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10.2217/fnl.14.44

http://scihub22266oqcxt.onion/10.2217/fnl.14.44
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C4266275!4266275!25530721
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suck abstract from ncbi


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pmid25530721      Future+Neurol 2014 ; 9 (5): 541-51
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  • Animal models of stroke: translational potential at present and in 2050 #MMPMID25530721
  • Herson PS; Traystman RJ
  • Future Neurol 2014[Sep]; 9 (5): 541-51 PMID25530721show ga
  • Translation from basic science bench research in ischemic stroke to bedside treatment of patients suffering ischemic stroke remains a difficult challenge. Despite literally hundreds of compounds and interventions that provide benefit in experimental models of cerebral ischemia, efficacy in humans remains to be demonstrated. The reasons for failure to translate the extensive positive basic science findings to successful clinical trials have been the focus of discussion for years. Some attribute the failure to flaws in clinical trial design, others question the predictive value of current animal models and some question the quality of preclinical data. It is likely that a combination of all these shortcomings have ultimately led to the failure. The purpose of this review is to analyze the commonly used animal models used in the field today, provide a framework for understanding the current state of basic science research in the ischemic stroke field and discuss a path forward.
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