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Previous studies focused on incentivizing one group or the other have produced only moderate improvements for patients, but when we look at it as a twoway street where patients and physicians each bear responsibility, the findings then become consistent with what we might intuitively expect.

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But their point is legitimate, as openaccess journals remove the profit motive from deciding which studies to publish, which creates a motivation to publish positive studies that will garner readers, media attention, and requests for reprints.

IRB posts their per FDA rules. I encourage you to take a look.

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Greece and Italy are the largest users of biosimilar filgrastims.

DEG was at this point known to be toxic, although the exact extent of its toxicity was not known.

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The amount of premarket and postmarket immunogenicity data needed for a potential biosimilar will depend on an analytical assessment of similarity between the biosimilar and its reference product, as well as the rate of clinical consequences of immunogenicity observed with the reference product.

Hospitalacquired infections are the most common complication of hospital care in the United States and result in extended hospital stays, higher costs and increased risk of patient death.

In test tubes these antibodies stopped cocaine in its tracks, and when the vaccine was injected into mice before cocaine exposure, the animals displayed much less hyperactivity when given cocaine even in large, repeated doses than nonvaccinated mice.

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Funding was provided by the Quirk family of Calgary, by the HBI, and the Clinical Research Unit at UCalgary.

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There about changes in behavior and psychological wellbeing following false positives.

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Cargill says its possible that in the future, this list of genes that are uniquely human may provide researchers with a better target for researching genes that cause human disease.

Iron-Refractory Microcytic Anemia as the Presenting Feature of Unicentric Castleman Disease in Children.

The treatment regimen was generally associated with low-intensity-type toxicities, and so it is also considered to be low intensity therapy.

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The importance of accurate and timely diagnosis and intervention in this condition should be recognized and emphasized by pharmacists.

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If reference products are therapeutic counterparts of endogenous proteins with crucial, non-redundant, biological functions, or are known to provoke anaphylaxis, detailed immunogenicity studies will be required.

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