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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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Bilateral rapidly destructive arthrosis of the hip joint resulting from subchondral fracture with superimposed secondary osteonecrosis
Skeletal Radiology, 12/09/09
Diffuse arachnoid ossification and multiple arachnoid cysts presenting with progressive thoracic myelopathy
Skeletal Radiology, 12/09/09
Optimization of flow reserve measurement using SPECT technology to evaluate the determinants of coronary microvascular dysfunction in diabetes
European Journal of Nuclear Medicine & Molecular Imaging, 12/09/09
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