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- Alglucosidase_alfa abstract "Alglucosidase alfa (Lumizyme, Myozyme, Genzyme) is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD).Chemically speaking, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha-glucosidase. It is the first drug available to treat this disease.".
- Alglucosidase_alfa atcPrefix "A16".
- Alglucosidase_alfa atcSuffix "AB07".
- Alglucosidase_alfa casNumber "420794-05-0".
- Alglucosidase_alfa drugbank "DB01272".
- Alglucosidase_alfa fdaUniiCode "DTI67O9503".
- Alglucosidase_alfa iupacName "Human glucosidase, prepro-α-[199-arginine,223-histidine]".
- Alglucosidase_alfa wikiPageExternalLink www.myozyme.com.
- Alglucosidase_alfa wikiPageExternalLink mtap_pt.asp.
- Alglucosidase_alfa wikiPageID "13081045".
- Alglucosidase_alfa wikiPageLength "5323".
- Alglucosidase_alfa wikiPageOutDegree "20".
- Alglucosidase_alfa wikiPageRevisionID "705669858".
- Alglucosidase_alfa wikiPageWikiLink Allergy.
- Alglucosidase_alfa wikiPageWikiLink Alpha-glucosidase.
- Alglucosidase_alfa wikiPageWikiLink Category:Medical_treatments.
- Alglucosidase_alfa wikiPageWikiLink Category:Orphan_drugs.
- Alglucosidase_alfa wikiPageWikiLink Enzyme_replacement_therapy.
- Alglucosidase_alfa wikiPageWikiLink Fever.
- Alglucosidase_alfa wikiPageWikiLink Food_and_Drug_Administration.
- Alglucosidase_alfa wikiPageWikiLink Genzyme.
- Alglucosidase_alfa wikiPageWikiLink Glycogen_storage_disease_type_II.
- Alglucosidase_alfa wikiPageWikiLink Heart_failure.
- Alglucosidase_alfa wikiPageWikiLink Infection.
- Alglucosidase_alfa wikiPageWikiLink Lysosomal_storage_disease.
- Alglucosidase_alfa wikiPageWikiLink Orphan_drug.
- Alglucosidase_alfa wikiPageWikiLink Pneumonia.
- Alglucosidase_alfa wikiPageWikiLink Rare_disease.
- Alglucosidase_alfa wikiPageWikiLink Respiratory_failure.
- Alglucosidase_alfa wikiPageWikiLink Structural_analog.
- Alglucosidase_alfa wikiPageWikiLink United_States_dollar.
- Alglucosidase_alfa wikiPageWikiLinkText "Alglucosidase alfa".
- Alglucosidase_alfa wikiPageWikiLinkText "alglucosidase alfa".
- Alglucosidase_alfa atcPrefix "A16".
- Alglucosidase_alfa atcSuffix "AB07".
- Alglucosidase_alfa c "4758".
- Alglucosidase_alfa casNumber "420794".
- Alglucosidase_alfa chemspiderid "none".
- Alglucosidase_alfa drugbank "DB01272".
- Alglucosidase_alfa h "7262".
- Alglucosidase_alfa iupacName "Human glucosidase, prepro-α-[199-arginine,223-histidine]".
- Alglucosidase_alfa kegg "D03207".
- Alglucosidase_alfa legalStatus "FDA approved for children".
- Alglucosidase_alfa molecularWeightRound "0".
- Alglucosidase_alfa n "1274".
- Alglucosidase_alfa o "1369".
- Alglucosidase_alfa routesOfAdministration "Intravenous".
- Alglucosidase_alfa s "35".
- Alglucosidase_alfa unii "DTI67O9503".
- Alglucosidase_alfa verifiedfields "changed".
- Alglucosidase_alfa verifiedrevid "477314655".
- Alglucosidase_alfa watchedfields "changed".
- Alglucosidase_alfa wikiPageUsesTemplate Template:Cascite.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Chemspidercite.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Drugbankcite.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Drugbox.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Drugs.com.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Fdacite.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Keggcite.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Other_alimentary_tract_and_metabolism_products.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Reflist.
- Alglucosidase_alfa wikiPageUsesTemplate Template:Research_help.
- Alglucosidase_alfa subject Category:Medical_treatments.
- Alglucosidase_alfa subject Category:Orphan_drugs.
- Alglucosidase_alfa hypernym Drug.
- Alglucosidase_alfa type ChemicalSubstance.
- Alglucosidase_alfa type Drug.
- Alglucosidase_alfa type Chemical.
- Alglucosidase_alfa type Drug.
- Alglucosidase_alfa type Redirect.
- Alglucosidase_alfa type ChemicalObject.
- Alglucosidase_alfa type Thing.
- Alglucosidase_alfa type Q8386.
- Alglucosidase_alfa comment "Alglucosidase alfa (Lumizyme, Myozyme, Genzyme) is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD).Chemically speaking, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha-glucosidase. It is the first drug available to treat this disease.".
- Alglucosidase_alfa label "Alglucosidase alfa".
- Alglucosidase_alfa sameAs Q2919537.
- Alglucosidase_alfa sameAs Alglucosidase_Alfa.
- Alglucosidase_alfa sameAs アルグルコシダーゼ_アルファ.
- Alglucosidase_alfa sameAs Alglucosidase_alfa.
- Alglucosidase_alfa sameAs m.03by4dy.
- Alglucosidase_alfa sameAs Alglukozidaza_alfa.
- Alglucosidase_alfa sameAs Alglukozidaza_alfa.
- Alglucosidase_alfa sameAs Q2919537.
- Alglucosidase_alfa wasDerivedFrom Alglucosidase_alfa?oldid=705669858.
- Alglucosidase_alfa homepage www.myozyme.com.
- Alglucosidase_alfa isPrimaryTopicOf Alglucosidase_alfa.