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See Latest ArticlesSynthesis and radiosynthesis of N5-[18F]fluoroethyl-Pirenzepine and its metabolite N5-[18F]fluoroethyl-LS 75
Journal of Labelled Compounds and Radiopharmaceuticals, 11/09/09
Riss PJ et al. – Compound 3 did not show activity as an inhibitor of PARP–1. Contrary, 4 displays moderate PARP–1 inhibition potency. The new radiotracer [18F]–4 can be applied for molecular imaging using autoradiography and PET.
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A Comparison Between Diagnostic I-123 and Posttherapy I-131 Scans in the Detection of Remnant and Locoregional Thyroid Disease
Clinical Nuclear Medicine , 11/25/09
Comparison of 18F-Fluoro-L-DOPA, 18F-Fluoro-Deoxyglucose, and 18F-Fluorodopamine PET and 123I-MIBG Scintigraphy in the Localization of Pheochromocytoma and Paraganglioma
Journal of Clinical Endocrinology and Metabolism, 11/12/09
Use of 18F-FDG-PET in the diagnosis of endoprosthetic loosening of knee and hip implants
Archives of Orthopaedic and Trauma Surgery, 11/10/09
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