Use the labels in the right column to find what you want. Or you can go thru them one by one, there are only 27,7563 posts. Searching is done in the search box in upper left corner. I blog on anything to do with stroke.DO NOT DO ANYTHING SUGGESTED HERE AS I AM NOT MEDICALLY TRAINED, YOUR DOCTOR IS, LISTEN TO THEM. BUT I BET THEY DON'T KNOW HOW TO GET YOU 100% RECOVERED. I DON'T EITHER, BUT HAVE PLENTY OF QUESTIONS FOR YOUR DOCTOR TO ANSWER.
Changing stroke rehab and research worldwide now.Time is Brain!trillions and trillions of neuronsthatDIEeach day because there areNOeffective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.
What this blog is for:
My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.
Saturday, October 10, 2015
Three-dimensional macroporous nanoelectronic networks as minimally invasive brain probes
This seems like it would be very useful for our stroke researchers to listen in on neurons talking to each other. Then we could maybe find out exactly how neuroplasticity works. Why would a neuron give up its' current task to help out a neighboring neuron? How is that accomplished? Without knowing these answers neuroplasticity is not consistently repeatable. Which means that none of the research into neuroplasticity is valid right now.
The other possibilities for listening in on the brain:
Direct electrical recording and stimulation of neural
activity using micro-fabricated silicon and metal micro-wire probes have
contributed extensively to basic neuroscience and therapeutic
applications; however, the dimensional and mechanical mismatch of these
probes with the brain tissue limits their stability in chronic implants
and decreases the neuron–device contact. Here, we demonstrate the
realization of a three-dimensional macroporous nanoelectronic brain
probe that combines ultra-flexibility and subcellular feature sizes to
overcome these limitations. Built-in strains controlling the local
geometry of the macroporous devices are designed to optimize the
neuron/probe interface and to promote integration with the brain tissue
while introducing minimal mechanical perturbation. The ultra-flexible
probes were implanted frozen into rodent brains and used to record
multiplexed local field potentials and single-unit action potentials
from the somatosensory cortex. Significantly, histology analysis
revealed filling-in of neural tissue through the macroporous network and
attractive neuron–probe interactions, consistent with long-term
biocompatibility of the device.
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