alglucerase

alglucerase
al·glu·ce·rase .al-'glü-sə-.rās n modified human glucocerebrosidase administered for enzyme replacement therapy in the treatment of Gaucher's disease see ceredase

* * *

al·glu·cer·ase (al-glooґsər-ās″) a modified form of β-glucocerebrosidase, prepared from pooled human placental tissue, used to replace glucocerebrosidase (glucosylceramidase) in the treatment of type 1 Gaucher's disease; administered by intravenous infusion.

Medical dictionary. 2011.

Игры ⚽ Нужен реферат?

Look at other dictionaries:

  • Alglucerase — Systematic (IUPAC) name Human beta glucocerebrosidase Clinical data AHFS/Drugs.com monograph MedlinePlus …   Wikipedia

  • Ceredase — Cer·e·dase ser ə .dās trademark used for a preparation of alglucerase * * * Cer·e·dase (serґə dās) trademark for a preparation of alglucerase …   Medical dictionary

  • Carnitine — Systematic (IUPAC) name 3 hydroxy 4 (trimethylazaniumyl)butanoate Clinical data AHFS/Drugs.com …   Wikipedia

  • ATC code A16 — is a division of the Anatomical Therapeutic Chemical Classification System and part of the A Alimentary tract and metabolism section.A16A Other alimentary tract and metabolism products*A16AA Amino acids and derivatives:A16AA01… …   Wikipedia

  • Tetrahydrobiopterin — Systematic (IUPAC) name (6R) 2 Amino 6 [(1R,2S) 1,2 dihydroxypropyl] 5,6,7,8 tetrahydropteridin 4(1H) one Clinical data …   Wikipedia

  • Imiglucerase — Systematic (IUPAC) name Human Beta glucocerebrosidase Clinical data AHFS/Drugs.com monograph MedlinePlus …   Wikipedia

  • Nitisinone — Systematic (IUPAC) name 2 [2 nitro 4 (trifluoromethyl)benzoyl] cyclohexane 1,3 dione Clinical data AHFS/Drugs.com …   Wikipedia

  • Miglustat — Systematic (IUPAC) name (2R,3R,4R,5S) 1 butyl 2 (hydroxymethyl)piperidine 3,4,5 triol Clinical data AHFS/Drugs.co …   Wikipedia

  • Alglucosidase alfa — Systematic (IUPAC) name Human glucosidase, prepro α [199 arginine,223 histidine] [1] Clinical data AHFS/Drugs.com …   Wikipedia

  • Enzyme replacement therapy — Die Enzymersatztherapie (EET oder ERT von engl. Enzyme Replacement Therapy) ist ein therapeutisches Verfahren zur Behandlung von Enzymdefekten bei lysosomalen Speicherkrankheiten. Den Patienten werden dabei per Infusion oder Injektion… …   Deutsch Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”