Použitá literatúra

  • Pompe JC Over idiopathische hypertrofie van het hart. Ned Tijdschr Geneeskd 1932;76:304‐311.
  • Hirschhorn R, Reuser AJ. Glycogen Storage Disease Type II: Acid α‐Glucosidase (Acid Maltase) Deficiency. In: Valle D, Beaudet AL, Vogelstein B, Kinzler KW, Antonarakis SE, Ballabio A, Gibson K, Mitchell G., eds. The Online Metabolic and Molecular Bases of Inherited Disease. OMMBID. Available at: http://ommbid.mhmedical.com/book.aspx?bookid=971. Accessed February 2015.
  • van der Ploeg AT, Reuser AJ Pompe's disease. Lancet 2008;372(9646):1342‐53.
  • Kishnani PS, Howell RR Pompe disease in infants and children. J Pediatr 2004;144(5 Suppl):S35‐S43.
  • Hagemans ML, Winkel LP, Van Doorn PA et al. Clinical manifestation and natural course of late‐onset Pompe’s disease in 54 Dutch patients. Brain 2005;128:671‐7.
  • Wokke J, Escolar D, Pestronk A et al. Clinical features of late‐onset Pompe disease: A prospective cohort study. Muscle Nerve 2008;38:1236‐45.