Home - Neuromuscular Disease Foundation

Stay up to date - subscribe to our newsletter. AWARENESS. SCREENING. CURE. HIBM also known as GNE Myopathy is a rare and debilitating form of muscular dystrophy that causes muscles to waste away and robs people of their ability to do all of the everyday activities that the rest of us take for granted. While the recessive form of the disease is most common among Jews, Persians and the Japanese community, HIBM affects people around the world. There is currently no treatment or cure. Space is Limited .

OVERVIEW

This web site ndf-hibm.org presently has an average traffic ranking of zero (the smaller the better). We have probed nine pages inside the web site ndf-hibm.org and found twenty-nine websites associating themselves with ndf-hibm.org. There is two contacts and addresses for ndf-hibm.org to help you correspond with them. There is one social networking accounts acquired by this website. This web site ndf-hibm.org has been online for nine hundred and eight weeks, thirty days, nine hours, and twenty-four minutes.
Pages Analyzed
9
Links to this site
29
Contacts
2
Locations
2
Social Links
1
Online Since
Sep 2007

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NDF-HIBM.ORG HISTORY

This web site ndf-hibm.org was first documented on September 20, 2007. It is now nine hundred and eight weeks, thirty days, nine hours, and twenty-four minutes old.
REGISTERED
September
2007

MATURITY

17
YEARS
4
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LINKS TO WEB PAGE

GeneTestNow! The number 1 source for Jewish Genetic Disease Information Put the odds on your side

Put the odds on your side! 1 in 4 Jews is a carrier for a common preventable deadly disease. Take the first step toward prevention and get screened! Straight Talk about Genetic Testing. Learn more about how to prevent some of the diseases. An open letter to the Jewish community from your local rabbis on the importance of genetic testing. Click here to download our FREE brochure.

Home Jain Foundation

Free Genetic Diagnosis for LGMDs. Free diagnosis tool for physicians. The Jain Foundation has cultivated a robust dysferlin research field that spans the globe.

Living With HIBM What its like to live with a progressive neuromuscular disease

Then the upper body weakness set in. It had actually been there all along, but not in the significant, disabling way it was slowly morphing into. How foolish I had been for believing that not being able to walk was the most dreaded outcome of this disease. There is an easy fix for that disability. Such is not the case for hand, arm, upper back and shoulder weakness. Resolve to Get Naked in 2018.

Rare Genetic Diseases Ultragenyx

Deep and diversified product pipeline. Developing multiple clinical-stage programs in parallel. Focused on serious rare and ultra-rare diseases. Working with patients and medical professionals to treat rare diseases. Dedicated to creating new treatments. Join a high-performance team focused on rare diseases. Ultragenyx Reports Second Quarter 2015 Financial Results and Corporate Update.

Tara Talks GNE Myopathy

I will invite others to share their stories, tips, and comments. I will also discuss potential treatments, clinical trials, current research, and ways of supporting each other on this interesting and challenging journey. Friday, December 30, 2016.

Living with HIBM

Sunday, August 10, 2014. Sunday, June 1, 2014. It just so happens that last night was such an incredible gift. How am I to cope? .

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CONTACTS

NEUROMUSCULAR DISEASE FOUNDATION

269 SOUTH BEVERLY DRIVE

BEVERLY HILLS, California, 90212

US

Reginet.com Domains for 9.99

11323 Idaho Ave

Los Angeles, California, 90025

US

NDF-HIBM.ORG HOST

Our web crawlers revealed that a lone page on ndf-hibm.org took zero milliseconds to stream. Our crawlers could not detect a SSL certificate, so therefore our web crawlers consider this site not secure.
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0 seconds
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NOT SECURE
Internet Address
74.220.207.119

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ns1.hostmonster.com
ns2.hostmonster.com

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SERVER OPERATING SYSTEM AND ENCODING

I revealed that ndf-hibm.org is employing the Apache server.

PAGE TITLE

Home - Neuromuscular Disease Foundation

DESCRIPTION

Stay up to date - subscribe to our newsletter. AWARENESS. SCREENING. CURE. HIBM also known as GNE Myopathy is a rare and debilitating form of muscular dystrophy that causes muscles to waste away and robs people of their ability to do all of the everyday activities that the rest of us take for granted. While the recessive form of the disease is most common among Jews, Persians and the Japanese community, HIBM affects people around the world. There is currently no treatment or cure. Space is Limited .

CONTENT

This web site states the following, "Stay up to date - subscribe to our newsletter." Our analyzers noticed that the web site also said " HIBM also known as GNE Myopathy is a rare and debilitating form of muscular dystrophy that causes muscles to waste away and robs people of their ability to do all of the everyday activities that the rest of us take for granted." The Website also said " While the recessive form of the disease is most common among Jews, Persians and the Japanese community, HIBM affects people around the world. There is currently no treatment or cure."

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