Rare Diseases Clinical Research Network - YOU Can Contribute to Rare Diseases Research and Treatment!

Finding new approaches to diagnosis, prevention, and treatment of rare diseases and disorders - The National Institutes of Health Rare Diseases Clinical Research Network RDCRN was created to facilitate collaboration among patients and experts in many different types of rare diseases.

OVERVIEW

The site rarediseasesnetwork.org presently has a traffic ranking of six hundred and forty-three thousand nine hundred and eleven (the lower the more traffic). We have downloaded twenty pages within the web page rarediseasesnetwork.org and found one hundred and thirty-one websites referencing rarediseasesnetwork.org. We have noted one contacts and addresses for rarediseasesnetwork.org to help you contact them. The site rarediseasesnetwork.org has been online for one thousand and seventy-two weeks, nineteen days, three hours, and nineteen minutes.
Traffic Rank
#643911
Pages Parsed
20
Links to this site
131
Contacts
1
Addresses
1
Online Since
Oct 2003

RAREDISEASESNETWORK.ORG TRAFFIC

The site rarediseasesnetwork.org is seeing varying quantities of traffic all through the year. Chiefly, the web page had a ranking today of six hundred and forty-three thousand nine hundred and eleven.
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RAREDISEASESNETWORK.ORG HISTORY

The site rarediseasesnetwork.org was first recorded on October 07, 2003. It is currently one thousand and seventy-two weeks, nineteen days, three hours, and nineteen minutes old.
REGISTERED
October
2003

SITE LENGTH OF LIFE

20
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LINKS TO RAREDISEASESNETWORK.ORG

Welcome APS Foundation of America, Inc

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Churg Strauss Syndrome - Vasculitis - Support and Assistance for Churg Strauss - Autoimmune Disease - Inflammation of Blood Vessels - Churg Strauss Syndrome - Vasculitis - Pub Med -

Join our list of donors and. Make a difference today! The Churg-Strauss Syndrome Association Supports and Empowers Patients Through Education, Awareness and Research. Vasculitis Foundation Chapters and Support Groups. What is Churg Strauss Syndrome. Vasculitis Foundation Funds Two EGPA Research Projects. These studies were made possible by a very generous gift from an EGPA family. New Research Article on ENT Involvement in EGPA.

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Official List of Lysosomal Diseases. Official List of Lysosomal Diseases. 2018 Rare Disease Day at NIH. Event Video is Now Available. And the NIH Clinical Center.

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Osteogenesis Imperfecta Foundation OIF.org

Books, Brochures and Fact Sheets. Community Resources and Impact Grant Program. Audio and Video Learning Center. Brittle Bone Disorders Rare Disease Consortium. 50,000 Lives, One Unbreakable Spirit. 50,000 Laps, One Unbreakable Spirit. Blue Jeans for Better Bones. What is Osteogenesis Imperfecta? The Osteogenesis Imperfecta Foundation.

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CONTACTS

USF - HII

DNS Admin

3650 Spectrum Blvd

Tampa, Florida, 33620

US

RAREDISEASESNETWORK.ORG SERVER

We diagnosed that the main page on rarediseasesnetwork.org took one hundred and eighty-one milliseconds to load. I could not observe a SSL certificate, so our parsers consider rarediseasesnetwork.org not secure.
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0.181 sec
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NOT SECURE
IP
131.247.54.80

NAME SERVERS

mother.usf.edu
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FAVICON

SERVER SOFTWARE

We discovered that this domain is implementing the Microsoft-IIS/7.5 server.

SITE TITLE

Rare Diseases Clinical Research Network - YOU Can Contribute to Rare Diseases Research and Treatment!

DESCRIPTION

Finding new approaches to diagnosis, prevention, and treatment of rare diseases and disorders - The National Institutes of Health Rare Diseases Clinical Research Network RDCRN was created to facilitate collaboration among patients and experts in many different types of rare diseases.

PARSED CONTENT

The site had the following on the web site, "Are YOU Interested in Research on Rare Diseases? Have study information sent right to your inbox! Receive the most current information on." I observed that the web page said " Open recruitment for clinical studies of your disease." They also stated " Opening of new clinical sites doing research on rare diseases. Activities from affiliated awareness and advocacy groups. And future opportunities to participate in research! YOU can help in the fight against rare diseases. Improve methods in studying your disease." The meta header had dystonia as the first keyword. This keyword was followed by nephrotic, vascular, and autonomic which isn't as important as dystonia. The other words the site uses is mitochondrial. ataxia is also included and could not be viewed by web crawlers.

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