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Pain in adult patients with Pompe disease

  • Published:2013-08 Issue:4 Volume:109 Page:371-376
  • ISSN:1096-7192
  • Container-title:Molecular Genetics and Metabolism
  • language:en
  • Short-container-title:Molecular Genetics and Metabolism

Author:

Güngör D.,Schober A.K.,Kruijshaar M.E.,Plug I.,Karabul N.,Deschauer M.,van Doorn P.A.,van der Ploeg A.T.,Schoser B.,Hanisch F.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference35 articles.

1. Glycogen storage disease type II: acid alpha-glucosidase (acid maltase) deficiency;Hirschhorn,2001

2. Acid maltase deficiency;Engel,2004

3. Enzyme replacement therapy in classical infantile Pompe disease: results of a ten-month follow-up study;Klinge;Neuropediatrics,2005

4. Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: results of a phase II clinical trial;Klinge;Neuromuscul. Disord.,2005

5. Recombinant human alpha-glucosidase from rabbit milk in Pompe patients;Van den Hout;Lancet,2000
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