Use the labels in the right column to find what you want. Or you can go thru them one by one, there are only 29,294 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.
Lung stem/progenitor cells are
potentially useful for regenerative therapy, for example in repairing
damaged or lost lung tissue in patients. Several optical imaging methods
and probes have been used to track how stem cells incorporate and
regenerate themselves in vivo over time. However, these
approaches are limited by photobleaching, toxicity and interference from
background tissue autofluorescence. Here we show that fluorescent
nanodiamonds, in combination with fluorescence-activated cell sorting,
fluorescence lifetime imaging microscopy and immunostaining, can
identify transplanted CD45–CD54+CD157+ lung stem/progenitor cells in vivo,
and track their engraftment and regenerative capabilities with
single-cell resolution. Fluorescent nanodiamond labelling did not
eliminate the cells’ properties of self-renewal and differentiation into
type I and type II pneumocytes. Time-gated fluorescence imaging of
tissue sections of naphthalene-injured mice indicates that the
fluorescent nanodiamond-labelled lung stem/progenitor cells preferentially reside at terminal bronchioles of the lungs for 7 days after intravenous transplantation.
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