Hello all, :) Hope you're doing well. Someone asked me about the decrypton, so I thought you might be interested too. This is my 2 cents about it: In France...
There are 8 presentations and one discussion workshop on dysferlin in the program for the upcoming Internatioal Congress on Neuromuscular Diseases in July...
I've decided to activate the "moderater" feature on posting messages. Most people recieve all the postings as e-mails (you can change this under the options...
Thanks, Brad. I think we do need you stepping in. Not that I get all that much mail from the group, but it's a bother when it's a repeat or a spam attack. ...
... Daniel: Thanks for the mention, Brad! While I won't be able to attend the Congress myself, several people from my lab will be paying close attention to the...
Dear members, Since the dysferlin gene is known, why antisense/sense paradigm has not been used more intensively in clinical research? Ce paradigm is based on...
... Dear Sophareth, Thanks for answering and furthering my questions in a so unexpected way, though. I was thinking that antisense/ sense RNA paradigm's...
Dear Dyferliners, Dysferlinopathies seem to be, at least for instant, a recessive disorder. Such as the antisense/sense paradigm (suppression of pathological...
Nat, The big big problem is to define precisely the molecular etiology of diverse forms of dysferlinopathies and their numberless regulation networks. ...
Dear dysferliners, I've posted in the group bookmark a few links which might interested some of you about MD infos. One of them is the URL of the dysferlin...
Dear sophareth and all, Ok, to avoid all confusion, you can call me Nat all ( shorter, et cuter than Phalevi, duh?) Just checked the scheme in the photos...
I'm posting this message for natalisan, who is currently having internet connection trouble :-( The decrypthon acts as a sort of screen saver, to have your...
A friend of mine, Ricardo Rojas, has proposed establishing Sept. 17 (the birthday of Dr. Guillaume Duchenne, who gave the first clinical description of the...
Hi everyone! Nice to be back! Thank you Brad for filling in my last message for me:) Concerning RNA interference/ repairing. An intro to this new kind of...
I was wondering if anyone in this group knows any information about current diagnostic tests available for LGMD type 2B. I've read that there are a number of...
Hi Lucinda, The diagnostic test currently done involves testing for the presence of the dysferlin protein, using an antibody which recognizes dysferlin....
Thanks Brad for the very helpful information on diagnostic testing. I've been wondering if anyone in this group has had a similar experience of rate of...
Hello All My name is Aman and I have had a similar experience. In high school, I had elevated liver enzymes but no symptoms. I weightlifted, ran track, and...
Hello, I just found out that a member of our family is diagnosed with Miyoshi Myopathy. How can I help? __________________________________________________ Do...
Hello all (esp. Lucinda), Because of recent efforts to get a DNA analysis of my dyferlin genes--not to had currently, unless anyone knows otherwise (if so, ...
Hi everyone, An article has just appeared in the scientific journal Nature which reports some very interesting results on the dysferlin protein. The ...
Hi everyone. I am glad to find this group, and I look forward to swapping thoughts, questions, info back and forth. The main thing I want to address is rate of...
Hi yall, Children's Hospital in DC, which has a large and reputable research center, is going to be studying DNA sequence/mutations in the dysferlin gene. I'm...
Hello everybody, I'm so relieved to find a newsgroup dealing with dysferlin deficiency. I'm very interested in what others are going through. Thank you Brad,...
Amanda. My name is Mathew and I havent introduce myself to the group yet.I am a resident of Ontario, and I have been diagnosed (sort of...) with Myoshi...
Hello Amanda, I actually was diagnosed with LGMD 2B a couple of years ago as well. At first, Doctors told me that I had Polymyositis but I did not respond to...
Hello! I haven't posted in over a year, but I do try to check in regularly. I guess there aren't many of us out there so this group is destined to move very...
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