Idursulfase for the treatment of mucopolvsaccharidosis II

Expert Opinion on Pharmacotherapy

Volumn 9, Issue 2, 2008, Pages 311-317

  Clarke, Lorne A ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Glycoprotein; Glycosaminoglycan; Hunter syndrome; Lysosomal disease; Mucopolysaccharidosis; Recombinant protein; Sulfatase

Indexed keywords

ANTIHISTAMINIC AGENT; CORTICOSTEROID; IDURONATE 2 SULFATASE; OXYGEN; PLACEBO; RECOMBINANT PROTEIN;

ARTICLE; CANADA; CLINICAL PROTOCOL; CLINICAL TRIAL; CONTINUOUS INFUSION; DISEASE MODEL; DISTRIBUTION VOLUME; DRUG APPROVAL; DRUG DOSE COMPARISON; DRUG EFFICACY; DRUG HALF LIFE; DRUG MECHANISM; DRUG SAFETY; DRUG SYNTHESIS; DRUG TOLERABILITY; EUROPE; GENETIC DISORDER; GLYCOSYLATION; HUMAN; HUNTER SYNDROME; INJECTION SITE REACTION; JAPAN; NONHUMAN; RECOMMENDED DRUG DOSE; RESPIRATORY DISTRESS; SINGLE DRUG DOSE; UNITED STATES; ANIMAL; METABOLISM; REVIEW; TREATMENT OUTCOME;

ANIMALS; CLINICAL TRIALS AS TOPIC; HUMANS; IDURONATE SULFATASE; MUCOPOLYSACCHARIDOSIS II; TREATMENT OUTCOME;

EID: 39049159592     PISSN: 14656566     EISSN: None     Source Type: Journal    
DOI: 10.1517/14656566.9.2.311     Document Type: Article

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