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Nuclear Medicine in Tropical and Infectious Diseases (Developments in Nuclear Medicine): Medicine & Health Science Books.
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Also discussed is the potential for imaging fungal cell wall structure and implications for the development of tracers. The authors describe the potential of glucans, chitins, and mannoproteins, as well as of phospholipids and other components, as targets in the cell wall.

Day in the Life of a DOCTOR: Vlogging Infectious Diseases Rotation (ft. Q&A Memorization Tips)

A discussion follows about cutting-edge research on molecular imaging of mononuclear cell—mediated inflammation using the anti—induced endothelial cell adhesion molecule and other adhesion molecules, and fragments of antibodies and radiolabeled interleukin This discussion also includes 99m Tc-labeled ciprofloxacin and other labeled antibiotics as imaging agents. The last chapter involved the labeling of microorganisms and parts of microorganisms, but the writing is, unfortunately, somewhat choppy and less clear.


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Overall, I very much recommend this book as a worthwhile reference for any nuclear medicine professional dealing with infectious or tropical diseases. The book does, however, have some limitations. The quality of the images is poor, but whether because of poor reproduction by the publisher or poor source images is hard to tell. However, the images do carry the message. Another concern about the book is that it has practically no correlative images. As far as I could see, the only nonnuclear image in the whole book is one CT scan of the brain.

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It would have been helpful if the authors had presented some correlative imaging by CT, MRI, or sonography—specifically, where these other images failed and nuclear medicine excelled or was more specific in a particular case. This book was, however, published in , and perhaps a new edition will soon become available with better-quality images and more correlative images. Nevertheless, I meanwhile recommend acquisition of this current edition.

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Division of Infectious Disease & Tropical Pediatrics | University of Maryland School of Medicine

Primary outcome [1] 0. Primary Outcome 1: Intra-individual PET tracer uptake changes in regions of interest post malaria inoculation prospective regions of interest include: spleen, bone marrow, brian and skeletal muscle. Timepoint [1] 0. Primary outcome 1 Timepoint: baseline and estimated days following low dose malaria inoculation. Primary outcome [2] 0.

Primary Outcome 2: Intra-individual MRI imaging changes in regions of interest post malaria inoculation prospective regions of interest include: spleen, bone marrow, brian and skeletal muscle. Timepoint [2] 0. Primary outcome 2 Timepoint: baseline and estimated days following low dose malaria inoculation. Secondary outcome [1] 0. Secondary Outcome 3: The impact of early malaria infection on glucose metabolism will be evaluated based on the the biodistribution and degree of uptake of the PET tracer.


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  • Secondary Outcome 3 Timepoint: estimated days following low dose malaria inoculation. Key inclusion criteria. Minimum age. Maximum age. Males Query! Can healthy volunteers participate? Yes Query! Key exclusion criteria. Any nuclear medicine imaging e. Greater than one previous CT scan c. Note: previous plain film X-rays and mammography are acceptable Query!

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    Natural history Query! Longitudinal Query! Defined population Query! Prospective Query! The population will comprise of approximately eight adult participants. This population size has been estimated based on the clinical experience of the subinvestigators. It is expected that this study will be hypothesis generating. Recruitment status. Completed Query! Date of first participant enrolment. Date of last participant enrolment. Date of last data collection. Sample size.

    Recruitment in Australia. Recruitment state s. QLD Query! Recruitment postcode s [1] 0.