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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 wikiPageRevisionID "604987112".
- Alglucosidase_alfa atcPrefix "A16".
- Alglucosidase_alfa atcSuffix "AB07".
- Alglucosidase_alfa c "4758".
- Alglucosidase_alfa casNumber "420794".
- Alglucosidase_alfa chemspiderid "NA".
- Alglucosidase_alfa drugbank "DB01272".
- Alglucosidase_alfa h "7262".
- Alglucosidase_alfa hasPhotoCollection Alglucosidase_alfa.
- Alglucosidase_alfa iupacName "Human glucosidase, prepro-α-[199-arginine,223-histidine]".
- Alglucosidase_alfa kegg "D03207".
- Alglucosidase_alfa legalStatus "FDA approved for children".
- Alglucosidase_alfa molecularWeight "105338".
- 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 subject Category:Medical_treatments.
- Alglucosidase_alfa subject Category:Orphan_drugs.
- Alglucosidase_alfa type Abstraction100002137.
- Alglucosidase_alfa type Act100030358.
- Alglucosidase_alfa type Activity100407535.
- Alglucosidase_alfa type Care100654885.
- Alglucosidase_alfa type Event100029378.
- Alglucosidase_alfa type MedicalTreatments.
- Alglucosidase_alfa type PsychologicalFeature100023100.
- Alglucosidase_alfa type Treatment100658082.
- Alglucosidase_alfa type Work100575741.
- Alglucosidase_alfa type YagoPermanentlyLocatedEntity.
- Alglucosidase_alfa type Drug.
- Alglucosidase_alfa type DrugProduct.
- Alglucosidase_alfa type FunctionalSubstance.
- 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 label "Alglucosidase alfa".
- Alglucosidase_alfa label "アルグルコシダーゼ アルファ".
- 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 Q2919537.
- Alglucosidase_alfa sameAs Q2919537.
- Alglucosidase_alfa sameAs DB01272.
- Alglucosidase_alfa sameAs Alglucosidase_alfa.
- Alglucosidase_alfa wasDerivedFrom Alglucosidase_alfa?oldid=604987112.
- Alglucosidase_alfa homepage www.myozyme.com.
- Alglucosidase_alfa isPrimaryTopicOf Alglucosidase_alfa.