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Messages 75 - 104 of 331   Oldest  |  < Older  |  Newer >  |  Newest
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75
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...
sophareth
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Jul 17, 2002
11:35 pm
76
I'm quite agree with this right initiative. Sophareth ... messages. ... this ... to ... doing...
sophareth
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Jul 21, 2002
4:59 pm
77
... Dear Sophareth, Thanks for answering and furthering my questions in a so unexpected way, though. I was thinking that antisense/ sense RNA paradigm's...
natalisan
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Jul 21, 2002
4:59 pm
78
Dear Dyferliners, Dysferlinopathies seem to be, at least for instant, a recessive disorder. Such as the antisense/sense paradigm (suppression of pathological...
sophareth
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Jul 21, 2002
4:59 pm
79
This image is a complement to my last letter 18 july on RNA-mediated repair of gene instruction. sophareth sophareth <sophareth@...> a écrit : Dear...
sophareth Camsonne
sophareth
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Jul 21, 2002
4:59 pm
80
Nat, The big big problem is to define precisely the molecular etiology of diverse forms of dysferlinopathies and their numberless regulation networks. ...
sophareth Camsonne
sophareth
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Jul 28, 2002
9:38 pm
81
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...
natalisan
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Aug 27, 2002
2:56 am
82
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...
natalisan
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Aug 27, 2002
2:56 am
83
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...
baw1064
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Sep 17, 2002
2:06 am
84
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...
baw1064
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Sep 17, 2002
2:06 am
85
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...
natalisan
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Sep 24, 2002
1:31 am
86
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...
lucinda_hodges
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Mar 30, 2003
7:08 pm
87
Hi Lucinda, The diagnostic test currently done involves testing for the presence of the dysferlin protein, using an antibody which recognizes dysferlin....
baw1064
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Mar 30, 2003
7:24 pm
88
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...
lucinda_hodges
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Mar 31, 2003
5:31 am
89
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...
Aman
kingpin3dd
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Mar 31, 2003
11:14 pm
90
Hello, I just found out that a member of our family is diagnosed with Miyoshi Myopathy. How can I help? __________________________________________________ Do...
Mohamed Ali
sixalis
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Apr 2, 2003
1:41 am
91
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, ...
Ryan,Marian
cody0492
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Apr 2, 2003
1:42 am
92
Hi everyone, An article has just appeared in the scientific journal Nature which reports some very interesting results on the dysferlin protein. The ...
baw1064
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May 8, 2003
12:37 am
93
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...
Lary Lumpkin
lary_lump
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May 23, 2003
11:17 pm
94
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...
Ryan,Marian
cody0492
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Jun 19, 2003
10:28 pm
95
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,...
inquisitivemind3
inquisitivem...
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Aug 23, 2003
1:20 am
96
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...
fregos
vlacas2002
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Aug 23, 2003
3:04 am
97
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...
Aman
kingpin3dd
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Aug 23, 2003
10:41 pm
98
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...
fretmaster6
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Aug 23, 2003
10:42 pm
99
Hi, welcome to the group:) Kendra Carter-Hurte Baltimore, MD...
khurte@...
khurte
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Aug 25, 2003
11:19 pm
100
Hello, I just wanted to thank everybody who responded to my email posted in August. I may have been very slow to reply, but I greatly appreciated everybody's...
inquisitivemind3
inquisitivem...
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Sep 28, 2003
7:47 pm
101
Hi I'm Suzanne, from England, & I've been diagnosed with Miyoshi Distal Myopathy. I have a very suppotive husband, a son of four years old and a one year old...
Suzanne Croft
craftycroftyuk
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Oct 2, 2003
1:20 am
102
Hi friends Do you have any update on this question about how to detect the dysferlin in the blood? I have a nephew that had a problem of MD and we are trying...
Raul
rolivera
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Oct 15, 2003
1:15 am
103
Hi , I'm looking for others in my general age group (I'm 49 ) that have LGMD 2B, live alone, and would like someone to correspond with. My email is...
cadiame
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Apr 25, 2004
8:30 pm
104
Hi I'm Kendra, I'm 32 years old. I live with my husband of 6 1/2 years and two children. We can chat if you like. Wishing you Love, Peace & Happiness Kendra...
khurte@...
khurte
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Apr 25, 2004
8:43 pm
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