagnosis and management of Pompe disease.
    Davison JE.
    J Mother Child; 2020 Oct 02; 24(2):3-8. PubMed ID: 33554498
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  • 37. [Treatment of Pompe's disease with recombinant enzymes].
    Van Hove JL.
    Verh K Acad Geneeskd Belg; 1998 Oct 02; 60(4):347-57. PubMed ID: 9883081
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  • 38. Clinical guidelines for late-onset Pompe disease.
    Barba-Romero MA, Barrot E, Bautista-Lorite J, Gutierrez-Rivas E, Illa I, Jimenez LM, Ley-Martos M, Lopez de Munain A, Pardo J, Pascual-Pascual SI, Perez-Lopez J, Solera J, Vilchez-Padilla JJ.
    Rev Neurol; 2012 Apr 16; 54(8):497-507. PubMed ID: 22492103
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