Yesterday the US Food and Drug Administration (FDA) announced a Class I recall for the low-profile, thin-walled peripheral guiding sheath known as Halo One. Device manufacturer Bard Peripheral ...
Please provide your email address to receive an email when new articles are posted on . The FDA has designated a recall of a sheath used to introduce and/or guide the placement of interventional and ...
In the current study, we evaluated the potential role of H3K27me3 immunohistochemical expression in daily routine practice to distinguish malignant peripheral nerve sheath tumor from its main ...
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