ehdn.org

European Huntingtons Disease Network Advancing Research, Conducting Trials, Improving Care

NEWS EVENTS. HD Patients and Families. HD Patients and Families Home. Finding Clinics and Support. HD Clinicians and Researchers. HD Clinicians and Researchers Home. Previous Ongoing Research. Rater training and certification. Clinical Trial Sponsors Home. HD Clinical Trial Site Certification Scheme. Previous Ongoing Research. Resources, Services, and Accomplishments. News Events. European Huntingtons Disease Network. HD Patients and Families. Patients and Families Home. LEARN MORE ABOUT EHDN.
traffic

OVERVIEW

This web site ehdn.org presently has a traffic classification of zero (the smaller the better). We have researched fifteen pages inside the web page ehdn.org and found seven websites interfacing with ehdn.org.
Pages Analyzed
15
Links to this site
7

EHDN.ORG RANKINGS

This web site ehdn.org is seeing alternating quantities of traffic all over the year.
Traffic for ehdn.org

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Traffic ranking (by month) for ehdn.org

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LINKS TO BUSINESS

At Risk for Huntingtons Disease

The final result is a slow, ugly death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment. The best news for the Huntingtons disease communi. HD Free with PGD! .

About European Huntingtons Disease Network

We are happy to announce that EHDN has a new public face. Please visit us at www. Find information based on your background as clinician, researcher, HD family member or sponsor. On this website you can still access the. For all other things please visit the EHDN webpage. Has been moved to the HD Training Platform. This is immediately accessible for Enroll-HD site staff, and after an Application. For a User Account to others.

Home - Vereniging van Huntington

De weg naar kwaliteit van leven. Er is in de ruim veertig jaar dat de Vereniging nu bestaat, heel veel bereikt op het gebied van wetenschappelijk onderzoek, zorg, expertise, ervaringsdeskundigheid en voorlichting.

Witamy - Polskie Stowarzyszenie Choroby Huntingtona

Konferencja i XXIV Zjazd Członków Stowarzyszenia, 24 - 25 marca 2018, Warszawa. Budujemy bazę wiedzy o chorobie Huntingtona. dziedziczenia, diagnostyki, leczenia, życia z chorobą Huntingtona oraz troski o opiekunów chorych. Niezwykły dokument o spotkaniu pary przyjaciół. Marta jest dawną hippiską, Wojtek jest aktorem, tłumaczem i nauczycielem, który choruje na pląsawicę Huntingtona. Sprawdź, jak Ty możesz pomóc.

WHAT DOES EHDN.ORG LOOK LIKE?

Desktop Screenshot of ehdn.org Mobile Screenshot of ehdn.org Tablet Screenshot of ehdn.org

EHDN.ORG HOST

Our web crawlers caught that a lone root page on ehdn.org took one thousand four hundred and sixty-nine milliseconds to download. We could not observe a SSL certificate, so in conclusion I consider this site not secure.
Load time
1.469 seconds
SSL
NOT SECURE
Internet Address
162.13.78.10

SERVER OPERATING SYSTEM AND ENCODING

I revealed that this domain is operating the Apache/2.2.15 (Red Hat) os.

TITLE

European Huntingtons Disease Network Advancing Research, Conducting Trials, Improving Care

DESCRIPTION

NEWS EVENTS. HD Patients and Families. HD Patients and Families Home. Finding Clinics and Support. HD Clinicians and Researchers. HD Clinicians and Researchers Home. Previous Ongoing Research. Rater training and certification. Clinical Trial Sponsors Home. HD Clinical Trial Site Certification Scheme. Previous Ongoing Research. Resources, Services, and Accomplishments. News Events. European Huntingtons Disease Network. HD Patients and Families. Patients and Families Home. LEARN MORE ABOUT EHDN.

CONTENT

This web site states the following, "HD Patients and Families Home." Our analyzers noticed that the web page stated " HD Clinicians and Researchers Home." The Website also said " HD Clinical Trial Site Certification Scheme. Resources, Services, and Accomplishments."

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