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David W. Johnson

Researcher at University of Queensland

Publications -  2880
Citations -  157072

David W. Johnson is an academic researcher from University of Queensland. The author has contributed to research in topics: Peritoneal dialysis & Kidney disease. The author has an hindex of 160, co-authored 2714 publications receiving 140778 citations. Previous affiliations of David W. Johnson include Minnesota Department of Transportation & Open University.

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Speciation of arsenic metabolites in the urine of occupational workers and experimental rats using an optimised hydride cold-trapping method†

TL;DR: A hydride cold-trapping technique was developed and optimised for the measurement of urinary arsenic metabolites and up to two fold increases of urinary ASi excretion in rats compared with control rats were also observed in animals dosed with various forms of arsenicals.
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Improved risk stratification in myeloma using a microRNA-based classifier.

TL;DR: This is the first report showing that miRNAs can be built into molecular diagnostic strategies for risk stratification in MM, and an “outcome classifier”, based on the expression of two mi RNAs, which is able to stratify patients into three risk groups.
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How Safe Are Common Analgesics for the Treatment of Acute Pain for Children? A Systematic Review.

TL;DR: Evidence comparing the safety profiles of three groups of oral medications, acetaminophen, nonsteroidal anti-inflammatory drugs, and opioids, to manage acute nonsurgical pain in children treated in ambulatory settings highlights challenges in assessing medication safety, including lack of more detailed information in registry data, and inconsistent reporting in trials.
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A Randomized Trial on the Effect of Phosphate Reduction on Vascular End Points in CKD (IMPROVE-CKD).

TL;DR: In patients with stage 3b/4 CKD, treatment with lanthanum over 96 weeks did not affect arterial stiffness or aortic calcification compared with placebo, and the role of intestinal phosphate binders to reduce cardiovascular risk in patients with CKD who have normophosphatemia is not supported.
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A comparative study of straight chain and branched chain fatty acid oxidation in skin fibroblasts from patients with peroxisomal disorders.

TL;DR: The data presented indicate that the oxidation of alpha- and gamma-methyl isoprenoid-derived fatty acids takes place largely in peroxisomes in human skin fibroblasts.