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Titlebook: Brain Injury; Robert S. B. Clark,Patrick Kochanek Book 2001 Springer Science+Business Media New York 2001 Alzheimer.Neurointensiv.Trauma.a

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發(fā)表于 2025-3-21 19:19:02 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Brain Injury
影響因子2023Robert S. B. Clark,Patrick Kochanek
視頻videohttp://file.papertrans.cn/191/190203/190203.mp4
學(xué)科分類Molecular & Cellular Biology of Critical Care Medicine
圖書封面Titlebook: Brain Injury;  Robert S. B. Clark,Patrick Kochanek Book 2001 Springer Science+Business Media New York 2001 Alzheimer.Neurointensiv.Trauma.a
影響因子.Brain Injury. is the second volume in the book series,Molecular and Cellular Biology of Critical Care Medicine. In thisvolume, a group of internationally regarded experts in important areasof neuroscience and neurointensive care research address the molecularand cellular basis of acute brain injury. .This text covers acute brain injury within a context relevant to thecare of patients with critical neurologic injuries such as cardiacarrest, trauma and stroke. It includes recent data pertaining toestablished pathways such as neurotransmission, exitotoxicity,ionic-mechanisms, oxidative stress, inflammation, and cerebralvascular injury. In addition, rapidly developing areas such as cellsignaling, adenosine pharmacology, apoptosis, mitochondrialdysfunction, neurocytoskeletal changes, and the role of trophicfactors are reviewed from the level of in vitro modeling to humandata. Other topics covered that are highly clinically relevant includethe effect of genetic background and gender differences in outcomeafter brain injury, preconditioning, and the effects of currently usedanesthetics and sedative agents in patients with brain injury.
Pindex Book 2001
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書目名稱Brain Injury影響因子(影響力)




書目名稱Brain Injury影響因子(影響力)學(xué)科排名




書目名稱Brain Injury網(wǎng)絡(luò)公開度




書目名稱Brain Injury網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Brain Injury被引頻次




書目名稱Brain Injury被引頻次學(xué)科排名




書目名稱Brain Injury年度引用




書目名稱Brain Injury年度引用學(xué)科排名




書目名稱Brain Injury讀者反饋




書目名稱Brain Injury讀者反饋學(xué)科排名




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發(fā)表于 2025-3-21 20:14:50 | 只看該作者
openSAP – der Enterprise-MOOC-Pioniersent novel targets for therapies aimed at limiting damage after acute or chronic CNS injury. This chapter will provide a general review of death receptors and their signaling mechanisms, focusing on the two best characterized death receptors, Fas and TNF-α.
板凳
發(fā)表于 2025-3-22 01:57:39 | 只看該作者
Machen elektromagnetische Felder krank?l disintegration, nuclear condensation, and digestion of DNA. Finally, the engulfment of the dead cell or cell fragments by phagocytosis peacefully terminates the death program. Incomplete execution of programmed cell death may redirect the cell to necrosis, which is an unfavorable event for the org
地板
發(fā)表于 2025-3-22 05:35:45 | 只看該作者
Machiavelli in Contemporary Media neurocytoskeletal elements sustain damage as a result of trauma, potentially contributing to neuronal dysfunction. Some of the major neurocytoskeletal proteins include neurofilaments (NFs), tubulin, microtubule-associated proteins (MAPs) such as MAP2 and tau, actin, and spectrin. Because cytoskelet
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發(fā)表于 2025-3-22 09:35:45 | 只看該作者
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發(fā)表于 2025-3-22 13:51:37 | 只看該作者
The Multifaceted Role of Adenosine in Experimental and Clinical Traumatic Brain Injury,thermia—putative pharmacological agents that might simultaneously or sequentially confer multiple beneficial effects in the injured brain. One endogenous mediator that fits this category is adenosine—which has the potential to favorably influence excitotoxicity, energy failure, hypoperfusion, calciu
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發(fā)表于 2025-3-22 18:10:03 | 只看該作者
Death Receptors in Acute Brain Injury,sent novel targets for therapies aimed at limiting damage after acute or chronic CNS injury. This chapter will provide a general review of death receptors and their signaling mechanisms, focusing on the two best characterized death receptors, Fas and TNF-α.
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發(fā)表于 2025-3-22 22:51:06 | 只看該作者
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發(fā)表于 2025-3-23 03:50:13 | 只看該作者
Neurocytoskeletal Changes Following Traumatic Brain Injury, neurocytoskeletal elements sustain damage as a result of trauma, potentially contributing to neuronal dysfunction. Some of the major neurocytoskeletal proteins include neurofilaments (NFs), tubulin, microtubule-associated proteins (MAPs) such as MAP2 and tau, actin, and spectrin. Because cytoskelet
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發(fā)表于 2025-3-23 07:10:15 | 只看該作者
Reproductive Hormones as Neuroprotectants in Brain Injury,d molecular mechanisms by which estrogen salvages brain are detailed. We focus on estrogen’s mechanisms since there is a large, and rapidly developing, understanding of this hormone’s neuroprotective potential. Limited data are available at present for progesterone or testosterone (reviewed in .; .)
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