Angelman Syndrome Foundation, Inc. Research, Genetic Counseling, Diagnosis, Seizures, Angelmans Syndrome Association - Angelman 2

Angelman Syndrome Foundation, Inc The Angelman Syndrome Foundations mission is to advance the awareness and treatment of Angelman Syndrome through education and information, research, and support for individuals with Angelman Syndrome, their families and other concerned parties.

OVERVIEW

The web site angelman.org currently has a traffic ranking of zero (the smaller the better). We have inspected twelve pages inside the site angelman.org and found eight hundred and fifty-two websites referencing angelman.org. I found two contacts and addresses for angelman.org to help you connect with them. I found six social network accounts acquired by angelman.org. The web site angelman.org has been on the internet for one thousand three hundred and two weeks, fourteen days, fifty-seven minutes, and forty seconds.
Pages Crawled
12
Links to this site
852
Contacts
2
Addresses
2
Social Links
6
Online Since
Jul 1999

ANGELMAN.ORG TRAFFIC

The web site angelman.org has seen a alternation amounts of traffic all through the year.
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ANGELMAN.ORG HISTORY

The web site angelman.org was created on July 24, 1999. It is currently one thousand three hundred and two weeks, fourteen days, fifty-seven minutes, and forty seconds old.
REGISTERED
July
1999

WEBPAGE AGE

24
YEARS
11
MONTHS
12
DAYS

LINKS TO DOMAIN

Access 7 Online

How can we help you? Take a look inside. We strive to create a positively positive experience in special education. We strongly believe in supporting a Collaborative learning community, and promote the team approach. Proud Sponsors Of LIASEA and NYSOTA and Partners Of MSB. Approved Continuing Education Providers of. Access 7 Services, Inc. Sign Up for our Email Newsletter.

Agilis Homepage - Agilis Website

Agilis is advancing innovative DNA therapeutics designed to provide long-term efficacy for patients with debilitating, often fatal, rare genetic diseases that affect the central nervous system.

Family Blog

Monday, April 6, 2015. We are Glorified by Love.

News - Angelman Verein Schweiz

Wir informieren, beraten und unterstützen Eltern, Angehörige und Freunde von Menschen mit dem Angelman-Syndrom. Schön, dass Du da bist! Angelman Today Mai-Juni Ausgabe. Die neuste Ausgabe des Angelman Today. Viel Spass beim Lesen! Euer Angelman Verein Schweiz. Für den Angelman Verein an den GP Bern 2015.

Canadian Angelman Syndrome Society CASS

My child just got diagnosed with AS Now What. 2015 Calgary Marathon Please make Canadian Angelman Syndrome Society your Support Charity at the Run! Scotiabank Calgary Marathon Join us for the 51st running of the Calgary Marathon on May 31, 2015. Angelman Syndrome at a Glance.

WHAT DOES ANGELMAN.ORG LOOK LIKE?

Desktop Screenshot of angelman.org Mobile Screenshot of angelman.org Tablet Screenshot of angelman.org

CONTACTS

Angelman Syndrome Foundation Inc

Eileen Braun

4255 Westbrook Dr Ste 219

Aurora, IL, 60504

US

Angelman Syndrome Foundation,

Angelman Syndrome Foundation,

3015 E. New York Street, Suite

Aurora, IL, 60504

US

ANGELMAN.ORG SERVER

Our parsers detected that the main page on angelman.org took six hundred and fifty-five milliseconds to stream. I could not discover a SSL certificate, so our crawlers consider angelman.org not secure.
Load time
0.655 secs
SSL
NOT SECURE
Internet Protocol
64.154.105.13

NAME SERVERS

ns21.worldnic.com
ns22.worldnic.com

SERVER OS AND ENCODING

We found that this website is implementing the Microsoft-IIS/7.5 server.

HTML TITLE

Angelman Syndrome Foundation, Inc. Research, Genetic Counseling, Diagnosis, Seizures, Angelmans Syndrome Association - Angelman 2

DESCRIPTION

Angelman Syndrome Foundation, Inc The Angelman Syndrome Foundations mission is to advance the awareness and treatment of Angelman Syndrome through education and information, research, and support for individuals with Angelman Syndrome, their families and other concerned parties.

PARSED CONTENT

The web site angelman.org states the following, "Genetic Mechanisms of Angelman Syndrome." We noticed that the website said " Has someone in your family been recently diagnosed with Angelman syndrome? Fill out this simple form if you would like to receive more information on AS." It also said " 1 Million for Angelman Syndrome Research. Please take a moment to tell us about your interest in Angelman syndrome research. 2015 Hope Inspired Conference- July." The header had Angelman as the highest ranking optimized keyword. This keyword is followed by Angelman cure, Angelman disease, and Angelman disorder which isn't as urgent as Angelman. The other words angelman.org used was Angelman research. Angelman Syndrome is included but could not be viewed by search parsers.

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