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Enzyme replacement therapy for lysosomal storage diseases.
Lachmann, Robin H.
Affiliation
  • Lachmann RH; Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, Queen Square, London, UK. robin.lachmann@uclh.nhs.uk
Curr Opin Pediatr ; 23(6): 588-93, 2011 Dec.
Article in En | MEDLINE | ID: mdl-21946346
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lysosomal Storage Diseases / Enzyme Replacement Therapy / Enzyme Therapy Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Curr Opin Pediatr Journal subject: PEDIATRIA Year: 2011 Document type: Article Affiliation country: United kingdom Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lysosomal Storage Diseases / Enzyme Replacement Therapy / Enzyme Therapy Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Curr Opin Pediatr Journal subject: PEDIATRIA Year: 2011 Document type: Article Affiliation country: United kingdom Country of publication: United States