Please use this identifier to cite or link to this item: http://elibrary.nnra.gov.ng/jspui/handle/123456789/684
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dc.contributor.authorIAEA-
dc.date.accessioned2021-06-30T10:15:36Z-
dc.date.available2021-06-30T10:15:36Z-
dc.date.issued2021-
dc.identifier.urihttp://elibrary.nnra.gov.ng/jspui/handle/123456789/684-
dc.descriptionTherapeutic radiopharmaceuticals play a major role in today’s nuclear medicine, especially in the treatment of cancer. They have long been applied in ‘radiation synovectomy’, or, more briefly, ‘radiosynovectomy’ (RSV). In recent decades, the production and quality control of radiopharmaceuticals for use in RSV has moved from simple 32P colloids to recently developed matrixes labelled with short and medium range beta emitters. RSV is a well established technique with growing applications worldwide. However, the lack of generic and peer reviewed production, quality control and clinical application guidelines and recommendations is a major concern for their application in human patients.en_US
dc.language.isoenen_US
dc.publisherNNRA Libraryen_US
dc.relation.ispartofseriesNO-3;-
dc.subjectRadiopharmaceuticalsen_US
dc.subjectSynovectomyen_US
dc.subjectNuclear medicine.en_US
dc.subjectRadioisotopes — Therapeutic useen_US
dc.titleProduction Qualilty Control And Clinical Applications Of Radiosynovectomy Agentsen_US
dc.typeBooken_US
Appears in Collections:Human Health

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