The congress aims to bring together world leaders and young scientist from a variety of breaking through scientific field to present cutting edge research, to discuss results and to exchange ideas.
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Home - React-congress | raredisease-act.com Reviews
https://raredisease-act.com
The congress aims to bring together world leaders and young scientist from a variety of breaking through scientific field to present cutting edge research, to discuss results and to exchange ideas.
www.raredis.org
Registration of a rare disease patient. Access to treatment for rare diseases in Bulgaria. Epidemiological registries in Bulgaria. Orphan drugs in Bulgaria. 6th National Conference on Rare Diseases - 11-12 September 2015, Plovdiv (Bulgaria). This site complies with the HONcode standard for trustworthy health. Save the date for the Sixth National Conference for rare diseases and orphan drugs. Submission of proposals and request to the Commission on Rare Diseases. Last posts by topic. European Commission p...
Партнёры
По редким заболеваниям, "лекарствам - сиротам" и редко применяемым медицинским технологиям. Информация в СМИ о портале. Неотложная помощь при редких болезнях. Кодекс поведения (HONcode) для медицинских WEB-сайтов. WEB-сайт разделяет «Кодекс поведения (HONcode) для меди-. Цинских WEB-сайтов» The Health on the Net Foundation и планиру-. Ет проведение аккредитации и получение HONcode сертификата. АНТАГОНИСТЫ РЕЦЕПТОРОВ ЭНДОТЕЛИЯ ПРИ ЛЕГОЧНОЙ АРТЕРИАЛьНОЙ ГИПЕРТЕНЗИИ: ВЧЕРА, СЕГОДНЯ И ЗАВТРА. Научный конгрес...
rare disco records of the 1980s, home page
The story behind some of the best, the rarest and the downright bizarre Disco tunes. Raredisco.com will look closely at the early 1980s, a period when New York Disco and European New Wave mixed, mingled and bred some way-out records which laid the foundation for Electronic Dance Music as we know it. Feel free to browse the site. There is some sample content which might give you an idea of what's in store for you here. Would you like to know more? Tip Of The Month. Tip Of The Month.
Rarediscoveries.net
The domain rarediscoveries.net may be for sale. Click here for details.
rarediscus.com
Home - React-congress
International Congress on Research. Of Rare and Orphan Diseases. General terms and conditions. General terms and conditions.
raredisease-cme.org
Raredisease-cme.org is not available due to technical maintenance. Raredisease-cme.org is niet beschikbaar i.v.m. technisch onderhoud. 13-8-2015 • raredisease-cme.org.
Home - React-congress
International Congress on Research. Of Rare and Orphan Diseases. General terms and conditions. General terms and conditions.
CTOD-Clinical Trial Outcome Database
Clinical Trial Outcome Database - CTOD. One billion people suffer from one or more neglected infectious diseases - diseases that have historically attracted little investment to develop treatment, prevention, or control methods and that disproportionally affect the world's poorest and most vulnerable people. Effective treatment and control methods are available to fight many of these diseases, but significant progress cannot be made without more funding for drug delivery and better diagnostic tools t...
Raredisease-NI
Histio Spread The Word Find A Cure. Histiocytosis Find A Cure. Saturday, November 17, 2012. Consultation on the United Kingdom Plan For Rare Disease Northern Ireland. The Cavan Tommy Hoey Trust is shocked by the lack of responses to the United Kingdom Rare Disease Plan Northern Ireland Parties had the chance to give their views on how they see Rare Disease in Northern Ireland they failed the people in No. Northern Irland has and is falling short in health care of rare diseases and this is transferring th...
Seltene Erkrankungen Salzburg
Die Erforschung seltener Erkrankungen und die damit verbundene Patientenbetreuung brauchen besondere Anforderungen. Mehr als 7.000 verschiedene seltene Krankheiten wurden bisher identifiziert, die das tägliche Leben von mehr als 30 Millionen Menschen allein in Europa direkt betreffen. In Salzburg findet der von der EU ins Leben gerufene Aktionstag jedes Jahr unter dem Motto. Bdquo;Gemeinsam für Selten“. Statt Von seltenen Erkrankungen spricht man, wenn davon weniger als 1 von 2000 Menschen betroffen sind.
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