VoiceBrook is an awesome pathology voice recognition system! We use Meditech
and it does not require an interface.
Michelle
From: Ann Specian thisis...@aol.com
To: histonet@lists.utsouthwestern.edu
Sent: Tuesday, January 15, 2013 6:37 PM
Subject: [Histonet]
As an LIS vendor I hear this question quite often. I'd like to make an
attempt to address this query for the benefit of the group.
To start with, if your APLIS uses a version of Microsoft WORD to enter
gross, or any other part of the report for that matter, then Dragon should
work pretty much
We use Dragon for micro. We found the gross room took more time editing than
transcribing, so we gave up on using it there.
Joyce Weems
Pathology Manager
678-843-7376 Phone
678-843-7831 Fax
joyce.we...@emoryhealthcare.org
www.saintjosephsatlanta.org
5665 Peachtree Dunwoody Road
Atlanta, GA
It is polymer. No endogenous biotin-problem.
The staining looks quiet specific. It is confined to cytoplasm. And there are
clear negativ cells beside faintly stained positiv cells.
I'm reading about the envading features of helicobacter into host cells and
about the injection of VacA and CagA
Have you checked to see if patient treatment might be a factor?
Joyce Weems
Pathology Manager
678-843-7376 Phone
678-843-7831 Fax
joyce.we...@emoryhealthcare.org
www.saintjosephsatlanta.org
5665 Peachtree Dunwoody Road
Atlanta, GA 30342
This e-mail, including any attachments is the property
I quite often see faint cytoplasmic staining in immunostains for
Helicobacter. You're supposed to ignore it. It's often present in the
negative control slide - one of the few reasons I ever look at a
negative control slide.
These days I get my IHC for Helicobacter from whatever Genzyme is
called
A time-lapse movie showing the immune response in the lymph nodes of a
mouse edged out a fruit fly sperm fight for top honors at this year's
Nikon Small World in Motion Photomicrography competition.
http://www.scientificamerican.com/video.cfm?id=art-and-science-come-together-in-ni2013-01-15
Hello to the eye experts,
I am currently working on a large animal (LA) eye project which will
give me the flexibility of experimenting with different fixatives.
I am currently using Modified Davidson's solution (48 hours) followed by
a 10% NBF solution prior to trimming the eyes, embedding ,
I'm curious about this as well.
We work with mice and rats in our lab and whenever we need eyes (corneas,
more specifically), we immersion fix them whole in Bouin's solution
overnight at 4C then transfer to 70% EtOH until we're ready to excise the
corneas, process and embed into paraffin. We've
We work with mice and do a variety of fixatives, but we prefer a
methanol/acetic acid fixative. It holds the shape of the eye very well,
although it may not show the Schlemm's canal as well as other fixatives.
-Liz
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From: histonet-boun...@lists.utsouthwestern.edu
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