Results 201 to 210 of about 45,897 (233)
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Lyophilized Human Dura Mater as a Dural Substitute
Journal of Neurosurgery, 1958P C, SHARKEY +3 more
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Clinical Use of Freeze-Dried Human Dura Mater
Journal of Neurosurgery, 1958J B, CAMPBELL +2 more
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Duraplasty with pretreated freeze-dried sterilized human dura mater.
Sbornik vedeckych praci Lekarske fakulty Karlovy university v Hradci Kralove, 1991Different collagenic tissues, such as allogeneic fascia lata, dura mater and xenogeneic pericardium preserved by deep freezing or freeze-drying and packed in National Blood Service jars have been used with good clinical results in duraplasties performed at the Department of Neurosurgery, University Hospital at Hradec Králové since 1956.
J, Parízek, P, Mĕricka
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Antigenic properties of fresh and lyophylised human dura mater.
Journal of neurosurgical sciences, 1988The action of human fresh and lyophylised human dura mater on rat, rabbit and human serum complement has been analyzed with the aim of confirming and comparing the species-specific antigenicity of both substances. The results demonstrate that both fresh and lyophylised human dura mater induce a complement consumption on rat and rabbit serum.
OCCHIOGROSSO M +2 more
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A biomimetic triple-layered biocomposite with effective multifunction for dura repair
Acta Biomaterialia, 2021Xiaoming Li, Wei He, Qi Guo
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Dural defektlerin onarımında dehidrate human Dura mater`in kullanımı
202042 SUMMARY This study was conducted on 60 white male hybrid rabbits whose weights are 2.5-3.5 kg. The rabbits were divided into two groups as a study group and a control group. The rabbits in both groups anesthetized with Ketalar a dural defect of 1x1 cm in size was created on the left parietal area via craniectomy, in the study group the dehydrated ...
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A review of cancer immunotherapy toxicity
Ca-A Cancer Journal for Clinicians, 2020Lucy Boyce Kennedy
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Neurological devices; classification of human dura mater. Final rule.
Federal register, 2004The Food and Drug Administration (FDA) is classifying human dura mater intended to repair defects in human dura mater into class II (special controls). This action is being taken to establish sufficient regulatory control to provide reasonable assurance of the safety and effectiveness of the device.
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