Matt O'Connor on Muck Rack

Matt O'Connor

Glen Ellyn
As seen in: Wiley Online Library, BMJ Open, Chicago Tribune, Entrepreneur, Fast Company, Business 2 Community, New Milford Spectrum, AIThority, Health Imaging, HealthExec and
Longtime former Chicago Tribune reporter/editor still figuring out his next chapter. Proud father and grandfather.
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Articles

Developing Effective Flow Enhancement Strategies for Salmonid Recovery and Climate Change Adaptation in Central California's Coastal Watersheds

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By Matt O'Connor, Mariska Obedzinski, Jeremy Kobor
| Wiley Online Library
References , , , and . 1988. “Guidelines for Computing Crop Water Requirements.” Irrigation and Drainage Paper 56. , , and . 2002. “United States Geological Survey Miscellaneous Field Studies Map MF-2402.” , , , , , and . 2013. “Determining Appropriate Instream Flows for Anadromous Fish Passage on an Intermittent Mainstem River, Coastal Southern California, USA.” Ecohydrology 7: 745–759. California Department of Fish and Game (CDFG). 2004.
Open in Who Shared Issue with article?
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By Matt O'Connor
| Health Imaging
Readouts are essential for educating radiologists-in-training, yet few providers truly understand how much this practice influences young readers. Training programs must begin having such discussions, particularly as interpretations move out of the reading room and soon-to-be rads are forced to learn from their own homes. That was the argument made by two radiologists from the University of Maryland School of Medicine, in Baltimore, in a new editorial published by RadioGraphics.
Open in Who Shared Issue with article?

‘A major regulatory win’: Imaging advocates praise new rule enhancing coverage for breakthrough devices

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By Matt O'Connor
| Health Imaging
The Medical Imaging & Technology Alliance on Thursday praised a recently issued final rule that will eliminate regulatory red tape slowing coverage of innovative imaging devices and other medical technologies. Finalized Monday by the Centers for Medicare & Medicaid Services, this rule creates a new pathway to expedite patient access to “breakthrough” devices, as deemed by the U.S. Food & Drug Administration.
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